SlideShare a Scribd company logo
Hindawi Publishing Corporation 
Infectious Diseases in Obstetrics and Gynecology 
Volume 2012, Article ID 628362, 9 pages 
doi:10.1155/2012/628362 
Research Article 
A First Look at ChorioamnionitisManagement Practice 
Variation among US Obstetricians 
Mara B. Greenberg,1 Britta L. Anderson,2 Jay Schulkin,2 
Mary E. Norton,1 and Natali Aziz1 
1Division of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, Lucile Packard Children’s 
Hospital at Stanford, Stanford University, 300 Pasteur Drive HH333, Stanford, CA 94305, USA 
2Department of Research, American College of Obstetricians and Gynecologists, P.O. Box 70620, Washington, WA 20024, USA 
Correspondence should be addressed toMara B. Greenberg, mbgreenberg@yahoo.com 
Received 21 August 2012; Accepted 26 November 2012 
Academic Editor: Catalin S. Buhimschi 
Copyright © 2012 Mara B. Greenberg et al. This is an open access article distributed under the Creative Commons Attribution 
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly 
cited. 
Objective. To examine practice patterns for diagnosis and treatment of chorioamnionitis among US obstetricians. Study Design.We 
distributed a mail-based survey to members of the American College of Obstetricians and Gynecologists, querying demographics, 
practice setting, and chorioamnionitis management strategies. We performed univariable and multivariable analyses. Results. Of 
500 surveys distributed, 53.8% were returned, and 212 met study criteria and were analyzed. Most respondents work in group 
practice (66.0%), perform >100 deliveries per year (60.0%), have been in practice >10 years (77.3%), and work in a nonuniversity 
setting (85.1%). Temperature plus one additional criterion (61.3%) was the most common diagnostic strategy. Over 25 different 
primary antibiotic regimens were reported, including use of a single agent by 30.0% of respondents. A wide range of postpartum 
antibiotic duration was reported from no postpartum treatment (34.5% after vaginal delivery, 11.3% after cesarean delivery) to 
48 hours of postpartum treatment (24.7% after vaginal delivery, 32.1% after cesarean delivery). No practitioner characteristic was 
independently associated with diagnostic or therapeutic strategies in multivariable analysis. Conclusion. There is a wide variation 
in contemporary clinical practices for the management of chorioamnionitis. This may represent a dearth of level I evidence. 
Future prospective clinical trials may provide more evidence-based practice recommendations for diagnosis and treatment of 
chorioamnionitis. 
1. Introduction 
Chorioamnionitis, infection of the amniotic fluid, mem-branes, 
placenta, and/or decidua, is a common intrapartum 
complication, affecting up to 10% of women during labor in 
the USA [1–6]. Potentially serious adverse maternal sequelae 
of chorioamnionitis include increased risk of operative 
delivery, postpartum hemorrhage, and postdelivery infection 
[1, 6–8]. Neonatal risks include sepsis and potential long-term 
consequences such as cerebral palsy [6–12]. The patho-genesis 
of chorioamnionitis is thought to be polymicrobial 
and involves bacteria that colonize the vagina including 
Gram-negative organisms and anaerobes. When chorioam-nionitis 
is suspected based on clinical findings prior to 
delivery, administration of broad spectrum antibiotics has 
been shown to be effective in reducing maternal and fetal 
morbidity and mortality [1–6, 9]. 
Which diagnostic and therapeutic strategies are associ-ated 
with optimalmaternal and neonatal outcomes is unclear 
due to a dearth of prospective randomized trials comparing 
various management strategies [1–6, 13]. Clinical chorioam-nionitis 
is traditionally diagnosed based on elevatedmaternal 
temperature associated with additional findings including 
maternal tachycardia, fetal tachycardia, maternal leuko-cytosis, 
uterine tenderness, and purulent amniotic fluid 
[1–6]. Number and type of diagnostic criteria associated 
with least maternal and neonatal morbidity have not been 
evaluated in a systematic fashion.Much of the peer-reviewed 
literature on chorioamnionitis either lacks a description of 
formal diagnostic criteria or reports utilization of elevated
2 Infectious Diseases in Obstetrics and Gynecology 
temperature plus two additional criteria [1–5, 8]. With 
regard to evidence-based treatment, though randomized 
and observational trials have demonstrated a reduction in 
neonatal sepsis with intrapartum rather than postpartum 
treatment for chorioamnionitis, there have been few head 
to head comparisons of different intrapartum regimens 
[14–17]. In contrast, several studies have demonstrated 
similar efficacy among different durations of postpartum 
therapy, with regard to resolution of maternal infection and 
development of postoperative infectious complications [18– 
21]. 
Likely due to limitations in the breadth of available 
data, guidelines are lacking regarding necessary clinical and 
laboratory diagnostic criteria, optimal antibiotic regimens, 
and duration of therapy. As a result of this uncertainty, 
practice patterns are likely to vary, potentially significantly. 
We hypothesized that obstetric care providers have a wide 
variety of practice patterns with regard to management 
of intrapartum chorioamnionitis. Identification of such 
variations in practice would allow us to target areas in which 
future investigation could be useful. In addition, for those 
aspects of chorioamnionitis management for which high 
quality data are available, it would be useful to define areas in 
which enhanced provider education regarding best practices 
might be beneficial. The purpose of this study was to deter-mine 
the current practice patterns among obstetricians in the 
USA regarding chorioamnionitis management strategies.We 
also examined provider characteristics associated with the 
use of different diagnostic and therapeutic practices. 
2.Materials andMethods 
Questionnaires were mailed in January 2011 to 500 Fellows 
and Junior Fellows of the American College of Obstetricians 
and Gynecologists (ACOG). The potential participants were 
members of the Collaborative Ambulatory ResearchNetwork 
(CARN), a consortium established to facilitate assessment 
of clinical practice patterns. CARN is comprised of 1200 
practicing obstetrician gynecologists who have volunteered 
to participate in 3–5 survey studies each year. 
The pool of potential participants was quasi randomly 
selected from the total CARN membership. The entire 
CARN sample pool was divided into groups of 100, all 
of which were similar with regard to mean age, gender, 
and ACOG district distribution. Five groups of 100 were 
then randomly chosen for this study sample. Each potential 
participant was assigned an identification number that was 
used to track the respondent while maintaining anonymity. 
A cover letter was included with the questionnaire, orienting 
survey recipients to the study and indicating a response 
deadline of approximately 3 weeks from the mailing date. 
Mailings also included postage paid return envelopes with 
the recipient identification number. All non-respondents 
received a second mailing of the questionnaire 5 weeks after 
the first mailing. A final mailing was sent approximately 
5 weeks later. Questionnaires returned by July 2011 were 
included in the study. The survey consisted of 27 questions 
including 7 demographic, 9 on practice characteristics, 6 on 
chorioamnionitis diagnostic practices, and 5 on treatment 
practices. Question formats includedmultiple choice, yes/no, 
and Likert response scale.We conducted a pilot survey of 157 
physicians and certified nurse midwives in June 2010 and 
utilized the results to eliminate ambiguity and redundancy 
in the questionnaire content and format. A sample of the 
questions on diagnostic and treatment strategies is listed in 
Table 1. 
Student’s t-tests were used to compare group means 
of continuous variables. Differences in categorical measures 
were assessed using Chi-squared test. Multivariable logistic 
regression analyses were used to control for potential con-founders 
in assessing differences between groups. For the 
multivariable models, we utilized four predictor variables 
thought to be clinically important, regardless of significance 
in univariable analysis: region of practice, number of years in 
practice, practice volume, and practice setting. We analyzed 
data using R version 2.11.1 (2010-05-31, The R Foundation 
for Statistical Computing). We considered a two-sided 
alpha of <0.05 to be significant. Institutional review board 
exemption was granted at Stanford University. 
3. Results and Discussion 
3.1. Results. Of the 500 surveys distributed, 269 were return-ed 
for a 53.8% response rate. Forty were excluded due to 
insufficient survey completion and 17 because the respon-dents 
reported that they do not currently practice inpatient 
obstetrics. The remaining 212 completed surveys were 
included in the analysis. Participants represent 42 different 
US states, Canada (3 providers) and Bahamas (1 provider), 
with female and male providers equally represented and 
a median provider age of 51 (Table 2). The majority of 
providers work in private or community practice (83.2%), 
have been in practice greater than 10 years (77.3%), and 
perform over 100 deliveries per year (60.0%) (Table 2). 
Table 3 shows diagnostic management practices. Most 
providers reported using temperature plus one additional 
criterion for diagnosis of chorioamnionitis (61.3%), with 
the most common temperature threshold being 38.0 degrees 
Centigrade. The majority of providers use interventions to 
attempt to lower maternal temperature prior to making 
the diagnosis of chorioamnionitis (69.0%), including 7.1% 
who administer acetaminophen for this purpose prior to 
diagnosis. The presence of epidural analgesia influences 
the likelihood of diagnosing chorioamnionitis for 41.2% 
of providers, and 9.0% are influenced by their institution’s 
neonatal sepsis workup policy. 
Responses about treatment practices are shown in 
Table 3. Respondents listed over 25 different antibiotic reg-imens 
as their primary choice for treating chorioamnionitis. 
A regimen containing ampicillin and gentamicin is used by 
65.3% of providers, while 30.0% of respondents use a single-agent 
regimen. A regimen without Gram-negative coverage, 
either ampicillin alone or cefazolin alone, is used by 14.5% 
of providers. A wide range of duration of postpartum antibi-otic 
therapy was reported from no postpartum treatment 
(34.5% after vaginal delivery, 11.3% after cesarean delivery)
Infectious Diseases in Obstetrics and Gynecology 3 
Table 1: Questions on diagnostic and treatment strategies. 
Describe your most common strategy for diagnosing intrapartum chorioamnionitis. 
 Elevated temperature alone 
 Elevated temperature plus at least one additional sign or symptom 
 Elevated temperature plus at least two additional signs or symptoms 
 At least one sign or symptom alone without elevated temperature 
 Other: 
What temperature is your threshold for diagnosing intrapartum chorioamnionitis? 
 37.8◦C (100.0◦F) 
 37.9◦C (100.2◦F) 
 38.0◦C (100.4◦F) 
 38.1◦C (100.6◦F) 
 38.2◦C (100.8◦F) 
 Other: 
What strategies do you use to lower maternal temperature before deciding whether a patient meets diagnostic criteria for 
chorioamnionitis? Choose all that apply. 
 None 
 IV fluid bolus 
 PO hydration 
 Tylenol or other antipyretics 
 External cooling (application of ice or cool cloths) 
 Other: 
If a patient has a fever alone, with no additional signs or symptoms of chorioamnionitis, is it likely that your decision to treat for 
chorioamnionitis would be influenced by whether the patient has an epidural? 
 No 
 Yes, I would be more likely to diagnose chorioamnionitis and treat accordingly in a patient with a fever and an epidural than one 
without an epidural 
 Yes, I would be less likely to diagnose chorioamnionitis and treat accordingly in a patient with a fever and an epidural than one 
without an epidural 
Do you think your institution’s policy on neonatal sepsis workup influences how frequently you diagnose maternal chorioamnionitis? 
 No 
 Yes, I am more likely to diagnose maternal chorioamnionitis because of my institution’s policy on neonatal sepsis workup 
 Yes, I am less likely to diagnose maternal chorioamnionitis because of my institution’s policy on neonatal sepsis workup 
What is the most common antibiotic regimen you use for treating intrapartum chorioamnionitis?∗ 
 Ampicillin 
 Azithromycin 
 Ancef (Cefazolin) 
 Cefotetan 
 Cefoxitin 
 Clindamycin 
 Ertapenem 
 Gentamicin, daily dosing 
 Gentamicin, TID dosing 
 Metronidazole 
 Unasyn (Ampicillin/sulbactam) 
 Zosyn (Piperacillin/tazobactam)
4 Infectious Diseases in Obstetrics and Gynecology 
Table 1: Continued. 
 Ampicillin plus Gentamicin, daily dosing 
 Ampicillin plus Gentamicin, TID dosing 
 Ampicillin plus Gentamicin daily dosing plus Clindamycin 
 Ampicillin plus Gentamicin TID dosing plus Clindamycin 
 Other: 
What is the most common antibiotic regimen you use for treating intrapartum chorioamnionitis in the setting of cesarean delivery?∗ 
 Same regimen as above 
 Different regimen (please check all that apply): 
 Ampicillin 
 Azithromycin 
 Ancef (Cefazolin) 
 Cefotetan 
 Cefoxitin 
 Clindamycin 
 Ertapenem 
 Gentamicin, daily dosing 
 Gentamicin, TID dosing 
 Metronidazole 
 Unasyn (Ampicillin/sulbactam) 
 Zosyn (Piperacillin/tazobactam) 
 Ampicillin plus Gentamicin, daily dosing 
 Ampicillin plus Gentamicin, TID dosing 
 Ampicillin plus Gentamicin daily dosing plus Clindamycin 
 Ampicillin plus Gentamicin TID dosing plus Clindamycin 
 Other: 
What is your strategy for postpartum treatment after a vaginal delivery, in women diagnosed with intrapartum chorioamnionitis, in 
the absence of endometritis? 
 No additional antibiotics after delivery 
 One additional dose of antibiotics after delivery 
 Continue antibiotics for 24 hours after delivery 
 Continue antibiotics for 48 hours after delivery 
 Continue antibiotics for 24 hours after last fever 
 Continue antibiotics for 48 hours after last fever 
 Other: 
What is your strategy for postpartum treatment after a cesarean delivery, in women diagnosed with intrapartum chorioamnionitis, in 
the absence of endometritis? 
 No additional antibiotics after delivery 
 One additional dose of antibiotics after delivery 
 Continue antibiotics for 24 hours after delivery 
 Continue antibiotics for 48 hours after delivery 
 Continue antibiotics for 24 hours after last fever 
 Continue antibiotics for 48 hours after last fever 
 Other:
Infectious Diseases in Obstetrics and Gynecology 5 
Table 1: Continued. 
Do you treat with oral antibiotics after a patient has finished her postpartum course of IV antibiotics? 
 Yes 
 No 
∗Responses were not limited to one of the choices listed but rather one or more than one antibiotic choice as needed to accurately reflect respondents’ primary 
regimen. 
to 48 hours of postpartum treatment (24.7% after vaginal 
delivery, 32.1% after cesarean delivery). Sixteen percent of 
providers utilize oral antibiotics after completion of the 
intravenous regimen. 
We examined the relationship between management 
strategies and the following provider characteristics: region 
of practice, length of time in practice, practice setting, and 
practice volume. In univariable analysis, university-based 
practitioners were less likely to report use of single-agent 
regimen (13.8% versus 32.6%, P = 0.04) and more likely 
to report sufficient Gram-negative coverage (100% versus 
83.4%, P = 0.02) when compared to non-university-based 
practitioners. Those in practice for 10 years were more 
likely to report using a regimen with sufficient Gram-negative 
coverage than those in practice for 10 years (97.8% 
versus 82.0%, P = 0.007) and less likely to prescribe a 
course of oral antibiotics after completion of the intravenous 
course (8.3% versus 24.7%, P = 0.01). Region of practice 
was associated with likelihood of reporting use of ≤1 dose of 
additional antibiotics after vaginal delivery compared with 
1 dose with more providers from the Midwest treating 
with ≤1 antibiotic dose (67.9%) compared to providers from 
other regions (west 46.7%, south 36.2%, northeast 26.3%, 
P  0.001). No other provider characteristics were associated 
with differences in management strategy in univariable anal-ysis 
(data not shown). In multivariable logistic regression 
analysis controlling for the practice volume, region, setting, 
and length of time in practice, no provider characteristics 
were independently statistically significantly associated with 
differences in any chorioamnionitis management strategy. 
3.2. Discussion. We demonstrate a wide variation in prac-tice 
patterns for management of chorioamnionitis among 
obstetric care providers in the USA.We identified significant 
heterogeneity in essentially all aspects of management, 
including criteria for diagnosis, influences on likelihood of 
making the diagnosis, choice of antibiotics, and type and 
duration of postpartum treatment. 
This wide variety of diagnostic and treatment strategies 
is likely in part due to a dearth of high-quality clinical 
data to guide practice and indicates a need for further 
investigation into optimal strategies for the management of 
chorioamnionitis. For example, 60% of obstetricians require 
elevated temperature plus one additional criterion when 
making the diagnosis of chorioamnionitis, and a quarter of 
clinicians use elevated temperature alone. The latter strategy 
likely results in more patients being diagnosed with and 
treated for intrapartum infection than strategies that require 
additional signs or symptoms. Whether or not this lower 
threshold for diagnosis of chorioamnionitis is associated 
with fewer adverse outcomes is unclear and deserves further 
study. 
Over two-thirds of providers utilize strategies to attempt 
to lower maternal temperature prior to making a diagnosis 
of chorioamnionitis. This may represent uncertainty by 
obstetricians regarding whether treatment in the setting 
of elevated temperature alone is associated with optimal 
outcomes, as well as acknowledgement that there are a 
variety of influences on maternal temperature in labor [1– 
6, 22–27]. As with other diagnostic criteria, there are no 
data regarding maternal or neonatal outcomes associated 
