This document discusses community acquired pneumonia (CAP). It begins by defining CAP and discussing its epidemiology and classification. It then covers the incidence, clinical presentation, radiological manifestations, and typical microbiological findings of CAP. It discusses specific investigations and pathogens involved in severe CAP. Scoring systems for assessing CAP severity, including PSI, CURB-65 and CRB-65, are outlined. Guidelines are provided on treatment based on severity, including empiric antibiotic choice. Risk factors for drug-resistant pathogens and tuberculosis are noted. The document concludes with recommendations for empiric treatment of severe CAP patients admitted to the ICU.
Pneumonia - Community Acquired Pneumonia (CAP)Arshia Nozari
An overview to Community Acquired Pneumonia; It's Pathophysiology, Etiology, Epidemiology, Diagnosis and Treatment according to Harrison's Internal Medicine, 20th Edition (2018).
Pneumonia - Community Acquired Pneumonia (CAP)Arshia Nozari
An overview to Community Acquired Pneumonia; It's Pathophysiology, Etiology, Epidemiology, Diagnosis and Treatment according to Harrison's Internal Medicine, 20th Edition (2018).
This is a paper presentation held by Dr. Yiannis Verginadis at the 1st International Workshop on Cloud Security and Data Privacy by Design (CloudSPD'15) in Limassol, Cyprus.
Pneumonia lecture,Describe the common pathogenesis and pathogens of pneumonia
Discuss diagnosis and initial management of community acquired pneumonia (CAP)
Understand features of the Pneumonia PORT Severity Index
Discuss the IDSA/ATS guidelines and recommendations for final antibiotic choice
Understand issues in basic management for pneumonia in children, nursing home patients, and immunocompromised patients.
respiratory inspections are common in elderly people and often times,that tickles into the lungs.More often than not they have comorbiidites,like Diabetes,hypertension etc.Hence,the treatment has to be different and some times the prognosis is guarded
Clinical management guidelines for swine flu at civic centre on 5 feb2015Vinod Nikhra
A lecture by Dr Vinod Nikhra at Conference on Swine Flu, organised by Health Department, South Delhi Municipal Corporation at Civic Centre, Delhi on 05 February 2015.
Sepsis biomarkers an update by Dr Puneet JainPuneet Jain
sepsis biomarkers play a crucial role in decision making and management of sepsis cases. these biomarkers can be diagnostic, prognostic or theranostic. CRP and Procalcitonin are most widely used and studied biomarkers.
Definition of sepsis and septic shock.
The new definition of sepsis 2016 conference.
SIRS, SOFA, QSOFA
Most common pathogen causing sepsis.
Pathogenesis and pathophysiology of sepsis
Biomarkers for detection of sepsis and septic shock
Preseason, sCD14 Subtype marker
Comparison of Procalcitonin and CRP with presepsin.
Mechanism of presepsin detection.
Management of sepsis.
psychological aspects of Bronchial asthma.Hiba Ashibany
this lecture ( psychological aspects of bronchial asthma) has been presented by Dr. Heba ashebani/ Abusetta chest center, in the event of Global asthma day 2018.
this lecture( Allergic bronchopulmonary aspergillosis), has been presented by Dr.Anas azarmouh / azreig horpital. , that was in the event of Global asthma day 2018.
3. Which of the following symptoms is
not bad prognostic factor for CAP?
1-fever
2-Pleuretic chest pain
3-Altered mental status
4-Dyspnea
4. Which of the following clinical findings is
not poor prognostic factor in CAP?
1-low temperature < 35 C
2-High temperature >40 C
3-Systolic BP < 100 mmHg
3-Pulse >125 bpm
5-RR > 30 bpm
5. Which of the following lab. Results is
not risk factor for severe CAP?
1-Na < 130 mmol/L
2-Glucose =/> 250 mg%
3-PaO2 < 60 mmHg
4-CRP >150 mg/L
5-Hct < 30%
6. When you suspect about 60-70% of patients will have
complete resolving of pneumonia radiologically?
