Preterm labor is the labor that starts before the 37th completed week. In this presentation, we will discover causes, pathogenesis, diagnosis, clinical features, and management principles for preterm labor along with the most recent evidence.
Preterm labor is the labor that starts before the 37th completed week. In this presentation, we will discover causes, pathogenesis, diagnosis, clinical features, and management principles for preterm labor along with the most recent evidence.
Placenta previa (pluh-SEN-tuh PREH-vee-uh) occurs when a baby's placenta partially or totally covers the mother's cervix — the outlet for the uterus. Placenta previa can cause severe bleeding during pregnancy and delivery. Some of the possible causes and risk factors of placenta previa include: Low implantation of the fertilised egg. Abnormalities of the uterine lining, such as fibroids. Scarring of the uterine lining (endometrium)
Placenta previa (pluh-SEN-tuh PREH-vee-uh) occurs when a baby's placenta partially or totally covers the mother's cervix — the outlet for the uterus. Placenta previa can cause severe bleeding during pregnancy and delivery. If you have placenta previa, you might bleed throughout your pregnancy and during your delivery
Placenta previa (pluh-SEN-tuh PREH-vee-uh) occurs when a baby's placenta partially or totally covers the mother's cervix — the outlet for the uterus. Placenta previa can cause severe bleeding during pregnancy and delivery. Some of the possible causes and risk factors of placenta previa include: Low implantation of the fertilised egg. Abnormalities of the uterine lining, such as fibroids. Scarring of the uterine lining (endometrium)
Placenta previa (pluh-SEN-tuh PREH-vee-uh) occurs when a baby's placenta partially or totally covers the mother's cervix — the outlet for the uterus. Placenta previa can cause severe bleeding during pregnancy and delivery. If you have placenta previa, you might bleed throughout your pregnancy and during your delivery
Characterization and the Kinetics of drying at the drying oven and with micro...Open Access Research Paper
The objective of this work is to contribute to valorization de Nephelium lappaceum by the characterization of kinetics of drying of seeds of Nephelium lappaceum. The seeds were dehydrated until a constant mass respectively in a drying oven and a microwawe oven. The temperatures and the powers of drying are respectively: 50, 60 and 70°C and 140, 280 and 420 W. The results show that the curves of drying of seeds of Nephelium lappaceum do not present a phase of constant kinetics. The coefficients of diffusion vary between 2.09.10-8 to 2.98. 10-8m-2/s in the interval of 50°C at 70°C and between 4.83×10-07 at 9.04×10-07 m-8/s for the powers going of 140 W with 420 W the relation between Arrhenius and a value of energy of activation of 16.49 kJ. mol-1 expressed the effect of the temperature on effective diffusivity.
Accuracy of cervico vaginal fetal fibronectin test in predicting risk of spon...Open Access Research Paper
Preterm delivery is the leading cause of neonatal mortality. One of the best predictors to assess the risk of preterm labour (PTB) is by measuring fetal fibronectin (fFN) in cervico vaginal secretion after 26 weeks of pregnancy. The aim is to evaluate the diagnostic accuracy of qualitative cervico vaginal fFN in symptomatic women and asymptomatic high risk women during antenatal care. Prospective study which was conducted in Basrah Maternity and Child Hospital. It included 106 pregnant women at gestational age more than 26 weeks who had uterine contraction with or without pervious risk factors for PTB. Cervico vaginal fluid sampling was undertaken from all women included in the study after the age of 26 weeks of gestation and qualitative fFN assessment was done with 50ng/ml is the cut off point for positivity. As regard qualitative fFN assessment for predicting of PTB sensitivity, specificity, PPV, NPV, were 71%, 87%, 40.50%, 94% respectively in symptomatic women. While in asymptomatic women with previous high risk had 26% sensitivity, 84% specificity, 32% PPV, and 87% NPV. Qualitative assessment of fFN in cervico vaginal fluid is good predictive marker in detecting of PTB.
Adherent placenta occurs when there is a defect in the decidua basalis, Resulting in an abnormal invasion of the placenta directly into the substance of the uterus
Heterotopic pregnancy is defined by the presence of an intrauterine pregnancy and an ectopic pregnancy in any location, mostly in
the uterine tubes. It is a rare obstetric pathology. However, in recent years its incidence has increased due to assisted reproduction
treatments. His diagnosis remains a challenge. Ultrasound is the
most important tool in its diagnosis and early identification. Laparoscopy remains the definitive method of extrauterine pregnancy.