with initial management of maternal fever using intravenous 
fluids, acetaminophen, and/or external cooling prior to 
diagnosing chorioamnionitis and initiating antibiotics in 
labor. 
Sixty percent of providers do not consider the presence 
of epidural analgesia in the diagnosis of chorioamnionitis, 
while the remainder are influenced by presence of epidural 
in making diagnostic and treatment decisions. This hetero-geneity 
of management styles reflects the lack of consensus 
on best practices regarding the complex relationship between 
epidural, maternal fever, and neonatal outcomes, despite 
multiple publications addressing this issue [22–27]. While 
current literature suggests that elevated maternal temper-ature 
associated with epidural use is not associated with 
neonatal sepsis, a consensus regarding how presence of 
epidural should inform chorioamnionitis diagnostic thresh-old 
has yet to be reached [22–27]. 
The vast majority of obstetricians surveyed do not take 
their institution’s neonatal sepsis workup policy into account 
when diagnosing chorioamnionitis. However, of the 7% of 
providers who are influenced by such policies, more than 
two-thirds report that they are less likely to diagnose and 
treat clinically suspected chorioamnionitis as a result of 
their institution’s policy. Presumably this indicates a degree 
of uncertainty regarding the cost-benefit ratio of exposing 
neonates to invasive procedures, given the lack of an evident 
number needed to treat to prevent neonatal harm when the 
clinical diagnosis of chorioamnionitis is uncertain. 
A 2002 Cochrane Database Review indicated that there 
are insufficient data on which to base a recommendation 
for optimal antibiotic regimens in the setting of chorioam-nionitis 
[13]. Not surprisingly, our results demonstrate a 
wide variety of antibiotic regimens in common use. Most 
of these regimens contain sufficient Gram-negative coverage 
and consist of broad spectrumantibiotics that cover for beta-lactamase 
producing aerobes and anaerobes, as has been 
recommended by expert consensus and nonrandomized 
published studies [1–6, 9, 13–16, 22–27]. However, 15%
6 Infectious Diseases in Obstetrics and Gynecology 
Table 2: Respondent characteristics. 
Respondent characteristics N = 212 
Female 103 (48.8%) 
Male 109 (51.2%) 
Median age (IQR) 51 (43–60) 
Physician ethnicity 
Non-HispanicWhite 173 (82.0%) 
Other 38 (18.0%) 
Number of deliveries annually 
100 84 (40.0%) 
100 126 (60.0%) 
Region of USa 
West 46 (22.0%) 
Midwest 54 (25.8%) 
South 69 (33.0%) 
Northeast 38 (18.2%) 
Practice location 
Suburban 106 (50.2%) 
Urban 75 (35.5%) 
Rural 25 (11.8%) 
Other 5 (2.5%) 
Predominant patient insurance type 
Private 154 (73.3%) 
Public 55 (26.2%) 
Uninsured 1 (0.5%) 
Predominant patient ethnicity 
Non-HispanicWhite 148 (70.8%) 
HispanicWhite 32 (15.3%) 
Other 29 (13.9%) 
Years in practice 
0–5 5 (2.4%) 
6–10 43 (20.3%) 
11–15 43 (20.3%) 
16–20 25 (11.8%) 
21–25 34 (16.0%) 
26–30 27 (12.7%) 
30 35 (16.5%) 
Practice setting 
Private or community 174 (83.2%) 
University or academic 29 (13.9%) 
Government 5 (2.4%) 
Other 1 (0.5%) 
Practice type 
Obgyn partnership/group 140 (66.0%) 
University/teaching institution 26 (12.3%) 
Solo practice 38 (17.9%) 
Laborist/hospitalist 0 
Other 8 (3.8%) 
aLocation of practice divided into four regions for purposes of analysis, 
according to the Centers for Disease Control and Prevention “Geographic 
Regions of the United States,” http://www.cdc.gov/. 
of providers use ampicillin or cefazolin alone, regimens that 
do not contain Gram-negative coverage and are theoret-ically 
insufficient for covering the spectrum of microbes 
commonly seen with chorioamnionitis. We found that use 
of a regimen with insufficient Gram-negative coverage is 
associated with practice type and duration, with community 
physicians and those in practice for 10 years more likely 
to use such a regimen than those in university practice and 
more recently in training. 
While use of a single agent appears to be common 
practice (30% of respondents), no studies have compared the 
use of a single agent to a multidrug regimen for treatment of 
chorioamnionitis. Use of a single agent is also associated with 
practice type, with fewer physicians in university practice 
reporting use of a single agent as compared to those in 
community practice. These discrepancies may be indicative 
of variation in management styles between university and 
community practices. 
Several studies have investigated the association between 
duration of postpartum therapy, resolution of maternal 
infection, and development of postoperative infectious 
complications [18–21]. While randomized trials have not 
demonstrated a difference in efficacy between “traditional” 
24–48 hour postpartum courses and “abbreviated” courses 
consisting of ≤1 postpartum dose of antibiotics, the majority 
of providers continue to use 24–48 hour courses. Unlike 
other practice patterns studied, region of practice but not 
practice type is associated with likelihood of adopting an 
abbreviated postpartum antibiotic course.Whilemost obste-tricians 
do not use oral antibiotic therapy after completion 
of an intravenous postpartum course, a significant minority 
(16%) uses oral antibiotics to complete a longer treatment 
course. This practice is in contrast with randomized data 
demonstrating lack of benefit of such a strategy [28]. 
While this study describes clear differences in the 
management of chorioamnionitis amongst a diverse group 
of obstetric providers, it is not without limitations. These 
include a relatively small sample size, which may decrease 
our ability to detect potential differences in management 
practices attributable to variability in provider character-istics. 
Similarly, our findings may not be generalizable to 
practitioners outside of the ACOG membership and the 
demographic included. The response rate of 54% may have 
led to nonresponse bias, though this is near the upper end 
of the 35%–60% response rate typical of previous ACOG 
surveys [29, 30]. Additionally among those surveyed, a wide 
variety of practice settings and geographic regions were 
represented. Due to the constraints of a postal-based survey 
strategy, we were also limited in our ability to capture more 
comprehensive details about chorioamnionitis management 
strategies and their associated outcomes or about the risk 
profiles of respondent’s patient populations. Many providers 
likely have a more nuanced approach to the diagnosis and 
treatment of chorioamnionitis than can be appreciated based 
on the brief closed-ended survey approach employed. 
4. Conclusions 
This study is the first to report on chorioamnionitis man-agement 
patterns among US obstetricians. The heterogeneity 
of practice patterns we demonstrate has several potential 
implications. Many aspects of variation in management
Infectious Diseases in Obstetrics and Gynecology 7 
Table 3: Diagnostic and treatment strategies. 
Diagnostic strategies N = 212 
Diagnosis based on 
Temperature alone 56 (26.4%) 
Temperature plus one additional criterion 130 (61.3%) 
Temperature plus two additional criteria 16 (7.6%) 
Other 10 (4.7%) 
Most common temperature threshold (degrees Centigrade) 
37.9 6 (2.8%) 
38.0 154 (73.0%) 
38.1 23 (10.9%) 
38.2 18 (8.5%) 
Other 10 (4.7%) 
Strategies used to lower temperature prior to diagnosis 
None 65 (31.0%) 
Intravenous fluids 124 (59.0%) 
Acetaminophen 15 (7.1%) 
Other 6 (2.9%) 
Influenced by presence of epidural in making diagnosis 
No 124 (58.8%) 
More likely to diagnose 10 (4.7%) 
Less likely to diagnose 77 (36.5%) 
Neonatal sepsis workup required for all chorioamnionitis diagnoses 
Yes 170 (83.3%) 
No 34 (16.7%) 
Influenced by neonatal sepsis workup policy in making diagnosis 
No 191 (91.0%) 
More likely to diagnose 5 (2.3%) 
Less likely to diagnose 14 (6.7%) 
Treatment Strategies N = 212 
Primary treatment regimen 
Ampicillin and gentamicin ± additional agent 135 (65.2%) 
Single agent 62 (30.0%) 
Includes Gram-negative coverage 177 (85.5%) 
Does not include Gram-negative coverage 30 (14.5%) 
Change regimens for cesarean delivery 
Yes 99 (46.9%) 
No 112 (53.1%) 
Postpartum treatment strategy after vaginal delivery 
No additional antibiotics 73 (34.6%) 
1 additional dose 20 (9.5%) 
24 hours postpartum 56 (26.5%) 
24 hours afebrile 3 (1.4%) 
48 hours postpartum 52 (24.7%) 
48 hours afebrile 4 (1.9%) 
Other 3 (1.4%) 
Postpartum treatment strategy after cesarean delivery 
No additional antibiotics 24 (11.3%) 
1 additional dose 15 (7.1%) 
24 hours postpartum 70 (33.0%)
8 Infectious Diseases in Obstetrics and Gynecology 
Table 3: Continued. 
24 hours afebrile 17 (8.0%) 
48 hours postpartum 68 (32.1%) 
48 hours afebrile 16 (7.6%) 
Other 2 (0.9%) 
Treat with oral antibiotics after intravenous course completed 
Yes 34 (16.2%) 
No 176 (83.8%) 
strategy may reasonably be thought to represent lack of high-quality 
data necessary to guide practice in a coherent fashion. 
These understudied aspects of care include number and type 
of diagnostic criteria, influence of epidural on diagnosis, 
and type of antibiotic regimen. While some heterogeneity in 
practice may be acceptable, such as in the use of numerous 
antibiotics that cover the same bacteria but have varying 
prices, availability, ease of use, and tolerability, studies deter-mining 
optimal maternal and neonatal outcomes associated 
with particular management strategies in these understudied 
areas may be helpful to inform best practices. Data regarding 
which strategies are associated with decreased rates of 
neonatal sepsis and improvements in long-term child health 
are important to guide providers in these areas as these are 
associated with the most current uncertainty.With regard to 
several management issues that have already been studied in 
randomized trials, such as duration and type of postpartum 
therapy, our results indicate that efforts should be made 
to increase dissemination of best practice guidelines across 
obstetric demographics. 
Acknowledgments 
This study was funded in part by Grant no UA6MC19010, 
through the Maternal and Child Health Research Programs, 
Health Resources and Services Adminstration, U.S. Depart-ment 
of Health and Human Services, presented at the Society 
forMaternal FetalMedicine 32nd AnnualMeeting, February 
6–11, 2012, Dallas, TX. 
References 
[1] A. T. N. Tita andW.W. Andrews, “Diagnosis andmanagement 
of clinical chorioamnionitis,” Clinics in Perinatology, vol. 37, 
no. 2, pp. 339–354, 2010. 
[2] L. C. Gilstrap III and S. M. Cox, “Acute chorioamnionitis,” 
Obstetrics and Gynecology Clinics of North America, vol. 16, no. 
2, pp. 373–379, 1989. 
[3] D. E. Soper, C. G. Mayhall, andH. P.Dalton, “Risk factors for 
intraamniotic infection: a prospective epidemiologic study,” 
American Journal of Obstetrics and Gynecology, vol. 161, no. 
3, pp. 562–566, 1989. 
[4] E. R. Newton, “Chorioamnionitis and intraamniotic infec-tion,” 
Clinical Obstetrics and Gynecology, vol. 36, no. 4, pp. 
795–808, 1993. 
[5] J. W. Riggs and J. D. Blanco, “Pathophysiology, diagnosis, 
and management of intraamniotic infection,” Seminars in 
Perinatology, vol. 22, no. 4, pp. 251–259, 1998. 
[6] R. K. Edwards, “Chorioamnionitis and labor,” Obstetrics and 
Gynecology Clinics of North America, vol. 32, no. 2, pp. 287– 
296, 2005. 
[7] J. C. Hauth, L. C. Gilstrap, G. D. V. Hankins, and K. D. 
Connor, “Term maternal and neonatal complications of acute 
chorioamnionitis,” Obstetrics and Gynecology, vol. 66, no. 1, 
pp. 59–62, 1985. 
[8] D. J. Rouse, M. Landon, K. J. Leveno et al., “The maternal-fetal 
medicine units cesarean registry: chorioamnionitis at 
term and its duration—relationship to outcomes,” American 
Journal of Obstetrics and Gynecology, vol. 191, no. 1, pp. 211– 
216, 2004. 
[9] R. S. Gibbs and P. Duff, “Progress in pathogenesis and man-agement 
of clinical intraamniotic infection,” American Journal 
of Obstetrics and Gynecology, vol. 164, no. 5 I, pp. 1317–1326, 
1991. 
[10] J. M. Alexander, D. M.McIntire, and K. J. Leveno, “Chorioam-nionitis 
and the prognosis for term infants,” Obstetrics and 
Gynecology, vol. 94, no. 2, pp. 274–278, 1999. 
[11] J. G. Shatrov, S. C. M. Birch, L. T. Lam, J. A. Quinlivan, S. 
McIntyre, and G. L. Mendz, “Chorioamnionitis and cerebral 
palsy: ameta-analysis,” Obstetrics and Gynecology, vol. 116, no. 
2, pp. 387–392, 2010. 
[12] N. Aziz, Y.W. Cheng, and A. B. Caughey, “Neonatal outcomes 
in the setting of preterm premature rupture of membranes 
complicated by chorioamnionitis,” Journal of Maternal-Fetal 
and Neonatal Medicine, vol. 22, no. 9, pp. 780–784, 2009. 
[13] L. Hopkins and F. Smaill, “Antibiotic regimens for man-agement 
of intraamniotic infection,” Cochrane Database of 
Systematic Reviews, no. 3, Article ID CD003254, 2002. 
[14] R. S. Sperling, R. S. Ramamurthy, andR. S. Gibbs, “A compari-son 
of intrapartum versus immediate postpartum treatment of 
intra-amniotic infection,” Obstetrics and Gynecology, vol. 70, 
no. 6, pp. 861–865, 1987. 
[15] R. S. Gibbs, M. J. Dinsmoor, E. R. Newton, and R. S. 
Ramamurthy, “A randomized trial of intrapartum versus 
immediate postpartum treatment of women with intra-amniotic 
infection,” Obstetrics and Gynecology, vol. 72, no. 6, 
pp. 823–828, 1988. 
[16] L. C. Gilstrap, K. J. Leveno, S. M. Cox, J. S. Burris, M. 
Mashburn, and C. R. Rosenfeld, “Intrapartum treatment of 
acute chorioamnionitis: impact on neonatal sepsis,” American 
Journal of Obstetrics and Gynecology, vol. 159, no. 3, pp. 579– 
583, 1988. 
[17] M. C. Maberry and L. C. Gilstrap, “Intrapartum antibiotic 
therapy for suspected intraamniotic infection: impact on the 
fetus and neonate,” Clinical Obstetrics and Gynecology, vol. 34, 
no. 2, pp. 345–351, 1991. 
[18] S. J. Chapman and J. Owen, “Randomized trial of single-dose 
versus multiple-dose cefotetan for the postpartum treatment 
of intrapartum chorioamnionitis,” American Journal of Obstet-rics 
and Gynecology, vol. 177, no. 4, pp. 831–834, 1997.
Infectious Diseases in Obstetrics and Gynecology 9 
[19] R. K. Edwards and P. Duff, “Single additional dose postpartum 
therapy for women with chorioamnionitis,” Obstetrics and 
Gynecology, vol. 102, no. 5, pp. 957–961, 2003. 
[20] M. A. Turnquest, H. Y. How, C. R. Cook et al., “Chorioam-nionitis: 
is continuation of antibiotic therapy necessary after 
cesarean section?” American Journal of Obstetrics and Gynecol-ogy, 
vol. 179, no. 5, pp. 1261–1266, 1998. 
[21] C. Berry, K. A. Hansen, and J. F. McCaul, “Abbreviated antibi-otic 
therapy for clinical chorioamnionitis: a randomized trial,” 
Journal of Maternal-Fetal Medicine, vol. 3, no. 5, pp. 216–218, 
1994. 
[22] B. L. Leighton and S.H.Halpern, “The effects of epidural anal-gesia 
on labor, maternal, and neonatal outcomes: a systematic 
review,” American Journal of Obstetrics and Gynecology, vol. 
186, no. 5, pp. S69–S77, 2002. 
[23] L. Goetzl, A. Cohen, F. Frigoletto Jr., J. M. Lang, and E. 
Lieberman, “Maternal epidural analgesia and rates ofmaternal 
antibiotic treatment in a low-risk nulliparous population,” 
Journal of Perinatology, vol. 23, no. 6, pp. 457–461, 2003. 
[24] O. Apantaku and V. Mulik, “Maternal intra-partum fever,” 
Journal of Obstetrics and Gynaecology, vol. 27, no. 1, pp. 12– 
15, 2007. 
[25] L. E. Riley, A. C. Celi, A. B.Onderdonk et al. et al., “Association 
of epidural-related fever and noninfectious inflammation in 
termlabor,” Obstetrics and Gynecology, vol. 117, no. 3, pp. 588– 
595, 2011. 
[26] E. Lieberman, J. M. Lang, F. Frigoletto Jr., D. K. Richardson, 
S. A. Ringer, and A. Cohen, “Epidural analgesia, intrapartum 
fever, and neonatal sepsis evaluation,” Pediatrics, vol. 99, no. 3, 
pp. 415–419, 1997. 
[27] F. A. de Orange, R. Passini Jr., M. M. Amorim, T. Almeida, 
and A. Barros, “Combined spinal and epidural anaesthesia and 
maternal intrapartum temperature during vaginal delivery: a 
randomized clinical trial,” British Journal of Anaesthesia, vol. 
107, no. 5, pp. 762–768, 2011. 
[28] M. J. Dinsmoor, E. R. Newton, and R. S. Gibbs, “A random-ized, 
double-blind, placebo-controlled trial of oral antibiotic 
therapy following intravenous antibiotic therapy for postpar-tum 
endometritis,” Obstetrics and Gynecology, vol. 77, no. 1, 
pp. 60–62, 1991. 
[29] D. M. Kissin, M. L. Power, E. B. Kahn et al., “Attitudes and 
practices of obstetrician-gynecologists regarding influenza 
vaccination in pregnancy,” Obstetrics and Gynecology, vol. 118, 
no. 5, pp. 1074–1080, 2011. 
[30] K. A. Matteson, B. L. Anderson, S. B. Pinto, V. Lopes, J. 
Schulkin, and M. A. Clark, “Practice patterns and attitudes 
about treating abnormal uterine bleeding: a national survey of 
obstetricians and gynecologists,” American Journal of Obstet-rics 
and Gynecology, vol. 205, no. 4, pp. 321.e1–321.e8, 2011.
MEDIATORS 
of 
INFLAMMATION 
Journal of 
Gastroenterology 
Research and Practice 
Submit your manuscripts at 
http://www.hindawi.com 
Stem Cells 
International 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014 
Behavioural 
Neurology 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014 
Disease Markers 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014 
International Journal of 
Endocrinology 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014 
BioMed 
Research International 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014 
Journal of 
Oncology 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014 
Oxidative Medicine and 
Cellular Longevity 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014 
The Scientific 
World Journal 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014 
Journal of 
Immunology Research 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014 
PPAR Research 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014 
Journal of 
Obesity 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014 
Journal of 
Ophthalmology 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014 
Computational and 
Mathematical Methods 
in Medicine 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014 
Diabetes Research 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014 
AIDS 
Research and Treatment 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014 
Evidence-Based 
Complementary and 
Alternative Medicine 
Hindawi Publishing Corporation 
http://www.hindawi.com 
Parkinson’s 
Disease 
Volume 2014 
Hindawi Publishing Corporation 
http://www.hindawi.com Volume 2014