1-1 week .
2-2 weeks.
4-3 weeks
4-4 weeks
5-6 weeks
7. Which drug should not be used for treatment
of sCAP due Pseudomonas aeruginosa?
1-Piperacillin-tazobactam
2- Ertapenem
3-Cefepime
4-Imipenem/cilastatin
5-meropenem
11. Health care associated pneumonia
HCAP is defined as pneumonia that occurs in non-
hospitalized patient with extensive healthcare contact,
as defined by one or more of the following :
●Intravenous therapy, wound care, or intravenous
chemotherapy within the prior 30 days
●Residence in a nursing home or other long-term care
facility
●Hospitalization in an acute care hospital for two or more
days within the prior 90 days
●Attendance at hospital or hemodialysis clinic within the
prior 30 days
23. Microbiological investigations in patients with CAP
All patients
• Sputum: direct smear by Gram stain
and Ziehl–Neelsen stain.
Culture and sensitivity testing
• Blood culture: frequently positive
in pneumococc pneumonia
• Serology: acute and convalescent titers for:
-Mycoplasma, -
Chlamydia, -
Legionella, -
viral infections. -
Pneumococcal Ag detection in serum or urine
• PCR: Mycoplasma can be detected from swab of
oropharynx
Gram stain of sputum showing Gram-positive
diplococci characteristic of Strep. pneumoniae (arrows).
Mycobacterium tuberculosis (stained red) in sputum
24. Severe community-acquired pneumonia “sCAP”
The previous tests plus consider:
• Tracheal aspirate (TBAS), induced sputum, BAL , protected
brush specimen (PBS) or percutaneous needle aspiration
(PCNA).
.Direct fluorescent antibody
stain for Legionella and viruses
• Serology:
.Legionella Ag in urine.
.Pneumococcal Ag in sputum and blood.
.Immediate IgM for Mycoplasma
• Cold agglutinins: positive in 50% of patients with
Mycoplasma
Sputum direct fluorescent antibody stain showing Legionella infection.
25. Selected patients
• Throat/nasopharyngeal swabs: helpful in
children or during influenza epidemic
• Pleural fluid: should always be sampled when
present in more than trivial amounts, preferably with
ultrasound (US) guidance
35. Multivariable analyses
Different variables in different patients
-Demographic
-Different comorbidities
-Different in physical examinations
-Different in lab and radiological findings
42. Point total
Risk
R
i
s
k
c
l
a
s
s
Recommended site of
care
No predictors Low I Outpatient
≤ 70 Low II Outpatient
71 to 90 Low II
I
Inpatient (briefly)
91 to 130 Moderate I
V
Inpatient
> 130 High V Inpatient
(3)-A prediction rule to identify low-risk patients with CPA
Pneumonia Severity Index limitation
44. For all these reasons look for other
practical scoring system for
assessment of patient severity
45.
46. Confusion
Urea > 7 mmol/l
Respiratory Rate: ≥ 30 /minute
Blood pressure: 90/60 mmHg
65 years
IS THERE A SIMPLER WAY?
CURB-65
47. Questionnaire
Mental Test Score (10 points)
The following questions are put to the patient. Each question
correctly answered scores 1 point. A score of 7-8 or less suggests
cognitive impairment at the time of testing, although further and
more formal tests are necessary to confirm a diagnosis of dementia,
delirium or other causes of cognitive impairment.
References
(1)-Hodkinson, HM (1972). "Evaluation of a mental test score for assessment of mental impairment in the elderly."
Confusion:
Defined as a Mental
Test Score of 8 or less,
or new disorientation
in person, place or
time. (A urea of
7 mmol/L ≅ 20 mg/dL.)
48. Hospital CURB-65. *Defined as a Mental Test Score of 8 or less, or new disorientation in person,
place or time. (A urea of 7 mmol/L ≅ 20 mg/dL.)