We present the case of a 39-year-old patient, with a gestation of 6
weeks by date of last menstrual period, with a diagnosis of heterotopic pregnancy, where the extrauterine pregnancy is located in
the uterine tube.
Similar to Placenta previa epidemiology, clinical features, diagnosis, morbidity and mortality up-todate (20)
Thai bam vet mo cu RMT - VOTASON 2023.pdfVõ Tá Sơn
Mục đích của bài này là xem xét dữ liệu lâm sàng hiện có về vai trò của RMT trong việc dự đoán kết cục của CSP được quản lý theo dõi hoặc thậm chí được điều trị và đánh giá khả năng ứng dụng lâm sàng của nó. Chúng tôi cung cấp bản tóm tắt cập nhật về bằng chứng lâm sàng về RMT như một dấu hiệu siêu âm khách quan và có thể đo lường được cũng như đề cập đến các dấu hiệu siêu âm khác của CSP.
Sinh thiết gai rau CVS những điều mẹ bầu nên biếtVõ Tá Sơn
Sinh thiết gai rau là gì?
Sinh thiết gai rau (CVS) là một xét nghiệm trước sinh. Nó được sử dụng để chẩn đoán một số dị tật bẩm sinh và bất thường về di truyền ở con bạn. Bất thường di truyền là những thay đổi trong bộ gen được truyền từ mẹ hoặc bố sang em bé, hoặc có thể là các bất thường mới phát sinh không di truyền từ bố mẹ. Những thay đổi di truyền này có thể gây ra các vấn đề sức khỏe cho em bé. Nhau thai là một cấu trúc trong tử cung cung cấp máu và chất dinh dưỡng từ mẹ sang thai nhi.
Gai rau là những phần nhỏ của mô bánh rau trông giống như ngón tay và chứa vật chất di truyền giống như thai thai nhi. Có thể có xét nghiệm đối với các rối loạn di truyền khác tùy thuộc vào tiền sử gia đình và sự sẵn có của phòng xét nghiệm tại thời điểm tiến hành thủ thuật.
Trong quá trình làm CVS, bác sĩ của bạn sẽ lấy một mẩu mô nhỏ từ nhau thai. Mẫu được sử dụng để kiểm tra sức khỏe của con bạn.
Bạn có thể lấy CVS sớm trong thai kỳ, từ 11 đến 14 tuần tuổi thai. CVS không được cung cấp cho tất cả phụ nữ mang thai một cách thường quy vì có tỷ lệ sảy thai nhỏ sau khi làm xét nghiệm.
CVS khác với một xét nghiệm tiền sản khác gọi là chọc ối. Chọc ối được thực hiện muộn hơn một chút trong thai kỳ, từ sau 15 tuần. Trao đổi với bác sĩ của bạn về việc thực hiện CVS, nước ối hoặc các xét nghiệm tiền sản khác.
Đặt hẹn sinh thiết gai rau với bác sĩ Võ Tá Sơn bệnh viện Vinmec Times City, Hà Nội 0978846100
Chọc ối amniocentesis những điều mẹ bầu cần biếtVõ Tá Sơn
Chọc ối được thực hiện như thế nào?
Chọc ối thường được thực hiện từ tuần thứ 15 đến tuần thứ 20 của thai kỳ, nhưng bạn có thể thực hiện muộn hơn nếu cần thiết.
Nó có thể được thực hiện sớm hơn, nhưng điều này có thể làm tăng nguy cơ biến chứng của chọc ối và thường tránh được.
Trong quá trình thực hiện, một cây kim dài, mảnh sẽ được đưa vào thành bụng của bạn, dưới hướng dẫn bởi hình ảnh siêu âm.
Kim được đưa vào túi ối bao quanh em bé của bạn và một mẫu nhỏ nước ối được lấy ra để phân tích.
Thời gian chọc ối thường mất khoảng 10 phút, mặc dù toàn bộ quá trình tư vấn có thể mất khoảng 30 phút.
Chọc ối thường được mô tả là làm cho bạn không thoải mái hơn là đau đớn.