More Related Content

What's hot

Obstetrics and gynecology outpatient scenario of an Indian homeopathic hospit...
Obstetrics and gynecology outpatient scenario of an Indian homeopathic hospit...Obstetrics and gynecology outpatient scenario of an Indian homeopathic hospit...
Obstetrics and gynecology outpatient scenario of an Indian homeopathic hospit...
home
 
Patient Recruitment in Clinical Trials
Patient Recruitment in Clinical TrialsPatient Recruitment in Clinical Trials
Patient Recruitment in Clinical Trials
Raymond Panas
 
International Journal of Reproductive Medicine & Gynecology
International Journal of Reproductive Medicine & GynecologyInternational Journal of Reproductive Medicine & Gynecology
International Journal of Reproductive Medicine & Gynecology
SciRes Literature LLC. | Open Access Journals
 
Natalie Duran - Publications-Abstracts
Natalie Duran - Publications-AbstractsNatalie Duran - Publications-Abstracts
Natalie Duran - Publications-AbstractsNatalie Duran
 
surgical nurses in teaching hospitals in Ireland understanding pain
surgical nurses in teaching hospitals in Ireland understanding painsurgical nurses in teaching hospitals in Ireland understanding pain
surgical nurses in teaching hospitals in Ireland understanding painNiamh Vickers
 
Journal Club Indian Journal Of Pharmacology
Journal Club Indian Journal Of PharmacologyJournal Club Indian Journal Of Pharmacology
Journal Club Indian Journal Of Pharmacology
Dr Ketan Asawalle
 