Severity scoring of CAP according to CURB-65
52. Confusion
Respiratory rate ≥ 30/min
Blood pressure (SBP≤ 90 or DBP≤60)
Age ≥ 65
0 1 or 2 3 or 4
Low Risk
mortality 1.2%
Intermediate Risk
mortality 8.13%
High Risk
mortality 31%
Severity scoring of CAP according to CRB-65
Likely suitable for
home treatment
Consider
hospital referral
Urgent hospital
admission
60. Hospital CURB-65. *Defined as a Mental Test Score of 8 or less, or new disorientation in person,
place or time. (A urea of 7 mmol/L ≅ 20 mg/dL.)
Treatment plain according to -CURB-65
61. Confusion
Respiratory rate ≥ 30/min
Blood pressure (SBP≤ 90 or DBP≤60)
Age ≥ 65
0 1 or 2 3 or 4
Low Risk
mortality 1.2%
Intermediate Risk
mortality 8.13%
High Risk
mortality 31%
Treatment plain according to CRB-65
Likely suitable for
home treatment
Consider
hospital referral
Urgent hospital
admission
62. Indications for referral to ITU
• CURB-65 score 4–5 or CRB-65 score 3-4
failing to respond rapidly to initial
management
• Persisting hypoxia (PaO2 < 8 kPa (60 mmHg))
despite high concentrations of oxygen
• Progressive hypercapnia
• Severe acidosis
• Circulatory shock
• Reduced conscious level
67. Factors increasing the risk of TB
:Patient-related
• Age (children > young adults < elderly)
• First-generation immigrants from high-prevalence
countries
• Close contacts of patients with smear-positive
pulmonary TB
• Overcrowding (prisons, collective dormitories);
homelessness (doss houses and hostels)
• Chest radiographic evidence of self-healed TB
• Primary infection < 1 year previously
• Smoking: cigarettes .
68. Factors increasing the risk of TB
Associated diseases:
• Immunosuppression: HIV, anti-TNF therapy, high-dose
corticosteroids, cytotoxic agents
• Malignancy (especially lymphoma and leukaemia)
• Type 1 diabetes mellitus
• Chronic renal failure
• Silicosis
• Gastrointestinal disease associated with malnutrition
(gastrectomy, jejuno-ileal bypass, cancer of the
pancreas, malabsorption)
• Deficiency of vitamin D or A
• Recent measles: increases risk of child contracting TB
74. Risk factors for drug-resistant S. pneumoniae
Risk factors for drug-resistant S. pneumoniae in adults include:
●Age >65 years
●Beta-lactam, macrolide, or fluoroquinolone therapy within the past
3 to 6 months
●Alcoholism
●Medical comorbidities
●Immunosuppressive illness or therapy
●Exposure to a child in a daycare center
Recent therapy or a repeated course of therapy with beta-lactams,
macrolides, or fluoroquinolones are risk factors for pneumococcal
resistance to the same class of antibiotic . Thus, an antimicrobial agent
from an alternative class is preferred for a patient who has recently
received one of these agents
79. - ertapenem
750
severe
In patients without risk factors for or microbiologic evidence of Pseudomonas aeruginosa or MRSA
7-14
7-14
7-14
7-14
7-14
7-14
7-14
7-14
with
80. Recommendation for empiric initial antimicrobial
treatment in patients with sCAP-admitted to ICU
●In patients with risk factors for or microbiologic
evidence of Pseudomonas aeruginosa or MRSA
and Legionella spp .
81. Recommendation for empiric initial antimicrobial
treatment in patients with sCAP-admitted to ICU
●In patients with risk factors for or microbiologic
evidence of Pseudomonas aeruginosa
82.
83.
84.