Một số phụ nữ mô tả cảm giác đau tương tự như đau khi hành kinh hoặc cảm thấy áp lực khi rút kim ra.
Chọc ối với Bác sĩ Võ Tá Sơn bệnh viện Vinmec Hà Nội 0978846100
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
2. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate
https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previa… 2/17
PATHOGENESIS — The pathogenesis of placenta previa is unknown. One hypothesis is that the presence of
areas of suboptimally vascularized decidua in the upper uterine cavity due to previous surgery or multiple
pregnancies promotes implantation of trophoblast in, or unidirectional growth of, trophoblast toward the lower
uterine cavity [1,3,22]. Another hypothesis is that a particularly large placental surface area, as in multiple
gestation, increases the probability that the placenta will encroach upon/cover the cervical os.
PATHOPHYSIOLOGY OF BLEEDING — Placental bleeding is the major adverse sequelae of placenta previa. It
is thought to occur when uterine contractions or gradual changes in the cervix and lower uterine segment apply
shearing forces to the inelastic placental attachment site, resulting in partial detachment. Vaginal examination or
coitus can also disrupt this site and cause bleeding. Bleeding is primarily maternal blood from the intervillous
space, but fetal bleeding can occur if fetal vessels in the terminal villi are disrupted.
CLINICAL PRESENTATION AND COURSE
Asymptomatic finding on midtrimester ultrasound examination — The most common presentation of
placenta previa is as a finding on routine ultrasound examination at about 16 to 20 weeks of gestation for
assessment of gestational age, fetal anatomic survey, or prenatal diagnosis. One to 6 percent of pregnant
women are found to have sonographic evidence of a placenta previa on these examinations. (See
'Ultrasonography' below.)
Natural history — Approximately 90 percent of placenta previas identified on ultrasound examination before
20 weeks of gestation resolve before delivery [23]. Two theories have been proposed to account for this
phenomenon:
In either case, the placental edge overlying the cervix atrophies.
Predicting presence at delivery — Findings that suggest that a placenta previa will persist until delivery
include lack of resolution by the third trimester and extension over the os by more than 25 mm.
In a retrospective cohort study of 714 women with placenta previa, singleton gestation, and a liveborn infant ≥25
weeks of gestation, when the most recent ultrasound showed placenta previa at [24]:
Infertility treatment●
Previous abortion●
Previous uterine surgical procedure●
Maternal smoking●
Maternal cocaine use●
Male fetus●
Non-white race●
The lower uterine segment lengthens from 0.5 cm at 20 weeks of gestation to more than 5 cm at term [16].
This development of the lower uterine segment relocates the stationary lower edge of the placenta away
from the internal os.
●
Progressive unidirectional growth of trophoblastic tissue toward the fundus results in upward migration of the
placenta away from the cervix. This phenomenon has been termed "trophotropism."
●
3. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate
https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previa… 3/17
The more the placenta extends over the internal os, the more likely it is to persist until delivery. Although
available data are insufficient to make precise predictions, pooled data suggest that when the placenta extends
at least 14 to 15 mm but <25 mm over the cervical os at 18 to 23 weeks of gestation, then the probability of
placenta previa at delivery is about 20 percent; extension ≥25 mm is associated with a 40 to 100 percent
probability of placenta previa at delivery [25-29].
Low-lying placentas and placentas formerly called partial previa are most likely to resolve (eg, only 6 to 7 percent
of those diagnosed at 15 to 19 weeks and 39 to 63 percent of those diagnosed at 32 to 35 weeks were present
at delivery). Anterior placenta previas are more likely to resolve than posterior placenta previa [30].
Recommendations for follow-up sonography to determine resolution are discussed separately. (See "Placenta
previa: Management", section on 'Monitoring placental position'.)
Bleeding — In the second half of pregnancy, the most common symptom of placenta previa is relatively painless
vaginal bleeding, which occurs in up to 90 percent of persistent cases [31]. Ten to 20 percent of women present
with uterine contractions, pain, and bleeding, similar to the presentation of abruptio placenta [32,33]. (See
"Placental abruption: Pathophysiology, clinical features, diagnosis, and consequences".)