4. case control study
4. case control study4. case control study
4. case control study
Ashok Kulkarni
 
Cancer epi 5
Cancer epi 5Cancer epi 5
Cancer epi 5
yasserflaifal
 
Journal of Clinical Pharmacology & Biopharmaceutics
Journal of Clinical Pharmacology & BiopharmaceuticsJournal of Clinical Pharmacology & Biopharmaceutics
Journal of Clinical Pharmacology & Biopharmaceutics
OMICS International
 
Cullen Presentation
Cullen PresentationCullen Presentation
Cullen Presentationsggibson
 
Luisetto m, ghulam r m. intensive care units the clinical pharmacist role to ...
Luisetto m, ghulam r m. intensive care units the clinical pharmacist role to ...Luisetto m, ghulam r m. intensive care units the clinical pharmacist role to ...
Luisetto m, ghulam r m. intensive care units the clinical pharmacist role to ...
M. Luisetto Pharm.D.Spec. Pharmacology
 
The Effects of Nurse Staffing on Adverse Events, Morbidity, Mortality, and Me...
The Effects of Nurse Staffing on Adverse Events, Morbidity, Mortality, and Me...The Effects of Nurse Staffing on Adverse Events, Morbidity, Mortality, and Me...
The Effects of Nurse Staffing on Adverse Events, Morbidity, Mortality, and Me...
Healthcare consultant
 
A SYSTEMATIC REVIEW ON SELF-REPORTED QUESTIONNAIRES TO ASSESS MEDICATION ADH...
 A SYSTEMATIC REVIEW ON SELF-REPORTED QUESTIONNAIRES TO ASSESS MEDICATION ADH... A SYSTEMATIC REVIEW ON SELF-REPORTED QUESTIONNAIRES TO ASSESS MEDICATION ADH...
A SYSTEMATIC REVIEW ON SELF-REPORTED QUESTIONNAIRES TO ASSESS MEDICATION ADH...
Aji Wibowo
 
Recruitment Metrics from TogetherRA: A Study in Rheumatoid Arthritis Patients...
Recruitment Metrics from TogetherRA: A Study in Rheumatoid Arthritis Patients...Recruitment Metrics from TogetherRA: A Study in Rheumatoid Arthritis Patients...
Recruitment Metrics from TogetherRA: A Study in Rheumatoid Arthritis Patients...
John Reites
 
Measurement of outcomes in epidemiology
Measurement of outcomes in epidemiologyMeasurement of outcomes in epidemiology
Measurement of outcomes in epidemiology
Dr. Ankit Gaur
 

What's hot (20)

community ebp poster presentation
community ebp poster presentationcommunity ebp poster presentation
community ebp poster presentation
 
Obstetrics and gynecology outpatient scenario of an Indian homeopathic hospit...
Obstetrics and gynecology outpatient scenario of an Indian homeopathic hospit...Obstetrics and gynecology outpatient scenario of an Indian homeopathic hospit...
Obstetrics and gynecology outpatient scenario of an Indian homeopathic hospit...
 
Patient Recruitment in Clinical Trials
Patient Recruitment in Clinical TrialsPatient Recruitment in Clinical Trials
Patient Recruitment in Clinical Trials
 
International Journal of Reproductive Medicine & Gynecology
International Journal of Reproductive Medicine & GynecologyInternational Journal of Reproductive Medicine & Gynecology
International Journal of Reproductive Medicine & Gynecology
 
Natalie Duran - Publications-Abstracts
Natalie Duran - Publications-AbstractsNatalie Duran - Publications-Abstracts
Natalie Duran - Publications-Abstracts
 
surgical nurses in teaching hospitals in Ireland understanding pain
surgical nurses in teaching hospitals in Ireland understanding painsurgical nurses in teaching hospitals in Ireland understanding pain
surgical nurses in teaching hospitals in Ireland understanding pain
 
Journal Club Indian Journal Of Pharmacology
Journal Club Indian Journal Of PharmacologyJournal Club Indian Journal Of Pharmacology
Journal Club Indian Journal Of Pharmacology
 
4. case control study
4. case control study4. case control study
4. case control study
 
Cancer epi 5
Cancer epi 5Cancer epi 5
Cancer epi 5
 
Journal of Clinical Pharmacology & Biopharmaceutics
Journal of Clinical Pharmacology & BiopharmaceuticsJournal of Clinical Pharmacology & Biopharmaceutics
Journal of Clinical Pharmacology & Biopharmaceutics
 
Cullen Presentation
Cullen PresentationCullen Presentation
Cullen Presentation
 
Luisetto m, ghulam r m. intensive care units the clinical pharmacist role to ...
Luisetto m, ghulam r m. intensive care units the clinical pharmacist role to ...Luisetto m, ghulam r m. intensive care units the clinical pharmacist role to ...
Luisetto m, ghulam r m. intensive care units the clinical pharmacist role to ...
 
The Effects of Nurse Staffing on Adverse Events, Morbidity, Mortality, and Me...
The Effects of Nurse Staffing on Adverse Events, Morbidity, Mortality, and Me...The Effects of Nurse Staffing on Adverse Events, Morbidity, Mortality, and Me...
The Effects of Nurse Staffing on Adverse Events, Morbidity, Mortality, and Me...
 
A SYSTEMATIC REVIEW ON SELF-REPORTED QUESTIONNAIRES TO ASSESS MEDICATION ADH...
 A SYSTEMATIC REVIEW ON SELF-REPORTED QUESTIONNAIRES TO ASSESS MEDICATION ADH... A SYSTEMATIC REVIEW ON SELF-REPORTED QUESTIONNAIRES TO ASSESS MEDICATION ADH...
A SYSTEMATIC REVIEW ON SELF-REPORTED QUESTIONNAIRES TO ASSESS MEDICATION ADH...
 
Recruitment Metrics from TogetherRA: A Study in Rheumatoid Arthritis Patients...
Recruitment Metrics from TogetherRA: A Study in Rheumatoid Arthritis Patients...Recruitment Metrics from TogetherRA: A Study in Rheumatoid Arthritis Patients...
Recruitment Metrics from TogetherRA: A Study in Rheumatoid Arthritis Patients...
 
Final copy
Final copyFinal copy
Final copy
 
med surg falls poster
med surg falls postermed surg falls poster
med surg falls poster
 
Measurement of outcomes in epidemiology
Measurement of outcomes in epidemiologyMeasurement of outcomes in epidemiology
Measurement of outcomes in epidemiology
 
group 6 Poster 409
group 6 Poster 409group 6 Poster 409
group 6 Poster 409
 
Costs of ADRs
Costs of ADRsCosts of ADRs
Costs of ADRs
 

Viewers also liked

1. angiokeratoma
1. angiokeratoma1. angiokeratoma
1. angiokeratoma
DrShrikant Sonune
 
Psoriasis -- female skin changes in various hormonal stages throughout life—p...
Psoriasis -- female skin changes in various hormonal stages throughout life—p...Psoriasis -- female skin changes in various hormonal stages throughout life—p...
Psoriasis -- female skin changes in various hormonal stages throughout life—p...Younis I Munshi
 
Jurnalku pompa
Jurnalku pompaJurnalku pompa
Jurnalku pompaAmardhiana
 
A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course an...
A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course an...A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course an...
A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course an...
Mutiple Sclerosis
 
Honey Protects Liver from Melamine Toxicity
Honey Protects Liver from Melamine ToxicityHoney Protects Liver from Melamine Toxicity
Honey Protects Liver from Melamine Toxicity
Bee Healthy Farms
 
Protective Effect of Egyptian Propolis Against Rabbit Pasteurellosis
Protective Effect of Egyptian Propolis Against Rabbit PasteurellosisProtective Effect of Egyptian Propolis Against Rabbit Pasteurellosis
Protective Effect of Egyptian Propolis Against Rabbit Pasteurellosis
Bee Healthy Farms
 

Viewers also liked (8)

1. angiokeratoma
1. angiokeratoma1. angiokeratoma
1. angiokeratoma
 
Pla with soyabene oil
Pla with soyabene oilPla with soyabene oil
Pla with soyabene oil
 
Psoriasis -- female skin changes in various hormonal stages throughout life—p...
Psoriasis -- female skin changes in various hormonal stages throughout life—p...Psoriasis -- female skin changes in various hormonal stages throughout life—p...
Psoriasis -- female skin changes in various hormonal stages throughout life—p...
 
Jurnalku pompa
Jurnalku pompaJurnalku pompa
Jurnalku pompa
 
A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course an...
A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course an...A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course an...
A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course an...
 
Honey Protects Liver from Melamine Toxicity
Honey Protects Liver from Melamine ToxicityHoney Protects Liver from Melamine Toxicity
Honey Protects Liver from Melamine Toxicity
 
Protective Effect of Egyptian Propolis Against Rabbit Pasteurellosis
Protective Effect of Egyptian Propolis Against Rabbit PasteurellosisProtective Effect of Egyptian Propolis Against Rabbit Pasteurellosis
Protective Effect of Egyptian Propolis Against Rabbit Pasteurellosis
 
Morphometric Analysis to Infer Hydrological Behaviour of Lidder Watershed, We...
Morphometric Analysis to Infer Hydrological Behaviour of Lidder Watershed, We...Morphometric Analysis to Infer Hydrological Behaviour of Lidder Watershed, We...
Morphometric Analysis to Infer Hydrological Behaviour of Lidder Watershed, We...
 

Similar to 628362

Running head CRITIQUE QUANTITATIVE, QUALITATIVE, OR MIXED METHODS.docx
Running head CRITIQUE QUANTITATIVE, QUALITATIVE, OR MIXED METHODS.docxRunning head CRITIQUE QUANTITATIVE, QUALITATIVE, OR MIXED METHODS.docx
Running head CRITIQUE QUANTITATIVE, QUALITATIVE, OR MIXED METHODS.docx
todd271
 
Evidence-based intrapartum practice and.pdf
Evidence-based intrapartum practice and.pdfEvidence-based intrapartum practice and.pdf
Evidence-based intrapartum practice and.pdf
heidilee52
 
humanastatinarticle
humanastatinarticlehumanastatinarticle
humanastatinarticlenewtonsapple
 
Paediatricians provide higher quality care to children and adolescents in pri...
Paediatricians provide higher quality care to children and adolescents in pri...Paediatricians provide higher quality care to children and adolescents in pri...
Paediatricians provide higher quality care to children and adolescents in pri...
Javier González de Dios
 
Research Critique Guidelines Essay Example Paper.docx
Research Critique Guidelines Essay Example Paper.docxResearch Critique Guidelines Essay Example Paper.docx
Research Critique Guidelines Essay Example Paper.docx
write22
 
Evidence based projectMSN, Walden UniversityNURS-6052CDr.
Evidence based projectMSN, Walden UniversityNURS-6052CDr. Evidence based projectMSN, Walden UniversityNURS-6052CDr.
Evidence based projectMSN, Walden UniversityNURS-6052CDr.
BetseyCalderon89
 
Case control
Case controlCase control
Case control
Babahgaru
 
Cancer Clinical Trials_ USA Scenario and Study Designs.pdf
Cancer Clinical Trials_ USA Scenario and Study Designs.pdfCancer Clinical Trials_ USA Scenario and Study Designs.pdf
Cancer Clinical Trials_ USA Scenario and Study Designs.pdf
ProRelix Research
 
New York State Drug Court Program
New York State Drug Court ProgramNew York State Drug Court Program
New York State Drug Court Program
ErikaAGoyer
 
Research methodology 101
Research methodology 101Research methodology 101
Research methodology 101Hesham Gaber
 
Research.docx
Research.docxResearch.docx
Research.docx
sheeba307290
 
508ReseaRchBritish Journal of Midwifery • July 2016 • .docx
508ReseaRchBritish Journal of Midwifery • July 2016 • .docx508ReseaRchBritish Journal of Midwifery • July 2016 • .docx
508ReseaRchBritish Journal of Midwifery • July 2016 • .docx
troutmanboris
 
Rapid Response Team Essay.docx
Rapid Response Team Essay.docxRapid Response Team Essay.docx
Rapid Response Team Essay.docx
write22
 
Contraceptive methods &amp; factors associated with modern contraceptives use
Contraceptive methods &amp; factors associated with modern contraceptives useContraceptive methods &amp; factors associated with modern contraceptives use
Contraceptive methods &amp; factors associated with modern contraceptives use
Anjum Hashmi MPH
 
Module 4 Submodule 4. 2 Final June 2007
Module 4 Submodule 4. 2 Final June 2007Module 4 Submodule 4. 2 Final June 2007
Module 4 Submodule 4. 2 Final June 2007Flavio Guzmán
 