85. Risk factors for P. aerginosa
The ATS emphasizes certain modifying factors that
increase the risk of infection with drug-resistant and
unusual
Risk factors for enteric gram-negative organisms are as
follows:
-recent antibiotic therapy,
-underlying cardiopulmonary disease,
-residence in a nursing home, and
-multiple medical comorbidities. Risk
factors for P aeruginosa are as follows:
-structural lung disease such as bronchiectasis,
-broad-spectrum antibiotic therapy that lasted
for at least 7 days in the past month, -
corticosteroid therapy with at least 10 mg of
prednisone per day, and -
malnutrition
90. For penicillin-allergic patients
For penicillin-allergic patients, the type and severity
of reaction should be assessed. The great majority of
patients who are allergic to penicillin by skin testing can
still receive cephalosporins (especially third-generation
cephalosporins) or carbapenems.
Skin testing is indicated in some situations. For penicillin-
allergic patients, if skin test is positive or if there is
significant concern to warrant avoidance of
cephalosporin or carbapenem, options include:
-aztreonam (2 g IV every six to eight hours) plus
levofloxacin (750 mg daily) or -
aztreonam plus moxifloxacin plus an aminoglycoside.
91. -The fluoroquinolones may be administered orally when
the patient is able to take oral medications.
-The dose of levofloxacin is the same when given
intravenously and orally, while the dose of ciprofloxacin is
750 mg orally twice daily.
92. Recommendation for empiric initial antimicrobial
treatment in patients with sCAP-admitted to ICU
●In patients with risk factors for or microbiologic
evidence of MRSA
93. Staphylococcus aureus
-Associated with debilitating illness and
often preceded by influenza. -
Radiographic features include multilobar
shadowing, cavitation, pneumatocoeles
and abscesses. -
Dissemination to other organs may cause
osteomyelitis, endocarditis or brain
abscesses. -
Mortality up to 30%
94. Cavities –Thin wall contain air only
Diagnostic criteria:
-Thin wall
-Air only
-Location of the lesion:
.On the surface of the lung1-Paraseptal
emphysema
.In side parenchyma of the lung - Pneumatocele
e.g. staph. infection
1-Paraseptal emphysema
2-Pneumatocele
95. Pneumatocele
Pneumatocele :
-Localized air collection , usually
with staph. pneumonia , but may
occur with other types of
pneumonias .
-Extension of inflammatory
exudate into the lesion may cause
formation of air-fluid level .
-More common than true lung
abscess
96. MRSA risk factors
Community associated MRSA — You can pick up MRSA outside the
hospital, especially if you:
●Have skin trauma (eg, "turf burns," cuts, or sores)
●Are an athlete
●Shave or wax to remove body hair, particularly of the armpits and groin
●Have tattoos or body piercing
●Have physical contact with a person who has draining cut or sore or is
carrier of MRSA
●Share personal items or equipment that is not cleaned or laundered
between users (such as towels or protective sport pads)
Community-associated MRSA infections may occur more commonly in
certain populations, such as daycare centers, prisons, in the military, or
in athletes who play on team. Spread of MRSA within households is
common.
97. Methicillin-resistant Staphylococcus aureus
(MRSA)
Methicillin-resistant Staphylococcus aureus (MRSA)
• Vancomycin 15 mg/kg IV q12h for 7-14d
or
• Linezolid 600mg IV or PO q12h for 7-14d
or
• Telavancin 10mg/kg IV once daily for 7-21d
(reserved for use when alternative treatments
are not suitable)
98. Recommendation for empiric initial antimicrobial
treatment in patients with sCAP-admitted to ICU
●In patients with risk factors for or microbiologic
evidence of Legionella spp .
99. Legionella pneumophila
-Middle to old age.
-Local epidemics around contaminated source, e.g.
cooling systems in hotels, hospitals.