In approximately one-third of pregnancies with persistent previa, the initial bleeding episode occurs prior to 30
weeks of gestation; this group is more likely to require blood transfusions and is at greater risk of preterm
delivery and perinatal mortality than women whose bleeding begins later in gestation [32-35]. An additional one-
third of patients becomes symptomatic between 30 and 36 weeks, while most of the remaining patients have
their first bleed after 36 weeks [32,33]. About 10 percent of women reach term without bleeding. The number of
antepartum bleeding episodes and need for blood transfusion have been identified as independent predictors for
emergency cesarean delivery [36].
Antepartum bleeding from any cause is a risk factor for preterm labor and preterm premature rupture of
membranes. (See "Pathogenesis of spontaneous preterm birth", section on 'Decidual hemorrhage' and "Preterm
prelabor rupture of membranes", section on 'Risk factors'.)
DIAGNOSIS — The diagnosis of placenta previa is based on sonography and requires the identification of
echogenic homogeneous placental tissue over the internal cervical os.
Placenta previa should be suspected in any woman beyond 20 weeks of gestation who presents with vaginal
bleeding. For women who have not had a second- or third-trimester ultrasound examination, antepartum
bleeding should prompt sonographic determination of placental location before digital vaginal examination is
performed because palpation of the placenta can cause severe hemorrhage.
15 to 19 weeks – 20 percent were present at delivery if no prior cesarean delivery, and 41 percent if a prior
cesarean delivery
●
20 to 23 weeks – 45 percent were present at delivery if no prior cesarean delivery, and 73 percent if a prior
cesarean delivery
●
24 to 27 weeks – 56 percent were present at delivery if no prior cesarean delivery, and 84 percent if a prior
cesarean delivery
●
28 to 31 weeks – 88 to 89 percent were present at delivery whether or not there was a prior cesarean
delivery
●
32 to 35 weeks – 89 to 90 percent were present at delivery whether or not there was a prior cesarean
delivery
●
4. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate
https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previa… 4/17
Diagnostic criteria — The diagnosis of placenta previa is based on identification of placental tissue extending
over the internal cervical os on a second or third trimester imaging study (image 1), preferably transvaginal
ultrasound [37]. The distance (millimeters) that the placenta extends over the internal cervical os should be
described in the diagnostic report.
Of note, when the placental edge is <2 cm from, but not over, the internal os, the placenta is labeled "low-lying"
(image 2). The distance (millimeters) between the internal cervical os and the inferior edge of the placenta
should be described in the diagnostic report [38]. (See 'Morbidity of low-lying placenta' below.)
The historic terms "marginal" and "partial" for characterizing a placenta previa are no longer used, as they
referred to information gathered on a digital vaginal examination, which should be avoided and is not needed
given the superiority of ultrasound diagnosis.
Ultrasonography
Transabdominal — Transabdominal sonographic assessment of placental location is one of the standard
components of the basic obstetrical ultrasound examination, and thus can be considered a screening test for
placenta previa.
Screening performance — If the placenta-cervix distance is ≤2 cm on transabdominal ultrasound, we
perform transvaginal sonography to better define placental position and make the diagnosis. The overall false
positive rate of transabdominal ultrasound for diagnosis of placenta previa is up to 25 percent, and varies by
study design [39,40]. In a planned secondary analysis of a prospective cohort study of women with singleton
gestations undergoing both transabdominal and transvaginal cervical length measurement during the second
trimester anatomic survey, a transabdominal placenta-cervix distance threshold of 4.2 cm had sensitivity 93.3
percent, specificity 76.7 percent, negative predictive value 99.8 percent, and screen-positive rate 25.0 percent for
detection of previa [41]. A threshold of 2.8 cm yielded a sensitivity 86.7 percent, specificity 90.5 percent, negative
predictive value 99.6 percent, and screen-positive rate of 11.4 percent. Thus, a threshold of 2.8 cm maximizes
specificity while a threshold of 4.2 cm maximizes sensitivity.
Technique and pitfalls — Sagittal, parasagittal, and transverse sonographic views should be obtained
with the patient's bladder partially full.
Specific points that should be appreciated when performing transabdominal sonographic examination for
placenta previa include:
An over-distended bladder can compress the anterior lower uterine segment against the posterior lower
uterine segment to give the appearance of a previa (image 3). The diagnosis of placenta previa should not
be made without confirming placental position after the patient has emptied her bladder. Care should be
taken to not make the diagnosis of placenta previa when the lower uterine segment is contracting, which
commonly occurs after a woman empties her bladder, and obscures the relationship between the placental
edge and the cervical os.