BREAST CANCER AND SOME EPIDEMIOLOGICAL FACTORS:
BREAST CANCER AND SOME EPIDEMIOLOGICAL FACTORS:BREAST CANCER AND SOME EPIDEMIOLOGICAL FACTORS:
BREAST CANCER AND SOME EPIDEMIOLOGICAL FACTORS:
Mario Guillermo Simonovich
 
INTERGRATIVE REVIEW 14Equip.docx
INTERGRATIVE REVIEW             14Equip.docxINTERGRATIVE REVIEW             14Equip.docx
INTERGRATIVE REVIEW 14Equip.docx
vrickens
 
QuantitativeMixed-MethodsAmerican InterContinental Un.docx
QuantitativeMixed-MethodsAmerican InterContinental Un.docxQuantitativeMixed-MethodsAmerican InterContinental Un.docx
QuantitativeMixed-MethodsAmerican InterContinental Un.docx
makdul
 
Evidence-Based Practices & NursingIntroduction Normally,.docx
Evidence-Based Practices & NursingIntroduction       Normally,.docxEvidence-Based Practices & NursingIntroduction       Normally,.docx
Evidence-Based Practices & NursingIntroduction Normally,.docx
SANSKAR20
 

Similar to 628362 (20)

Running head CRITIQUE QUANTITATIVE, QUALITATIVE, OR MIXED METHODS.docx
Running head CRITIQUE QUANTITATIVE, QUALITATIVE, OR MIXED METHODS.docxRunning head CRITIQUE QUANTITATIVE, QUALITATIVE, OR MIXED METHODS.docx
Running head CRITIQUE QUANTITATIVE, QUALITATIVE, OR MIXED METHODS.docx
 
Evidence-based intrapartum practice and.pdf
Evidence-based intrapartum practice and.pdfEvidence-based intrapartum practice and.pdf
Evidence-based intrapartum practice and.pdf
 
humanastatinarticle
humanastatinarticlehumanastatinarticle
humanastatinarticle
 
Paediatricians provide higher quality care to children and adolescents in pri...
Paediatricians provide higher quality care to children and adolescents in pri...Paediatricians provide higher quality care to children and adolescents in pri...
Paediatricians provide higher quality care to children and adolescents in pri...
 
Research Critique Guidelines Essay Example Paper.docx
Research Critique Guidelines Essay Example Paper.docxResearch Critique Guidelines Essay Example Paper.docx
Research Critique Guidelines Essay Example Paper.docx
 
Evidence based projectMSN, Walden UniversityNURS-6052CDr.
Evidence based projectMSN, Walden UniversityNURS-6052CDr. Evidence based projectMSN, Walden UniversityNURS-6052CDr.
Evidence based projectMSN, Walden UniversityNURS-6052CDr.
 
Case control
Case controlCase control
Case control
 
Cancer Clinical Trials_ USA Scenario and Study Designs.pdf
Cancer Clinical Trials_ USA Scenario and Study Designs.pdfCancer Clinical Trials_ USA Scenario and Study Designs.pdf
Cancer Clinical Trials_ USA Scenario and Study Designs.pdf
 
New York State Drug Court Program
New York State Drug Court ProgramNew York State Drug Court Program
New York State Drug Court Program
 
Research methodology 101
Research methodology 101Research methodology 101
Research methodology 101
 
Research.docx
Research.docxResearch.docx
Research.docx
 
508ReseaRchBritish Journal of Midwifery • July 2016 • .docx
508ReseaRchBritish Journal of Midwifery • July 2016 • .docx508ReseaRchBritish Journal of Midwifery • July 2016 • .docx
508ReseaRchBritish Journal of Midwifery • July 2016 • .docx
 
Rapid Response Team Essay.docx
Rapid Response Team Essay.docxRapid Response Team Essay.docx
Rapid Response Team Essay.docx
 
Contraceptive methods &amp; factors associated with modern contraceptives use
Contraceptive methods &amp; factors associated with modern contraceptives useContraceptive methods &amp; factors associated with modern contraceptives use
Contraceptive methods &amp; factors associated with modern contraceptives use
 
Module 4 Submodule 4. 2 Final June 2007
Module 4 Submodule 4. 2 Final June 2007Module 4 Submodule 4. 2 Final June 2007
Module 4 Submodule 4. 2 Final June 2007
 
BREAST CANCER AND SOME EPIDEMIOLOGICAL FACTORS:
BREAST CANCER AND SOME EPIDEMIOLOGICAL FACTORS:BREAST CANCER AND SOME EPIDEMIOLOGICAL FACTORS:
BREAST CANCER AND SOME EPIDEMIOLOGICAL FACTORS:
 
INTERGRATIVE REVIEW 14Equip.docx
INTERGRATIVE REVIEW             14Equip.docxINTERGRATIVE REVIEW             14Equip.docx
INTERGRATIVE REVIEW 14Equip.docx
 
CONTROL Surveillance Paper
CONTROL Surveillance PaperCONTROL Surveillance Paper
CONTROL Surveillance Paper
 
QuantitativeMixed-MethodsAmerican InterContinental Un.docx
QuantitativeMixed-MethodsAmerican InterContinental Un.docxQuantitativeMixed-MethodsAmerican InterContinental Un.docx
QuantitativeMixed-MethodsAmerican InterContinental Un.docx
 
Evidence-Based Practices & NursingIntroduction Normally,.docx
Evidence-Based Practices & NursingIntroduction       Normally,.docxEvidence-Based Practices & NursingIntroduction       Normally,.docx
Evidence-Based Practices & NursingIntroduction Normally,.docx
 

More from Jonny Luna

9789584476180.04
9789584476180.049789584476180.04
9789584476180.04Jonny Luna
 
Riu008001 0028
Riu008001 0028Riu008001 0028
Riu008001 0028Jonny Luna
 
00006250 201409000-00021
00006250 201409000-0002100006250 201409000-00021
00006250 201409000-00021Jonny Luna
 
Optimal evaluation of_the_infertile_female(1)
Optimal evaluation of_the_infertile_female(1)Optimal evaluation of_the_infertile_female(1)
Optimal evaluation of_the_infertile_female(1)Jonny Luna
 
guidelines summary
guidelines summaryguidelines summary
guidelines summary
Jonny Luna
 
Anatomía de tórax
Anatomía de tóraxAnatomía de tórax
Anatomía de tórax
Jonny Luna
 
Anatomia del dorso
Anatomia del dorsoAnatomia del dorso
Anatomia del dorsoJonny Luna
 

More from Jonny Luna (13)

C059553
C059553C059553
C059553
 
Mecanismo
MecanismoMecanismo
Mecanismo
 
Guias15
Guias15Guias15
Guias15
 
A03v56n1
A03v56n1A03v56n1
A03v56n1
 
9789584476180.04
9789584476180.049789584476180.04
9789584476180.04
 
Riu008001 0028
Riu008001 0028Riu008001 0028
Riu008001 0028
 
00006250 201409000-00021
00006250 201409000-0002100006250 201409000-00021
00006250 201409000-00021
 
Optimal evaluation of_the_infertile_female(1)
Optimal evaluation of_the_infertile_female(1)Optimal evaluation of_the_infertile_female(1)
Optimal evaluation of_the_infertile_female(1)
 
7 1
7 17 1
7 1
 
Nihms204875
Nihms204875Nihms204875
Nihms204875
 
guidelines summary
guidelines summaryguidelines summary
guidelines summary
 
Anatomía de tórax
Anatomía de tóraxAnatomía de tórax
Anatomía de tórax
 
Anatomia del dorso
Anatomia del dorsoAnatomia del dorso
Anatomia del dorso
 

Recently uploaded

Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...
Oleg Kshivets
 
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?Report Back from SGO 2024: What’s the Latest in Cervical Cancer?
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?
bkling
 
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...
VarunMahajani
 
Couples presenting to the infertility clinic- Do they really have infertility...
Couples presenting to the infertility clinic- Do they really have infertility...Couples presenting to the infertility clinic- Do they really have infertility...
Couples presenting to the infertility clinic- Do they really have infertility...
Sujoy Dasgupta
 
Maxilla, Mandible & Hyoid Bone & Clinical Correlations by Dr. RIG.pptx
Maxilla, Mandible & Hyoid Bone & Clinical Correlations by Dr. RIG.pptxMaxilla, Mandible & Hyoid Bone & Clinical Correlations by Dr. RIG.pptx
Maxilla, Mandible & Hyoid Bone & Clinical Correlations by Dr. RIG.pptx
Dr. Rabia Inam Gandapore
 
Flu Vaccine Alert in Bangalore Karnataka
Flu Vaccine Alert in Bangalore KarnatakaFlu Vaccine Alert in Bangalore Karnataka
Flu Vaccine Alert in Bangalore Karnataka
addon Scans
 
ANATOMY AND PHYSIOLOGY OF URINARY SYSTEM.pptx
ANATOMY AND PHYSIOLOGY OF URINARY SYSTEM.pptxANATOMY AND PHYSIOLOGY OF URINARY SYSTEM.pptx
ANATOMY AND PHYSIOLOGY OF URINARY SYSTEM.pptx
Swetaba Besh
 
Charaka Samhita Sutra sthana Chapter 15 Upakalpaniyaadhyaya
Charaka Samhita Sutra sthana Chapter 15 UpakalpaniyaadhyayaCharaka Samhita Sutra sthana Chapter 15 Upakalpaniyaadhyaya
Charaka Samhita Sutra sthana Chapter 15 Upakalpaniyaadhyaya
Dr KHALID B.M
 
ARTHROLOGY PPT NCISM SYLLABUS AYURVEDA STUDENTS
ARTHROLOGY PPT NCISM SYLLABUS AYURVEDA STUDENTSARTHROLOGY PPT NCISM SYLLABUS AYURVEDA STUDENTS
ARTHROLOGY PPT NCISM SYLLABUS AYURVEDA STUDENTS
Dr. Vinay Pareek
 
KDIGO 2024 guidelines for diabetologists
KDIGO 2024 guidelines for diabetologistsKDIGO 2024 guidelines for diabetologists
KDIGO 2024 guidelines for diabetologists
د.محمود نجيب
 
micro teaching on communication m.sc nursing.pdf
micro teaching on communication m.sc nursing.pdfmicro teaching on communication m.sc nursing.pdf
micro teaching on communication m.sc nursing.pdf
Anurag Sharma
 
MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdf
MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdfMANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdf
MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdf
Jim Jacob Roy
 
Non-respiratory Functions of the Lungs.pdf
Non-respiratory Functions of the Lungs.pdfNon-respiratory Functions of the Lungs.pdf
Non-respiratory Functions of the Lungs.pdf
MedicoseAcademics
 
Physiology of Chemical Sensation of smell.pdf
Physiology of Chemical Sensation of smell.pdfPhysiology of Chemical Sensation of smell.pdf
Physiology of Chemical Sensation of smell.pdf
MedicoseAcademics
 
Factory Supply Best Quality Pmk Oil CAS 28578–16–7 PMK Powder in Stock
Factory Supply Best Quality Pmk Oil CAS 28578–16–7 PMK Powder in StockFactory Supply Best Quality Pmk Oil CAS 28578–16–7 PMK Powder in Stock
Factory Supply Best Quality Pmk Oil CAS 28578–16–7 PMK Powder in Stock
rebeccabio
 
Charaka Samhita Sutra Sthana 9 Chapter khuddakachatuspadadhyaya
Charaka Samhita Sutra Sthana 9 Chapter khuddakachatuspadadhyayaCharaka Samhita Sutra Sthana 9 Chapter khuddakachatuspadadhyaya
Charaka Samhita Sutra Sthana 9 Chapter khuddakachatuspadadhyaya
Dr KHALID B.M
 
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journey
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness JourneyTom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journey
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journey
greendigital
 
Are There Any Natural Remedies To Treat Syphilis.pdf
Are There Any Natural Remedies To Treat Syphilis.pdfAre There Any Natural Remedies To Treat Syphilis.pdf
Are There Any Natural Remedies To Treat Syphilis.pdf
Little Cross Family Clinic
 
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...
kevinkariuki227
 
BENIGN PROSTATIC HYPERPLASIA.BPH. BPHpdf
BENIGN PROSTATIC HYPERPLASIA.BPH. BPHpdfBENIGN PROSTATIC HYPERPLASIA.BPH. BPHpdf
BENIGN PROSTATIC HYPERPLASIA.BPH. BPHpdf
DR SETH JOTHAM
 

Recently uploaded (20)

Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...
 
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?Report Back from SGO 2024: What’s the Latest in Cervical Cancer?
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?
 
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...
 
Couples presenting to the infertility clinic- Do they really have infertility...
Couples presenting to the infertility clinic- Do they really have infertility...Couples presenting to the infertility clinic- Do they really have infertility...
Couples presenting to the infertility clinic- Do they really have infertility...
 