-Person-to-person spread unusual. Some features
more common, e.g. headache, confusion, malaise,
myalgia, high fever and vomiting and diarrhoea. -
Laboratory abnormalities include hyponatraemia,
elevated liver enzymes, hypoalbuminaemia and
elevated creatine kinase. -
Risk factors: Smoking, corticosteroids, diabetes,
chronic kidney disease increase risk
100. Legionella pneumophila
• Legionella pneumophila
• Levofloxacin 750 mg IV q24h, then 750
mg/day PO for 7-14d
or
• Moxifloxacin 400 mg IV or PO q24h for 7-14d
or
• Azithromycin 500 mg IV q24h for 7-10d
102. New antimicrobials in CAP
• Tigecycline was approved by the FDA in 2009 for
adults with CAP caused by:
-S pneumoniae (penicillin-susceptible isolates),
including cases with concurrent bacteremia,
-H influenza (beta-lactamase-negative isolates),
-Legionella pneumophila.
• In a study conducted to evaluate the efficacy of
tigecycline versus levofloxacin in hospitalized
patients with CAP, tigecycline achieved cure rates
similar to those of levofloxacin in hospitalized
patients with CAP.
For patients with risk factors, tigecycline provided generally
favorable clinical outcomes.
103. New antimicrobials in CAP
• Although Tigecycline is indicated for CAP, data
from clinical trials suggest a high incidence of
adverse events, particularly gastrointestinal
adverse effects >10% (nausea , vomiting ,
diarrhea), which may limit its use.
• Dose in CAP:
• Tigecycline 100 mg IV loading dose, then 50
mg IV q12h for 7-14 d
104. New antimicrobials in CAP
• Ceftaroline fosamil is a parenteral cephalosporin
antibacterial that was approved by the FDA in 2010 for
the treatment of adults with CAP caused by:
-S pneumoniae, including cases with concurrent
bacteremia;
-S aureus (methicillin-susceptible isolates only);
-H influenza;
-K pneumonia; Klebsiella oxytoca;
-E coli.
• Ceftaroline, the active form of ceftaroline fosamil, has
broad-spectrum in vitro activity against common
causative gram-positive and gram-negative bacteria,
including MRSA.
However, there are no clinical data supporting the use of
ceftaroline fosamil for MRSA pneumonia.
105. New antimicrobials in CAP
• Ceftaroline fosamil is included in Joint Commission pneumonia
core measures as one of the recommended beta-lactam
antibiotics for CAP in immunocompetent, non-ICU patients.
• Dose:
• Ceftaroline for CAP
600 mg IV q12h; infuse over 1 h for 5-7 days
• Side effects : The most common adverse reactions occurring in
> 2% of patients :
-Diarrhea
-Nausea
-Rash
107. The β-lactam family of antibiotics
Ceftriaxone 3rdTicarcillin
Ceftazidime 3rdMezlocillin
Cefotaxime 3rdCarbenicillin
ErtapenemCefmetazoleCefuroxime 2ndAmpicillin
MeropenemCefotetanCefamandole 2ndMethicillin
AztreonamImipenemCefoxitinCephalothin 1stBenzyl-
penicillin
MonobactamsCarbapenemsCephamycinsCephalosporinsPenicillins
Cefepime 4th
108. Ertapenem
• Ertapenem is effective against Gram-negative
and Gram-positive bacteria.
It is not active against MRSA, ampicillin-resistant
enterococci, Pseudomonas aeruginosa, or
Acinetobacter species. Ertapenem has useful
activity against anaerobic bacteria.
• Note: staph. (MRSA) and Enterococcus spp. are
resistant to ertapenem.
109. Ertapenem
• Ertapenem is marketed by Merck as a first-line treatment for
community-acquired infections.
• Note: It should not be used as empirical treatment for hospital-
acquired infections (HAP) because of its lack of activity against
Pseudomonas aeruginosa.
• In practice, it is reserved primarily for use against Extended
spectrum beta-lactamase (ESBL)-producing and high level
AmpC-type beta lactamase producing Gram- negative bacteria
(e.g. Klebsilla , and E. coli).
110. Ertapenem
Dosage
• Ertapenem is dosed as:
1 g given by intravenous injection over 30
minutes, or 1 g diluted with 3.2 ml of 1%
lidocaine given intramuscularly.