●
A previa can be missed near term if the fetal head is low in the pelvis since acoustic shadowing from or
compression of placental tissue by the fetal skull may obscure the placental location. In these cases, the
cervix may be better visualized by placing the patient in Trendelenburg position and/or gently pushing the
fetal head cephalad with an abdominal hand or the transducer.
●
The sonographic diagnosis of a central placenta previa is readily made since the placenta is centered over
the cervix and placental tissue is imaged anterior and posterior to the cervix. Complete noncentral previas,
particularly when lateral, are more difficult to confirm. Transverse views at and above the internal cervical os
should facilitate an accurate diagnosis.
●
5. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate
https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previa… 5/17
Transvaginal — Transvaginal ultrasound (TVS) can be performed safely in patients with placenta previa
since the optimal position of the vaginal probe for visualization of the internal os is 2 to 3 cm away from the
cervix, and the angle between the cervix and vaginal probe is sufficient to prevent the probe from inadvertently
slipping into the cervical canal [42].
Performance — TVS generally provides a clearer image of the relationship between the edge of the
placenta and the internal cervical os than transabdominal ultrasound. Randomized trials and prospective
comparative studies have established the superior performance of TVS over transabdominal sonography for
diagnosis of placenta previa [43-45]. In one study of 100 suspected cases, sensitivity, specificity, and positive
and negative predictive values of TVS for diagnosis of placenta previa at cesarean were 87.5, 98.8, 93.3, 97.6
percent, respectively [46].
Use of color Doppler is employed in the cases of suspected morbidly adherent placentation (eg, accreta) or
umbilical cord in the lower uterine segment, to rule out a vasa previa. (See "Clinical features and diagnosis of
placenta accreta spectrum (placenta accreta, increta, and percreta)" and "Velamentous umbilical cord insertion
and vasa previa".)
Characteristics predictive of bleeding — Although the magnitude of bleeding risk may differ according to
the following characteristics, all patients with placentas over or in close proximity to the cervical os are at risk of
significant antepartum, intrapartum, and postpartum bleeding.
Characteristics that appear to be predictive of antepartum bleeding include:
Other ultrasound techniques — Translabial (transperineal) ultrasound imaging is an alternative technique
that provides excellent images of the cervix and placenta [58]. The use of three-dimensional ultrasound may also
improve accuracy [59].
Magnetic resonance imaging — Magnetic resonance imaging (MRI) is well-suited to the assessment of
placental-cervical relationships because of the differing magnetic resonance characteristics of the two tissues.
However, it is not used for diagnosis of placenta previa because of its high cost, limited availability, and the well-
established safety and accuracy of transvaginal sonography [38]. MRI is most useful for diagnosis of complicated
placenta previa, such as previa-accreta and previa-percreta [60]. (See "Clinical features and diagnosis of
placenta accreta spectrum (placenta accreta, increta, and percreta)", section on 'Magnetic resonance imaging'.)
ASSOCIATED FINDINGS
A posterior placenta previa may be more difficult to visualize than an anterior placenta previa, even on
transvaginal ultrasound.
●
Bleeding can result in formation of a hematoma under and/or proximate to the placenta, which can obscure
the relationship between the placental edge and the cervical os.
●
Extension over the internal os rather than lying proximate to it [47-50].●
Thick (>1 cm) placental edge and/or angle between the basal and chorionic plates greater than 45 degrees
[51,52].
●
Echo-free space in the placental edge over the internal os [53].●
Cervical length ≤3 cm [52,54,55].●
Decrease in cervical length in the third trimester [56,57].●
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Placenta previa-accreta — When placenta previa is diagnosed, the possibility of placenta previa-accreta (or
more) should be considered. In a prospective study including 723 women with placenta previa undergoing
cesarean delivery, the frequency of placenta accreta increased with an increasing number of cesarean deliveries
as follows [61]:
In another large series, composite maternal morbidity in women with placenta previa and zero, one, two, or three
prior cesarean deliveries was 15, 23, 59, and 83 percent, respectively, and almost all of the excess composite
maternal morbidity in women with a prior cesarean was related to complications associated with placenta
accreta, such as peripartum hysterectomy [62]. (See "Clinical features and diagnosis of placenta accreta
spectrum (placenta accreta, increta, and percreta)", section on 'Prenatal diagnosis'.)