Maxilla, Mandible & Hyoid Bone & Clinical Correlations by Dr. RIG.pptx
Maxilla, Mandible & Hyoid Bone & Clinical Correlations by Dr. RIG.pptxMaxilla, Mandible & Hyoid Bone & Clinical Correlations by Dr. RIG.pptx
Maxilla, Mandible & Hyoid Bone & Clinical Correlations by Dr. RIG.pptx
 
Flu Vaccine Alert in Bangalore Karnataka
Flu Vaccine Alert in Bangalore KarnatakaFlu Vaccine Alert in Bangalore Karnataka
Flu Vaccine Alert in Bangalore Karnataka
 
ANATOMY AND PHYSIOLOGY OF URINARY SYSTEM.pptx
ANATOMY AND PHYSIOLOGY OF URINARY SYSTEM.pptxANATOMY AND PHYSIOLOGY OF URINARY SYSTEM.pptx
ANATOMY AND PHYSIOLOGY OF URINARY SYSTEM.pptx
 
Charaka Samhita Sutra sthana Chapter 15 Upakalpaniyaadhyaya
Charaka Samhita Sutra sthana Chapter 15 UpakalpaniyaadhyayaCharaka Samhita Sutra sthana Chapter 15 Upakalpaniyaadhyaya
Charaka Samhita Sutra sthana Chapter 15 Upakalpaniyaadhyaya
 
ARTHROLOGY PPT NCISM SYLLABUS AYURVEDA STUDENTS
ARTHROLOGY PPT NCISM SYLLABUS AYURVEDA STUDENTSARTHROLOGY PPT NCISM SYLLABUS AYURVEDA STUDENTS
ARTHROLOGY PPT NCISM SYLLABUS AYURVEDA STUDENTS
 
KDIGO 2024 guidelines for diabetologists
KDIGO 2024 guidelines for diabetologistsKDIGO 2024 guidelines for diabetologists
KDIGO 2024 guidelines for diabetologists
 
micro teaching on communication m.sc nursing.pdf
micro teaching on communication m.sc nursing.pdfmicro teaching on communication m.sc nursing.pdf
micro teaching on communication m.sc nursing.pdf
 
MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdf
MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdfMANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdf
MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdf
 
Non-respiratory Functions of the Lungs.pdf
Non-respiratory Functions of the Lungs.pdfNon-respiratory Functions of the Lungs.pdf
Non-respiratory Functions of the Lungs.pdf
 
Physiology of Chemical Sensation of smell.pdf
Physiology of Chemical Sensation of smell.pdfPhysiology of Chemical Sensation of smell.pdf
Physiology of Chemical Sensation of smell.pdf
 
Factory Supply Best Quality Pmk Oil CAS 28578–16–7 PMK Powder in Stock
Factory Supply Best Quality Pmk Oil CAS 28578–16–7 PMK Powder in StockFactory Supply Best Quality Pmk Oil CAS 28578–16–7 PMK Powder in Stock
Factory Supply Best Quality Pmk Oil CAS 28578–16–7 PMK Powder in Stock
 
Charaka Samhita Sutra Sthana 9 Chapter khuddakachatuspadadhyaya
Charaka Samhita Sutra Sthana 9 Chapter khuddakachatuspadadhyayaCharaka Samhita Sutra Sthana 9 Chapter khuddakachatuspadadhyaya
Charaka Samhita Sutra Sthana 9 Chapter khuddakachatuspadadhyaya
 
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journey
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness JourneyTom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journey
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journey
 
Are There Any Natural Remedies To Treat Syphilis.pdf
Are There Any Natural Remedies To Treat Syphilis.pdfAre There Any Natural Remedies To Treat Syphilis.pdf
Are There Any Natural Remedies To Treat Syphilis.pdf
 
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...
 
BENIGN PROSTATIC HYPERPLASIA.BPH. BPHpdf
BENIGN PROSTATIC HYPERPLASIA.BPH. BPHpdfBENIGN PROSTATIC HYPERPLASIA.BPH. BPHpdf
BENIGN PROSTATIC HYPERPLASIA.BPH. BPHpdf
 