• There is no oral preparation of ertapenem
available.
• Ertapenem cannot be mixed with glucose.
111. Ertapenem
• Side-effects
• There are a few adverse effects of ertapenem like
confusion and headache, which may worsen to
convulsions and seizures.
The only absolute contra-indication is a previous
anaphylactic reaction to ertapenem or other β-lactam
antibiotic.
There are no studies done in pregnant women, so the
manufacturers cannot comment on its safety in
pregnancy.
Ertapenem is not recommended for children under 3
months of age and children with meningitis.
• Clostridium difficile colitis has been associated with its
use.
112. Prevention
• More people die from pneumococcal infections (an estimated 40,000
annually in the United States) than from any other vaccine preventable
disease.
• PPV23 is recommended for:
(1)- all adults ≥65 years of age,
(2)-all patients with asplenia , and
(3)- in younger patients <64 years of age with a number of conditions that
increase the risk of invasive pneumococcal disease
-Adults who have been diagnosed with invasive pneumococcal
disease should also be vaccinated because infection with one
serotype does not necessarily provide protection against other
serotypes. And that’s why IDSA states that patients can be given pneumococcal
vaccine immediately after an episode of pneumonia.
• A single revaccination is recommended in:
(1)-adults ≥65 years of age if they were vaccinated more than 5 years
previously at a time when they were <65 years of age, and
(2)-in immunocompromised patients five years or more after the first
dose.
114. Conclusions
-CAP is a common disease in community.
-Diagnosis is made by chest x ray and signs and symptoms
of pulmonary infection.
-Follow up be observed best by CRP.
-Severity is assessed by CRB-65 score and ATS criteria.
-Antibiotic therapy lower mortality
-Antibiotic is tailored according to risk factors and
aetiologies.
-Don’t use Ertapenem for treatment of pneumonia due to
MRSA, Pseudomonas aeruginosa, or Acinetobacter species.
-Most risk factors for pseud. aerug. Infection are enteral
tube feeding and chronic respiratory diseases.
115. Conclusions
-Using a guidelines, we can simplify the treatment regimens.
-For outpatients, monotherapy with either a β-lactam, a macrolide
antibiotic, doxycycline, or a fluoroquinolone antibiotic should be
sufficient.
-For patients requiring admission to a GMF or with the absence of risk
factors for DRSP or infection with enteric gram-negative organisms, the
recommended treatment is with a combination of a β-lactam plus a
macrolide or monotherapy with a fluoroquinolone antibiotic.
-For severely ill patients with CAP (eg, patients requiring admission to
the ICU or having risk factors for P aeruginosa infection), treatment
should always be with a combination of at least two drugs and the
drugs should be appropriately selected for the suspected organism.
Examples include a β-lactam plus a macrolide antibiotic, a β-lactam
plus a fluoroquinolone antibiotic, and a β-lactam plus an
aminoglycoside plus a macrolide antibiotic.
GMW=general medical floor
119. For penicillin-allergic patients
For penicillin-allergic patients, the type and severity of reaction
should be assessed. The great majority of patients who are allergic to
penicillin by skin testing can still receive cephalosporins (especially
third-generation cephalosporins) or carbapenems.
If there is a history of mild reaction to penicillin (not an IgE-mediated
reaction, Stevens Johnson syndrome, or toxic epidermal necrolysis),
it is reasonable to administer a cephalosporin or carbapenem using
simple graded challenge (eg, give 1/10 of dose, observe closely for one
hour, then give remaining 9/10 of dose, observe closely for one hour).
Skin testing is indicated in some situations. For penicillin-allergic
patients, if skin test is positive or if there is significant concern to
warrant avoidance of cephalosporin or carbapenem, options include:
-aztreonam (2 g IV every six to eight hours) plus levofloxacin (750 mg daily)
or -aztreonam plus
moxifloxacin plus an aminoglycoside.