Other associated findings
MORBIDITY AND MORTALITY
Maternal — Maternal morbidity from placenta previa is primarily related to antepartum and/or postpartum
hemorrhage [77]. In systematic reviews, 52 percent of women with placenta previa had antepartum bleeding
(95% CI 42.7 to 60.6 percent) [31] and 22 percent had postpartum hemorrhage (95% CI 15.8 to 28.7 percent)
[78]. Because of antepartum and/or postpartum bleeding, women with placenta previa are more likely to receive
blood transfusions (12 versus 0.8 percent in patients without previa in one study [65], 22 versus 1.2 percent in
another [8]). They are also more likely to undergo postpartum hysterectomy (5.3 versus 0.04 percent in one
study [8]), uterine/iliac artery ligation, or embolization of pelvic vessels. The risks of hemorrhage and postpartum
hysterectomy are particularly high for women with previa-accreta. (See "Clinical features and diagnosis of
placenta accreta spectrum (placenta accreta, increta, and percreta)", section on 'Consequences'.)
In women with severe hemorrhage, rapid, significant loss of intravascular volume can lead to hemodynamic
instability, decreased oxygen delivery, decreased tissue perfusion, cellular hypoxia, organ damage, and death. In
First cesarean birth, 3 percent●
Second cesarean birth, 11 percent●
Third cesarean births, 40 percent●
Fourth cesarean births, 61 percent●
Fifth or greater cesarean birth, 67 percent●
Malpresentation – The large volume of placenta in the lower portion of the uterine cavity predisposes the
fetus to assume a noncephalic lie [43,63-65].
●
Vasa previa and velamentous umbilical cord – Placenta previa is a risk factor for vasa previa and
velamentous umbilical cord insertion. (See "Velamentous umbilical cord insertion and vasa previa".)
●
Intrauterine growth restriction – An increased risk of intrauterine growth restriction has been reported by
multiple [8,32,66-71], but not all [34,35,66,72-74], investigators, and remains controversial. If a reduction in
fetal growth occurs, it is likely to be mild or due to confounding factors. For example, decreased placental
perfusion can lead to both fetal growth restriction and a suboptimal site of placental implantation. (See "Fetal
growth restriction: Evaluation and management".)
●
Congenital anomalies – Population-based cohort studies have reported a small increase in the overall rate
of congenital anomalies in pregnancies complicated by placenta previa, but no single anomaly or syndrome
was associated with the disorder [8,35,75,76].
●
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resource-rich countries, the maternal mortality rate associated with placenta previa is less than 1 percent [79],
but remains high in resource-poor countries where maternal anemia, lack of medical resources, and home births
are more common [65].
Severe maternal morbidity and maternal mortality can also be a consequence of amniotic fluid embolism
syndrome. Several studies have observed a strong association between placental pathology, such as placenta
previa, and amniotic fluid embolism syndrome [80-82]. (See "Amniotic fluid embolism syndrome".)
Neonatal — The principal causes of neonatal morbidity and mortality are related to preterm delivery [83]. In a
systematic review and meta-analysis of placental implantation abnormalities and risk of preterm delivery,
compared with no placenta previa, placenta previa was associated with a three- to fivefold increase in risk of
[84]:
In large studies, approximately 15 percent of patients with placenta previa delivered before 34 weeks of gestation
[69,85]. However, neonatal morbidity and mortality rates in pregnancies complicated by placenta previa have
fallen over the past few decades because of improvements in obstetrical management (eg, antenatal
corticosteroids), the liberal use of planned late preterm cesarean delivery, and improved neonatal care.
Neonatal anemia is also increased in pregnancies with placenta previa [86,87].
Morbidity of low-lying placenta — The morbidity of low-lying placenta (placental edge is <2 cm from, but not
over, the internal os) is less than that for placenta previa and decreases as the distance between the placental
edge and internal cervical os increases. A study that compared pregnancy outcomes of 53 women with placental
edge 1 to 10 mm versus 11 to 20 mm from the internal cervical os reported the following [88]:
RECURRENCE — Placenta previa recurs in 4 to 8 percent of subsequent pregnancies [16].