628362

  • 1. Hindawi Publishing Corporation Infectious Diseases in Obstetrics and Gynecology Volume 2012, Article ID 628362, 9 pages doi:10.1155/2012/628362 Research Article A First Look at ChorioamnionitisManagement Practice Variation among US Obstetricians Mara B. Greenberg,1 Britta L. Anderson,2 Jay Schulkin,2 Mary E. Norton,1 and Natali Aziz1 1Division of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, Lucile Packard Children’s Hospital at Stanford, Stanford University, 300 Pasteur Drive HH333, Stanford, CA 94305, USA 2Department of Research, American College of Obstetricians and Gynecologists, P.O. Box 70620, Washington, WA 20024, USA Correspondence should be addressed toMara B. Greenberg, mbgreenberg@yahoo.com Received 21 August 2012; Accepted 26 November 2012 Academic Editor: Catalin S. Buhimschi Copyright © 2012 Mara B. Greenberg et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Objective. To examine practice patterns for diagnosis and treatment of chorioamnionitis among US obstetricians. Study Design.We distributed a mail-based survey to members of the American College of Obstetricians and Gynecologists, querying demographics, practice setting, and chorioamnionitis management strategies. We performed univariable and multivariable analyses. Results. Of 500 surveys distributed, 53.8% were returned, and 212 met study criteria and were analyzed. Most respondents work in group practice (66.0%), perform >100 deliveries per year (60.0%), have been in practice >10 years (77.3%), and work in a nonuniversity setting (85.1%). Temperature plus one additional criterion (61.3%) was the most common diagnostic strategy. Over 25 different primary antibiotic regimens were reported, including use of a single agent by 30.0% of respondents. A wide range of postpartum antibiotic duration was reported from no postpartum treatment (34.5% after vaginal delivery, 11.3% after cesarean delivery) to 48 hours of postpartum treatment (24.7% after vaginal delivery, 32.1% after cesarean delivery). No practitioner characteristic was independently associated with diagnostic or therapeutic strategies in multivariable analysis. Conclusion. There is a wide variation in contemporary clinical practices for the management of chorioamnionitis. This may represent a dearth of level I evidence. Future prospective clinical trials may provide more evidence-based practice recommendations for diagnosis and treatment of chorioamnionitis. 1. Introduction Chorioamnionitis, infection of the amniotic fluid, mem-branes, placenta, and/or decidua, is a common intrapartum complication, affecting up to 10% of women during labor in the USA [1–6]. Potentially serious adverse maternal sequelae of chorioamnionitis include increased risk of operative delivery, postpartum hemorrhage, and postdelivery infection [1, 6–8]. Neonatal risks include sepsis and potential long-term consequences such as cerebral palsy [6–12]. The patho-genesis of chorioamnionitis is thought to be polymicrobial and involves bacteria that colonize the vagina including Gram-negative organisms and anaerobes. When chorioam-nionitis is suspected based on clinical findings prior to delivery, administration of broad spectrum antibiotics has been shown to be effective in reducing maternal and fetal morbidity and mortality [1–6, 9]. Which diagnostic and therapeutic strategies are associ-ated with optimalmaternal and neonatal outcomes is unclear due to a dearth of prospective randomized trials comparing various management strategies [1–6, 13]. Clinical chorioam-nionitis is traditionally diagnosed based on elevatedmaternal temperature associated with additional findings including maternal tachycardia, fetal tachycardia, maternal leuko-cytosis, uterine tenderness, and purulent amniotic fluid [1–6]. Number and type of diagnostic criteria associated with least maternal and neonatal morbidity have not been evaluated in a systematic fashion.Much of the peer-reviewed literature on chorioamnionitis either lacks a description of formal diagnostic criteria or reports utilization of elevated
  • 2. 2 Infectious Diseases in Obstetrics and Gynecology temperature plus two additional criteria [1–5, 8]. With regard to evidence-based treatment, though randomized and observational trials have demonstrated a reduction in neonatal sepsis with intrapartum rather than postpartum treatment for chorioamnionitis, there have been few head to head comparisons of different intrapartum regimens [14–17]. In contrast, several studies have demonstrated similar efficacy among different durations of postpartum therapy, with regard to resolution of maternal infection and development of postoperative infectious complications [18– 21]. Likely due to limitations in the breadth of available data, guidelines are lacking regarding necessary clinical and laboratory diagnostic criteria, optimal antibiotic regimens, and duration of therapy. As a result of this uncertainty, practice patterns are likely to vary, potentially significantly. We hypothesized that obstetric care providers have a wide variety of practice patterns with regard to management of intrapartum chorioamnionitis. Identification of such variations in practice would allow us to target areas in which future investigation could be useful. In addition, for those aspects of chorioamnionitis management for which high quality data are available, it would be useful to define areas in which enhanced provider education regarding best practices might be beneficial. The purpose of this study was to deter-mine the current practice patterns among obstetricians in the USA regarding chorioamnionitis management strategies.We also examined provider characteristics associated with the use of different diagnostic and therapeutic practices. 2.Materials andMethods Questionnaires were mailed in January 2011 to 500 Fellows and Junior Fellows of the American College of Obstetricians and Gynecologists (ACOG). The potential participants were members of the Collaborative Ambulatory ResearchNetwork (CARN), a consortium established to facilitate assessment of clinical practice patterns. CARN is comprised of 1200 practicing obstetrician gynecologists who have volunteered to participate in 3–5 survey studies each year. The pool of potential participants was quasi randomly selected from the total CARN membership. The entire CARN sample pool was divided into groups of 100, all of which were similar with regard to mean age, gender, and ACOG district distribution. Five groups of 100 were then randomly chosen for this study sample. Each potential participant was assigned an identification number that was used to track the respondent while maintaining anonymity. A cover letter was included with the questionnaire, orienting survey recipients to the study and indicating a response deadline of approximately 3 weeks from the mailing date. Mailings also included postage paid return envelopes with the recipient identification number. All non-respondents received a second mailing of the questionnaire 5 weeks after the first mailing. A final mailing was sent approximately 5 weeks later. Questionnaires returned by July 2011 were included in the study. The survey consisted of 27 questions including 7 demographic, 9 on practice characteristics, 6 on chorioamnionitis diagnostic practices, and 5 on treatment practices. Question formats includedmultiple choice, yes/no, and Likert response scale.We conducted a pilot survey of 157 physicians and certified nurse midwives in June 2010 and utilized the results to eliminate ambiguity and redundancy in the questionnaire content and format. A sample of the questions on diagnostic and treatment strategies is listed in Table 1. Student’s t-tests were used to compare group means of continuous variables. Differences in categorical measures were assessed using Chi-squared test. Multivariable logistic regression analyses were used to control for potential con-founders in assessing differences between groups. For the multivariable models, we utilized four predictor variables thought to be clinically important, regardless of significance in univariable analysis: region of practice, number of years in practice, practice volume, and practice setting. We analyzed data using R version 2.11.1 (2010-05-31, The R Foundation for Statistical Computing). We considered a two-sided alpha of <0.05 to be significant. Institutional review board exemption was granted at Stanford University. 3. Results and Discussion 3.1. Results. Of the 500 surveys distributed, 269 were return-ed for a 53.8% response rate. Forty were excluded due to insufficient survey completion and 17 because the respon-dents reported that they do not currently practice inpatient obstetrics. The remaining 212 completed surveys were included in the analysis. Participants represent 42 different US states, Canada (3 providers) and Bahamas (1 provider), with female and male providers equally represented and a median provider age of 51 (Table 2). The majority of providers work in private or community practice (83.2%), have been in practice greater than 10 years (77.3%), and perform over 100 deliveries per year (60.0%) (Table 2). Table 3 shows diagnostic management practices. Most providers reported using temperature plus one additional criterion for diagnosis of chorioamnionitis (61.3%), with the most common temperature threshold being 38.0 degrees Centigrade. The majority of providers use interventions to attempt to lower maternal temperature prior to making the diagnosis of chorioamnionitis (69.0%), including 7.1% who administer acetaminophen for this purpose prior to diagnosis. The presence of epidural analgesia influences the likelihood of diagnosing chorioamnionitis for 41.2% of providers, and 9.0% are influenced by their institution’s neonatal sepsis workup policy. Responses about treatment practices are shown in Table 3. Respondents listed over 25 different antibiotic reg-imens as their primary choice for treating chorioamnionitis. A regimen containing ampicillin and gentamicin is used by 65.3% of providers, while 30.0% of respondents use a single-agent regimen. A regimen without Gram-negative coverage, either ampicillin alone or cefazolin alone, is used by 14.5% of providers. A wide range of duration of postpartum antibi-otic therapy was reported from no postpartum treatment (34.5% after vaginal delivery, 11.3% after cesarean delivery)
  • 3. Infectious Diseases in Obstetrics and Gynecology 3 Table 1: Questions on diagnostic and treatment strategies. Describe your most common strategy for diagnosing intrapartum chorioamnionitis. Elevated temperature alone Elevated temperature plus at least one additional sign or symptom Elevated temperature plus at least two additional signs or symptoms At least one sign or symptom alone without elevated temperature Other: What temperature is your threshold for diagnosing intrapartum chorioamnionitis? 37.8◦C (100.0◦F) 37.9◦C (100.2◦F) 38.0◦C (100.4◦F) 38.1◦C (100.6◦F) 38.2◦C (100.8◦F) Other: What strategies do you use to lower maternal temperature before deciding whether a patient meets diagnostic criteria for chorioamnionitis? Choose all that apply. None IV fluid bolus PO hydration Tylenol or other antipyretics External cooling (application of ice or cool cloths) Other: If a patient has a fever alone, with no additional signs or symptoms of chorioamnionitis, is it likely that your decision to treat for chorioamnionitis would be influenced by whether the patient has an epidural? No Yes, I would be more likely to diagnose chorioamnionitis and treat accordingly in a patient with a fever and an epidural than one without an epidural Yes, I would be less likely to diagnose chorioamnionitis and treat accordingly in a patient with a fever and an epidural than one without an epidural Do you think your institution’s policy on neonatal sepsis workup influences how frequently you diagnose maternal chorioamnionitis? No Yes, I am more likely to diagnose maternal chorioamnionitis because of my institution’s policy on neonatal sepsis workup Yes, I am less likely to diagnose maternal chorioamnionitis because of my institution’s policy on neonatal sepsis workup What is the most common antibiotic regimen you use for treating intrapartum chorioamnionitis?∗ Ampicillin Azithromycin Ancef (Cefazolin) Cefotetan Cefoxitin Clindamycin Ertapenem Gentamicin, daily dosing Gentamicin, TID dosing Metronidazole Unasyn (Ampicillin/sulbactam) Zosyn (Piperacillin/tazobactam)
  • 4. 4 Infectious Diseases in Obstetrics and Gynecology Table 1: Continued. Ampicillin plus Gentamicin, daily dosing Ampicillin plus Gentamicin, TID dosing Ampicillin plus Gentamicin daily dosing plus Clindamycin Ampicillin plus Gentamicin TID dosing plus Clindamycin Other: What is the most common antibiotic regimen you use for treating intrapartum chorioamnionitis in the setting of cesarean delivery?∗ Same regimen as above Different regimen (please check all that apply): Ampicillin Azithromycin Ancef (Cefazolin) Cefotetan Cefoxitin Clindamycin Ertapenem Gentamicin, daily dosing Gentamicin, TID dosing Metronidazole Unasyn (Ampicillin/sulbactam) Zosyn (Piperacillin/tazobactam) Ampicillin plus Gentamicin, daily dosing Ampicillin plus Gentamicin, TID dosing Ampicillin plus Gentamicin daily dosing plus Clindamycin Ampicillin plus Gentamicin TID dosing plus Clindamycin Other: What is your strategy for postpartum treatment after a vaginal delivery, in women diagnosed with intrapartum chorioamnionitis, in the absence of endometritis? No additional antibiotics after delivery One additional dose of antibiotics after delivery Continue antibiotics for 24 hours after delivery Continue antibiotics for 48 hours after delivery Continue antibiotics for 24 hours after last fever Continue antibiotics for 48 hours after last fever Other: What is your strategy for postpartum treatment after a cesarean delivery, in women diagnosed with intrapartum chorioamnionitis, in the absence of endometritis? No additional antibiotics after delivery One additional dose of antibiotics after delivery Continue antibiotics for 24 hours after delivery Continue antibiotics for 48 hours after delivery Continue antibiotics for 24 hours after last fever Continue antibiotics for 48 hours after last fever Other:
  • 5. Infectious Diseases in Obstetrics and Gynecology 5 Table 1: Continued. Do you treat with oral antibiotics after a patient has finished her postpartum course of IV antibiotics? Yes No ∗Responses were not limited to one of the choices listed but rather one or more than one antibiotic choice as needed to accurately reflect respondents’ primary regimen. to 48 hours of postpartum treatment (24.7% after vaginal delivery, 32.1% after cesarean delivery). Sixteen percent of providers utilize oral antibiotics after completion of the intravenous regimen. We examined the relationship between management strategies and the following provider characteristics: region of practice, length of time in practice, practice setting, and practice volume. In univariable analysis, university-based practitioners were less likely to report use of single-agent regimen (13.8% versus 32.6%, P = 0.04) and more likely to report sufficient Gram-negative coverage (100% versus 83.4%, P = 0.02) when compared to non-university-based practitioners. Those in practice for 10 years were more likely to report using a regimen with sufficient Gram-negative coverage than those in practice for 10 years (97.8% versus 82.0%, P = 0.007) and less likely to prescribe a course of oral antibiotics after completion of the intravenous course (8.3% versus 24.7%, P = 0.01). Region of practice was associated with likelihood of reporting use of ≤1 dose of additional antibiotics after vaginal delivery compared with 1 dose with more providers from the Midwest treating with ≤1 antibiotic dose (67.9%) compared to providers from other regions (west 46.7%, south 36.2%, northeast 26.3%, P 0.001). No other provider characteristics were associated with differences in management strategy in univariable anal-ysis (data not shown). In multivariable logistic regression analysis controlling for the practice volume, region, setting, and length of time in practice, no provider characteristics were independently statistically significantly associated with differences in any chorioamnionitis management strategy. 3.2. Discussion. We demonstrate a wide variation in prac-tice patterns for management of chorioamnionitis among obstetric care providers in the USA.We identified significant heterogeneity in essentially all aspects of management, including criteria for diagnosis, influences on likelihood of making the diagnosis, choice of antibiotics, and type and duration of postpartum treatment. This wide variety of diagnostic and treatment strategies is likely in part due to a dearth of high-quality clinical data to guide practice and indicates a need for further investigation into optimal strategies for the management of chorioamnionitis. For example, 60% of obstetricians require elevated temperature plus one additional criterion when making the diagnosis of chorioamnionitis, and a quarter of clinicians use elevated temperature alone. The latter strategy likely results in more patients being diagnosed with and treated for intrapartum infection than strategies that require additional signs or symptoms. Whether or not this lower threshold for diagnosis of chorioamnionitis is associated with fewer adverse outcomes is unclear and deserves further study. Over two-thirds of providers utilize strategies to attempt to lower maternal temperature prior to making a diagnosis of chorioamnionitis. This may represent uncertainty by obstetricians regarding whether treatment in the setting of elevated temperature alone is associated with optimal outcomes, as well as acknowledgement that there are a variety of influences on maternal temperature in labor [1– 6, 22–27]. As with other diagnostic criteria, there are no data regarding maternal or neonatal outcomes associated with initial management of maternal fever using intravenous fluids, acetaminophen, and/or external cooling prior to diagnosing chorioamnionitis and initiating antibiotics in labor. Sixty percent of providers do not consider the presence of epidural analgesia in the diagnosis of chorioamnionitis, while the remainder are influenced by presence of epidural in making diagnostic and treatment decisions. This hetero-geneity of management styles reflects the lack of consensus on best practices regarding the complex relationship between epidural, maternal fever, and neonatal outcomes, despite multiple publications addressing this issue [22–27]. While current literature suggests that elevated maternal temper-ature associated with epidural use is not associated with neonatal sepsis, a consensus regarding how presence of epidural should inform chorioamnionitis diagnostic thresh-old has yet to be reached [22–27]. The vast majority of obstetricians surveyed do not take their institution’s neonatal sepsis workup policy into account when diagnosing chorioamnionitis. However, of the 7% of providers who are influenced by such policies, more than two-thirds report that they are less likely to diagnose and treat clinically suspected chorioamnionitis as a result of their institution’s policy. Presumably this indicates a degree of uncertainty regarding the cost-benefit ratio of exposing neonates to invasive procedures, given the lack of an evident number needed to treat to prevent neonatal harm when the clinical diagnosis of chorioamnionitis is uncertain. A 2002 Cochrane Database Review indicated that there are insufficient data on which to base a recommendation for optimal antibiotic regimens in the setting of chorioam-nionitis [13]. Not surprisingly, our results demonstrate a wide variety of antibiotic regimens in common use. Most of these regimens contain sufficient Gram-negative coverage and consist of broad spectrumantibiotics that cover for beta-lactamase producing aerobes and anaerobes, as has been recommended by expert consensus and nonrandomized published studies [1–6, 9, 13–16, 22–27]. However, 15%