122. Factors increasing the risk of TB
:Patient-related
• Age (children > young adults < elderly)
• First-generation immigrants from high-prevalence
countries
• Close contacts of patients with smear-positive
pulmonary TB
• Overcrowding (prisons, collective dormitories);
homelessness (doss houses and hostels)
• Chest radiographic evidence of self-healed TB
• Primary infection < 1 year previously
• Smoking: cigarettes and bidis (Indian cigarettes made of
tobacco wrapped in temburini leaves)
123. MRSA diagnosis:
-People with skin infections can be tested for
MRSA with a culture. Results of the test are
usually available in 48 to 72 hours.
-People with infections of the lung, bone, joint,
or other internal areas usually require blood
tests as well as imaging studies (eg, x-ray, CT
scan, echocardiogram).
124. New antimicrobials in CAP
• Ceftaroline fosamil is included in Joint Commission pneumonia
core measures as one of the recommended beta-lactam
antibiotics for CAP in immunocompetent, non-ICU patients.
• Dose:
• Ceftaroline for CAP
600 mg IV q12h; infuse over 1 h for 5-7 days
• Side effects
The most common adverse reactions occurring in > 2% of
patients receiving ceftaroline :
• Diarrhea
• Nausea
• Rash
Dose adjustment in Renal Impairment
-CrCl 31-50 mL/min: 400 mg IV q12h
-CrCl 15-30 mL/min: 300 mg IV q12h
-ESRD (including hemodialysis): 200 mg IV q12h
125. Ertapenem
• Ertapenem is effective against Gram-negative and Gram-
positive bacteria.
It is not active against MRSA, ampicillin-resistant enterococci,
Pseudomonas aeruginosa, or Acinetobacter species.
Ertapenem has useful activity against anaerobic bacteria.
Ertapenem is active against most isolates of the following
micro-organisms :
-Aerobic and facultative gram-positive microorganisms:
• Note: staph. (MRSA) and Enterococcus spp. are resistant to
ertapenem.
-Aerobic and facultative gram-negative microorganisms:
.E. coli, Haemophilus influenzae (Beta-lactamase-negative
isolates only), Klebsiella pneumoniae,Moraxella catarrhalis,
Proteus mirabilis,
126. Ertapenem
-Anaerobic microorganisms:
• Ertapenem is marketed by Merck as a first-line treatment for
community-acquired infections.
• Note: It should not be used as empirical treatment for hospital-
acquired infections (HAP) because of its lack of activity against
Pseudomonas aeruginosa.
In practice, it is reserved primarily for use against Extended
spectrum beta-lactamase (ESBL)-producing and high level AmpC-
type beta lactamase producing Gram- negative bacteria (e.g.
Klebsilla , and E. coli).
127. Ertapenem
• Side-effects
• There are a few adverse effects of ertapenem like
confusion and headache, which may worsen to
convulsions and seizures.
The only absolute contra-indication is a previous
anaphylactic reaction to ertapenem or other β-lactam
antibiotic.
There are no studies done in pregnant women, so the
manufacturers cannot comment on its safety in
pregnancy. In 2006, Ertapenem became approved for
pediatric use in certain infections. Ertapenem is not
recommended for children under 3 months of age and
children with meningitis.
• Clostridium difficile colitis has been associated with its
use.
128. Mild CAP with risk factors
• Cigarette smoking
• Upper respiratory tract infections
• Alcohol
• Corticosteroid therapy
• Old age
• Recent influenza infection
• Pre-existing lung disease
• HIV
• Indoor air pollution
129. MRSA symptoms:
-Most people infected with community-associated
MRSA (CA-MRSA) have signs of a skin infection.
The skin may have a single raised red lump that is
tender, or carbuncle. The center of the raised area
may ooze pus.
-It is also possible to develop an infection in areas
other than the skin if the bacteria enter the
bloodstream through the skin e.g. on a heart valve,
in a bone, joint, or the lungs, or around devices
(such as an IV line, pacemaker, or replacement
joint). In these situations, symptoms may include
fever and fatigue, as well as pain or swelling in the
infected area.