MANAGEMENT — (See "Placenta previa: Management".)
INFORMATION FOR PATIENTS — UpToDate offers two types of patient education materials, "The Basics" and
"Beyond the Basics." The Basics patient education pieces are written in plain language, at the 5 to 6 grade
reading level, and they answer the four or five key questions a patient might have about a given condition. These
articles are best for patients who want a general overview and who prefer short, easy-to-read materials. Beyond
the Basics patient education pieces are longer, more sophisticated, and more detailed. These articles are written
at the 10 to 12 grade reading level and are best for patients who want in-depth information and are
comfortable with some medical jargon.
Preterm delivery <37 weeks (44 percent, relative risk [RR] 5.32, 95% CI 4.39-6.45)●
Neonatal intensive care unit admission (RR 4.09, 95% CI 2.80-5.97)●
Neonatal death (RR 5.44, 95% CI 3.03-9.78)●
Perinatal death (RR 3.01, 95% CI 1.41-6.43)●
Antepartum hemorrhage: 29 versus 3 percent●
Postpartum hemorrhage: 21 versus 10 percent●
Preterm birth: 29 versus 3 percent●
Cesarean delivery: 75 versus 31 percent●
th th
th th
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Here are the patient education articles that are relevant to this topic. We encourage you to print or e-mail these
topics to your patients. (You can also locate patient education articles on a variety of subjects by searching on
"patient info" and the keyword(s) of interest.)
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REFERENCES
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Basics topics (see "Patient education: Placenta previa (The Basics)")●
One to 6 percent of pregnant women display sonographic evidence of a placenta previa between 10 and 20
weeks of gestation when they undergo routine obstetrical ultrasound examination. The majority of these
women are asymptomatic and 90 percent of these early cases resolve. (See 'Asymptomatic finding on
midtrimester ultrasound examination' above.)
●
The characteristic symptom of placenta previa is painless vaginal bleeding, which occurs in up 90 percent of
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bleeding, similar to the presentation of abruptio placenta. In approximately one-third of pregnancies with
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●
Placenta previa should be suspected in any woman beyond 20 weeks of gestation who presents with
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examination is performed because palpation of the placenta can cause severe hemorrhage. (See 'Diagnosis'
above.)
●
The diagnosis of placenta previa is based on identification of placental tissue over the internal cervical os on
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●
Previous placenta previa, previous cesarean deliveries, and multiple gestation are major risk factors for
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●
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●
Some conditions that may be associated with placenta previa include placenta accreta, malpresentation,
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●
When placenta previa is diagnosed, the possibility of placenta previa-accreta/percreta should be considered
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●
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GRAPHICS
Complete placenta previa
Transabdominal study shows the placenta completely covering the internal os (arrow). A
central placenta previa occurs when the internal os is approximately equidistant from the
anterior and posterior placental edges; 20 to 30 percent of complete previas are central.
Courtesy of Deborah Levine, MD.
Graphic 74665 Version 4.0
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Low lying placenta
Transvaginal study shows a posterior placenta with the tip of the placenta on the internal
os (arrow). The placenta is adjacent to the internal os, but does not cover it.
Courtesy of Deborah Levine, MD.
Graphic 55703 Version 4.0
16. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate
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Overdistended bladder mimicking placenta previa
Transabdominal study shows an over-distended bladder giving the appearance of a previa
in a patient with NO placenta previa. An over-distended bladder can compress the
anterior lower uterine segment against the posterior lower uterine segment, thereby
mimicking placenta previa. The arrow points to the cervical os.
Courtesy of Deborah Levine, MD.
Graphic 76545 Version 3.0
17. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate
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Contributor Disclosures
Charles J Lockwood, MD, MHCM Nothing to disclose Karen Russo-Stieglitz, MD Nothing to
disclose Deborah Levine, MD Nothing to disclose Vincenzo Berghella, MD Nothing to disclose Vanessa A
Barss, MD, FACOG Nothing to disclose
Contributor disclosures are reviewed for conflicts of interest by the editorial group. When found, these are
addressed by vetting through a multi-level review process, and through requirements for references to be
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