  • 6. 6 Infectious Diseases in Obstetrics and Gynecology Table 2: Respondent characteristics. Respondent characteristics N = 212 Female 103 (48.8%) Male 109 (51.2%) Median age (IQR) 51 (43–60) Physician ethnicity Non-HispanicWhite 173 (82.0%) Other 38 (18.0%) Number of deliveries annually 100 84 (40.0%) 100 126 (60.0%) Region of USa West 46 (22.0%) Midwest 54 (25.8%) South 69 (33.0%) Northeast 38 (18.2%) Practice location Suburban 106 (50.2%) Urban 75 (35.5%) Rural 25 (11.8%) Other 5 (2.5%) Predominant patient insurance type Private 154 (73.3%) Public 55 (26.2%) Uninsured 1 (0.5%) Predominant patient ethnicity Non-HispanicWhite 148 (70.8%) HispanicWhite 32 (15.3%) Other 29 (13.9%) Years in practice 0–5 5 (2.4%) 6–10 43 (20.3%) 11–15 43 (20.3%) 16–20 25 (11.8%) 21–25 34 (16.0%) 26–30 27 (12.7%) 30 35 (16.5%) Practice setting Private or community 174 (83.2%) University or academic 29 (13.9%) Government 5 (2.4%) Other 1 (0.5%) Practice type Obgyn partnership/group 140 (66.0%) University/teaching institution 26 (12.3%) Solo practice 38 (17.9%) Laborist/hospitalist 0 Other 8 (3.8%) aLocation of practice divided into four regions for purposes of analysis, according to the Centers for Disease Control and Prevention “Geographic Regions of the United States,” http://www.cdc.gov/. of providers use ampicillin or cefazolin alone, regimens that do not contain Gram-negative coverage and are theoret-ically insufficient for covering the spectrum of microbes commonly seen with chorioamnionitis. We found that use of a regimen with insufficient Gram-negative coverage is associated with practice type and duration, with community physicians and those in practice for 10 years more likely to use such a regimen than those in university practice and more recently in training. While use of a single agent appears to be common practice (30% of respondents), no studies have compared the use of a single agent to a multidrug regimen for treatment of chorioamnionitis. Use of a single agent is also associated with practice type, with fewer physicians in university practice reporting use of a single agent as compared to those in community practice. These discrepancies may be indicative of variation in management styles between university and community practices. Several studies have investigated the association between duration of postpartum therapy, resolution of maternal infection, and development of postoperative infectious complications [18–21]. While randomized trials have not demonstrated a difference in efficacy between “traditional” 24–48 hour postpartum courses and “abbreviated” courses consisting of ≤1 postpartum dose of antibiotics, the majority of providers continue to use 24–48 hour courses. Unlike other practice patterns studied, region of practice but not practice type is associated with likelihood of adopting an abbreviated postpartum antibiotic course.Whilemost obste-tricians do not use oral antibiotic therapy after completion of an intravenous postpartum course, a significant minority (16%) uses oral antibiotics to complete a longer treatment course. This practice is in contrast with randomized data demonstrating lack of benefit of such a strategy [28]. While this study describes clear differences in the management of chorioamnionitis amongst a diverse group of obstetric providers, it is not without limitations. These include a relatively small sample size, which may decrease our ability to detect potential differences in management practices attributable to variability in provider character-istics. Similarly, our findings may not be generalizable to practitioners outside of the ACOG membership and the demographic included. The response rate of 54% may have led to nonresponse bias, though this is near the upper end of the 35%–60% response rate typical of previous ACOG surveys [29, 30]. Additionally among those surveyed, a wide variety of practice settings and geographic regions were represented. Due to the constraints of a postal-based survey strategy, we were also limited in our ability to capture more comprehensive details about chorioamnionitis management strategies and their associated outcomes or about the risk profiles of respondent’s patient populations. Many providers likely have a more nuanced approach to the diagnosis and treatment of chorioamnionitis than can be appreciated based on the brief closed-ended survey approach employed. 4. Conclusions This study is the first to report on chorioamnionitis man-agement patterns among US obstetricians. The heterogeneity of practice patterns we demonstrate has several potential implications. Many aspects of variation in management
  • 7. Infectious Diseases in Obstetrics and Gynecology 7 Table 3: Diagnostic and treatment strategies. Diagnostic strategies N = 212 Diagnosis based on Temperature alone 56 (26.4%) Temperature plus one additional criterion 130 (61.3%) Temperature plus two additional criteria 16 (7.6%) Other 10 (4.7%) Most common temperature threshold (degrees Centigrade) 37.9 6 (2.8%) 38.0 154 (73.0%) 38.1 23 (10.9%) 38.2 18 (8.5%) Other 10 (4.7%) Strategies used to lower temperature prior to diagnosis None 65 (31.0%) Intravenous fluids 124 (59.0%) Acetaminophen 15 (7.1%) Other 6 (2.9%) Influenced by presence of epidural in making diagnosis No 124 (58.8%) More likely to diagnose 10 (4.7%) Less likely to diagnose 77 (36.5%) Neonatal sepsis workup required for all chorioamnionitis diagnoses Yes 170 (83.3%) No 34 (16.7%) Influenced by neonatal sepsis workup policy in making diagnosis No 191 (91.0%) More likely to diagnose 5 (2.3%) Less likely to diagnose 14 (6.7%) Treatment Strategies N = 212 Primary treatment regimen Ampicillin and gentamicin ± additional agent 135 (65.2%) Single agent 62 (30.0%) Includes Gram-negative coverage 177 (85.5%) Does not include Gram-negative coverage 30 (14.5%) Change regimens for cesarean delivery Yes 99 (46.9%) No 112 (53.1%) Postpartum treatment strategy after vaginal delivery No additional antibiotics 73 (34.6%) 1 additional dose 20 (9.5%) 24 hours postpartum 56 (26.5%) 24 hours afebrile 3 (1.4%) 48 hours postpartum 52 (24.7%) 48 hours afebrile 4 (1.9%) Other 3 (1.4%) Postpartum treatment strategy after cesarean delivery No additional antibiotics 24 (11.3%) 1 additional dose 15 (7.1%) 24 hours postpartum 70 (33.0%)
  • 8. 8 Infectious Diseases in Obstetrics and Gynecology Table 3: Continued. 24 hours afebrile 17 (8.0%) 48 hours postpartum 68 (32.1%) 48 hours afebrile 16 (7.6%) Other 2 (0.9%) Treat with oral antibiotics after intravenous course completed Yes 34 (16.2%) No 176 (83.8%) strategy may reasonably be thought to represent lack of high-quality data necessary to guide practice in a coherent fashion. These understudied aspects of care include number and type of diagnostic criteria, influence of epidural on diagnosis, and type of antibiotic regimen. While some heterogeneity in practice may be acceptable, such as in the use of numerous antibiotics that cover the same bacteria but have varying prices, availability, ease of use, and tolerability, studies deter-mining optimal maternal and neonatal outcomes associated with particular management strategies in these understudied areas may be helpful to inform best practices. Data regarding which strategies are associated with decreased rates of neonatal sepsis and improvements in long-term child health are important to guide providers in these areas as these are associated with the most current uncertainty.With regard to several management issues that have already been studied in randomized trials, such as duration and type of postpartum therapy, our results indicate that efforts should be made to increase dissemination of best practice guidelines across obstetric demographics. Acknowledgments This study was funded in part by Grant no UA6MC19010, through the Maternal and Child Health Research Programs, Health Resources and Services Adminstration, U.S. Depart-ment of Health and Human Services, presented at the Society forMaternal FetalMedicine 32nd AnnualMeeting, February 6–11, 2012, Dallas, TX. References [1] A. T. N. Tita andW.W. Andrews, “Diagnosis andmanagement of clinical chorioamnionitis,” Clinics in Perinatology, vol. 37, no. 2, pp. 339–354, 2010. [2] L. C. Gilstrap III and S. M. Cox, “Acute chorioamnionitis,” Obstetrics and Gynecology Clinics of North America, vol. 16, no. 2, pp. 373–379, 1989. [3] D. E. Soper, C. G. Mayhall, andH. P.Dalton, “Risk factors for intraamniotic infection: a prospective epidemiologic study,” American Journal of Obstetrics and Gynecology, vol. 161, no. 3, pp. 562–566, 1989. [4] E. R. Newton, “Chorioamnionitis and intraamniotic infec-tion,” Clinical Obstetrics and Gynecology, vol. 36, no. 4, pp. 795–808, 1993. [5] J. W. Riggs and J. D. Blanco, “Pathophysiology, diagnosis, and management of intraamniotic infection,” Seminars in Perinatology, vol. 22, no. 4, pp. 251–259, 1998. [6] R. K. Edwards, “Chorioamnionitis and labor,” Obstetrics and Gynecology Clinics of North America, vol. 32, no. 2, pp. 287– 296, 2005. [7] J. C. Hauth, L. C. Gilstrap, G. D. V. Hankins, and K. D. Connor, “Term maternal and neonatal complications of acute chorioamnionitis,” Obstetrics and Gynecology, vol. 66, no. 1, pp. 59–62, 1985. [8] D. J. Rouse, M. Landon, K. J. Leveno et al., “The maternal-fetal medicine units cesarean registry: chorioamnionitis at term and its duration—relationship to outcomes,” American Journal of Obstetrics and Gynecology, vol. 191, no. 1, pp. 211– 216, 2004. [9] R. S. Gibbs and P. Duff, “Progress in pathogenesis and man-agement of clinical intraamniotic infection,” American Journal of Obstetrics and Gynecology, vol. 164, no. 5 I, pp. 1317–1326, 1991. [10] J. M. Alexander, D. M.McIntire, and K. J. Leveno, “Chorioam-nionitis and the prognosis for term infants,” Obstetrics and Gynecology, vol. 94, no. 2, pp. 274–278, 1999. [11] J. G. Shatrov, S. C. M. Birch, L. T. Lam, J. A. Quinlivan, S. McIntyre, and G. L. Mendz, “Chorioamnionitis and cerebral palsy: ameta-analysis,” Obstetrics and Gynecology, vol. 116, no. 2, pp. 387–392, 2010. [12] N. Aziz, Y.W. Cheng, and A. B. Caughey, “Neonatal outcomes in the setting of preterm premature rupture of membranes complicated by chorioamnionitis,” Journal of Maternal-Fetal and Neonatal Medicine, vol. 22, no. 9, pp. 780–784, 2009. [13] L. Hopkins and F. Smaill, “Antibiotic regimens for man-agement of intraamniotic infection,” Cochrane Database of Systematic Reviews, no. 3, Article ID CD003254, 2002. [14] R. S. Sperling, R. S. Ramamurthy, andR. S. Gibbs, “A compari-son of intrapartum versus immediate postpartum treatment of intra-amniotic infection,” Obstetrics and Gynecology, vol. 70, no. 6, pp. 861–865, 1987. [15] R. S. Gibbs, M. J. Dinsmoor, E. R. Newton, and R. S. Ramamurthy, “A randomized trial of intrapartum versus immediate postpartum treatment of women with intra-amniotic infection,” Obstetrics and Gynecology, vol. 72, no. 6, pp. 823–828, 1988. [16] L. C. Gilstrap, K. J. Leveno, S. M. Cox, J. S. Burris, M. Mashburn, and C. R. Rosenfeld, “Intrapartum treatment of acute chorioamnionitis: impact on neonatal sepsis,” American Journal of Obstetrics and Gynecology, vol. 159, no. 3, pp. 579– 583, 1988. [17] M. C. Maberry and L. C. Gilstrap, “Intrapartum antibiotic therapy for suspected intraamniotic infection: impact on the fetus and neonate,” Clinical Obstetrics and Gynecology, vol. 34, no. 2, pp. 345–351, 1991. [18] S. J. Chapman and J. Owen, “Randomized trial of single-dose versus multiple-dose cefotetan for the postpartum treatment of intrapartum chorioamnionitis,” American Journal of Obstet-rics and Gynecology, vol. 177, no. 4, pp. 831–834, 1997.
  • 9. Infectious Diseases in Obstetrics and Gynecology 9 [19] R. K. Edwards and P. Duff, “Single additional dose postpartum therapy for women with chorioamnionitis,” Obstetrics and Gynecology, vol. 102, no. 5, pp. 957–961, 2003. [20] M. A. Turnquest, H. Y. How, C. R. Cook et al., “Chorioam-nionitis: is continuation of antibiotic therapy necessary after cesarean section?” American Journal of Obstetrics and Gynecol-ogy, vol. 179, no. 5, pp. 1261–1266, 1998. [21] C. Berry, K. A. Hansen, and J. F. McCaul, “Abbreviated antibi-otic therapy for clinical chorioamnionitis: a randomized trial,” Journal of Maternal-Fetal Medicine, vol. 3, no. 5, pp. 216–218, 1994. [22] B. L. Leighton and S.H.Halpern, “The effects of epidural anal-gesia on labor, maternal, and neonatal outcomes: a systematic review,” American Journal of Obstetrics and Gynecology, vol. 186, no. 5, pp. S69–S77, 2002. [23] L. Goetzl, A. Cohen, F. Frigoletto Jr., J. M. Lang, and E. Lieberman, “Maternal epidural analgesia and rates ofmaternal antibiotic treatment in a low-risk nulliparous population,” Journal of Perinatology, vol. 23, no. 6, pp. 457–461, 2003. [24] O. Apantaku and V. Mulik, “Maternal intra-partum fever,” Journal of Obstetrics and Gynaecology, vol. 27, no. 1, pp. 12– 15, 2007. [25] L. E. Riley, A. C. Celi, A. B.Onderdonk et al. et al., “Association of epidural-related fever and noninfectious inflammation in termlabor,” Obstetrics and Gynecology, vol. 117, no. 3, pp. 588– 595, 2011. [26] E. Lieberman, J. M. Lang, F. Frigoletto Jr., D. K. Richardson, S. A. Ringer, and A. Cohen, “Epidural analgesia, intrapartum fever, and neonatal sepsis evaluation,” Pediatrics, vol. 99, no. 3, pp. 415–419, 1997. [27] F. A. de Orange, R. Passini Jr., M. M. Amorim, T. Almeida, and A. Barros, “Combined spinal and epidural anaesthesia and maternal intrapartum temperature during vaginal delivery: a randomized clinical trial,” British Journal of Anaesthesia, vol. 107, no. 5, pp. 762–768, 2011. [28] M. J. Dinsmoor, E. R. Newton, and R. S. Gibbs, “A random-ized, double-blind, placebo-controlled trial of oral antibiotic therapy following intravenous antibiotic therapy for postpar-tum endometritis,” Obstetrics and Gynecology, vol. 77, no. 1, pp. 60–62, 1991. [29] D. M. Kissin, M. L. Power, E. B. Kahn et al., “Attitudes and practices of obstetrician-gynecologists regarding influenza vaccination in pregnancy,” Obstetrics and Gynecology, vol. 118, no. 5, pp. 1074–1080, 2011. [30] K. A. Matteson, B. L. Anderson, S. B. Pinto, V. Lopes, J. Schulkin, and M. A. Clark, “Practice patterns and attitudes about treating abnormal uterine bleeding: a national survey of obstetricians and gynecologists,” American Journal of Obstet-rics and Gynecology, vol. 205, no. 4, pp. 321.e1–321.e8, 2011.
  • 10. MEDIATORS of INFLAMMATION Journal of Gastroenterology Research and Practice Submit your manuscripts at http://www.hindawi.com Stem Cells International Hindawi Publishing Corporation http://www.hindawi.com Volume 2014 Hindawi Publishing Corporation http://www.hindawi.com Volume 2014 Behavioural Neurology Hindawi Publishing Corporation http://www.hindawi.com Volume 2014 Disease Markers Hindawi Publishing Corporation http://www.hindawi.com Volume 2014 International Journal of Endocrinology Hindawi Publishing Corporation http://www.hindawi.com Volume 2014 BioMed Research International Hindawi Publishing Corporation http://www.hindawi.com Volume 2014 Journal of Oncology Hindawi Publishing Corporation http://www.hindawi.com Volume 2014 Oxidative Medicine and Cellular Longevity Hindawi Publishing Corporation http://www.hindawi.com Volume 2014 The Scientific World Journal Hindawi Publishing Corporation http://www.hindawi.com Volume 2014 Journal of Immunology Research Hindawi Publishing Corporation http://www.hindawi.com Volume 2014 PPAR Research Hindawi Publishing Corporation http://www.hindawi.com Volume 2014 Journal of Obesity Hindawi Publishing Corporation http://www.hindawi.com Volume 2014 Journal of Ophthalmology Hindawi Publishing Corporation http://www.hindawi.com Volume 2014 Computational and Mathematical Methods in Medicine Hindawi Publishing Corporation http://www.hindawi.com Volume 2014 Diabetes Research Hindawi Publishing Corporation http://www.hindawi.com Volume 2014 AIDS Research and Treatment Hindawi Publishing Corporation http://www.hindawi.com Volume 2014 Hindawi Publishing Corporation http://www.hindawi.com Volume 2014 Evidence-Based Complementary and Alternative Medicine Hindawi Publishing Corporation http://www.hindawi.com Parkinson’s Disease Volume 2014 Hindawi Publishing Corporation http://www.hindawi.com Volume 2014