130. MRSA diagnosis:
-People with skin infections can be tested for
MRSA with culture.
-People with infections of the lung, bone, joint,
or other internal areas usually require blood
tests as well as imaging studies (eg, x-ray, CT
scan, echocardiogram).
131. The ATS emphasizes certain modifying factors that increase the risk of
infection with drug-resistant and unusual pathogens.7 Risk factors for
drug-resistant Streptococcus pneumoniae (DRSP) include age greater
than 65 years, β-lactam therapy within the past 3 months,
immunosuppression (either as the result of an illness or induced by
treatment with corticosteroids), multiple medical comorbidities,
alcoholism, and exposure to a child in a day care center.7 Risk factors
for enteric gram-negative organisms are as follows: recent antibiotic
therapy, underlying cardiopulmonary disease, residence in a nursing
home, and multiple medical comorbidities.7 Risk factors for P
aeruginosa are as follows: structural lung disease such as
bronchiectasis, broad-spectrum antibiotic therapy that lasted for at
least 7 days in the past month, corticosteroid therapy with at least 10
mg of prednisone per day, and malnutrition
132. Prevention
• Prevention of CAP infection is mainly with the use of a approved vaccine,
which is about 60% effective in preventing bacteremia in
immunocompetent adults with pneumococcal infections.
• The vaccine PPV23 should be given routinely to:
-patients older > 65 years and to
-all patients with asplenia.
-The vaccine is also recommended for patients aged or < 64 years if they
have certain coexisting illnesses.
Revaccination is recommended for:
-patients older > 65 years who initially received the vaccine more > 5 years
earlier and the initial vaccine was administered at age less < 65 years.
-If the initial vaccine was given at age greater > 65 years, then repeated
vaccination is not indicated.
The IDSA states that patients can be given the pneumococcal vaccine
immediately after an episode of pneumonia , because infection with one
serotype does not necessarily provide protection against other serotypes.
134. Recommendation for empiric initial antimicrobial
treatment in patients with sCAP-admitted to ICU
Empiric therapy — Patients requiring admission to an ICU are more likely to have
risk factors for resistant pathogens, including community-associated MRSA and
Legionella spp .
●In patients without risk factors for or microbiologic evidence of
Pseudomonas aeruginosa or MRSA, use: -
intravenous combination therapy with potent anti-pneumococcal beta-lactam
.ceftriaxone 1 to 2 g daily,
.cefotaxime 1 to 2 g every eight hours, or
.ampicillin-sulbactam 1.5 to 3 g every six hours.
plus -either an advanced macrolide
(azithromycin 500 mg daily) or respiratory fluoroquinolone
(levofloxacin 750 mg daily or moxifloxacin 400 mg daily).
Although the optimal doses of the beta-lactams have not been studied adequately,
use the higher doses, at least initially, until the minimum inhibitory concentrations
(MICs) against possible isolates (eg, Streptococcus pneumoniae) are known.
135. Confusion: Defined as a Mental Test Score of 8
or less, or new disorientation in person, place
or time. (A urea of 7 mmol/L ≅ 20 mg/dL.)
CURB-65
136. Questionnaire
Mental Test Score (10 points)
The following questions are put to the patient. Each question correctly answered
scores 1 point. A score of 7-8 or less suggests cognitive impairment at the time of
testing, although further and more formal tests are necessary to confirm a diagnosis
of dementia, delirium or other causes of cognitive impairment.
References
(1)-Hodkinson, HM (1972). "Evaluation of a mental test score for assessment of mental impairment in the elderly."
Editor's Notes
ملك=Monarch
This can be used in polyclinic , in OPD
This can be used in polyclinic , in OPD
Increased risk factor to have resistant bacteria especially sterep pneumonia
Selected patient patient with febrile pneutropenia due ChemoTherapy - ertapenem
Selected patient patient with febrile pneutropenia due ChemoTherapy - ertapenem