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Placental Blood Drainage Shortens Duration of the Third Stage of Labor in Women Slowly Administered 20 IU Oxytocin

Authors:
  • zekai tahir burak women's health education and research hospital

Abstract

Objective: Prolongation of the third stage of labor may cause serious postpartum complications. Thus, timely expulsion of the placenta is essential for preventing complications of the third stage of labor. We conducted a prospective cohort study to determine the effect of placental cord drainage on the duration of the TSL in women administered intravenous oxytocin during this stage. Study Design: This was a prospective cohort study in which 112 low risk pregnant women were allocated to the study. There were 53 women in the placental cord drainage group, and 59 women in the cord clamping group without drainage. Immediately after fetal delivery, intravenous infusion of 20 IU oxytocin in 500 mL Ringers’ Lactate was started and infused within 2 hours in women in both groups. Outcome measures were the third stage duration and hemoglobin differences between admission and the postpartum sixth hour. Results: There were no significant differences between the two groups with regard to duration of stages 1 and 2 of labor, hemoglobin level on admission, and at the postpartum sixth hour, and hemoglobin differences between admission and the postpartum sixth hour. The median third stage duration in the study group was 3.40 (range: 0.35-16.20) minutes, and 5.10 (range: 2.30-11.00) minutes in the control group. This difference between the groups was statistically significant (p
1
Experimental
&
Clinical Article
Placental Blood Drainage Shortens Duration of the Third Stage of
Labor in Women Slowly Administered 20 IU Oxytocin
Metin KABA1, Yaprak ENGİN ÜSTÜN1, Elif Gül YAPAR EYİ1, Hakan TİMUR1, Bekir Serdar ÜNLÜ1,
Aysegül ÖKSÜZOĞLU1
Ankara, Turkey
ABSTRACT
OBJECTIVE: Prolongation of the third stage of labor may cause serious postpartum complications.
Thus, timely expulsion of the placenta is essential for preventing complications of the third stage of labor.
We conducted a prospective cohort study to determine the effect of placental cord drainage on the du-
ration of the TSL in women administered intravenous oxytocin during this stage.
STUDY DESIGN: This was a prospective cohort study in which 112 low risk pregnant women were al-
located to the study. There were 53 women in the placental cord drainage group, and 59 women in the
cord clamping group without drainage. Immediately after fetal delivery, intravenous infusion of 20 IU
oxytocin in 500 mL Ringers’ Lactate was started and infused within 2 hours in women in both groups.
Outcome measures were the third stage duration and hemoglobin differences between admission and
the postpartum sixth hour.
RESULTS: There were no significant differences between the two groups with regard to duration of
stages 1 and 2 of labor, hemoglobin level on admission, and at the postpartum sixth hour, and hemo-
globin differences between admission and the postpartum sixth hour. The median third stage duration in
the study group was 3.40 (range: 0.35-16.20) minutes, and 5.10 (range: 2.30-11.00) minutes in the con-
trol group. This difference between the groups was statistically significant (p<0.01).
CONCLUSION: Placental cord drainage reduces the third stage duration following vaginal deliveries in
patients receiving intravenous oxytocin. Placental cord drainage is simple, does not require additional
cost, and is applicable for every delivery.
Keywords: Third stage of labori, Active management of the third stage, Placental cord drainage,
Oxytocin, Expectant management
1Department of Obstetrics and Gynecology Zekai Tahir Burak Women’s
Health Education and Research Hospital, Ankara
Address of Correspondence: Metin Kaba
Akdeniz University Faculty of Medicine
Department of Obstetrics and
Gynecology Antalya, Turkey
metinkaba12@hotmail.com
Submitted for Publication: 11.07.2016
Accepted for Publication: 20.09.2016
Obstetrics; Maternal Fetal Neonatal Medicine
Gynecol Obstet Reprod Med 2016;22 (Article in Press)
Introduction
The third stage of labor (TSL) is defined as the time inter-
val between delivery of the baby and the expulsion of the pla-
centa. After delivery of the baby, health care providers usually
give attention to the newborn. But this stage is also important
for the woman who gave birth. Prolongation of the TSL leads
to an increased likelihood of maternal morbidity and mortality
and TSL-related complications, which include uterine atony,
retained placenta, postpartum hemorrhage (PPH), hemor-
rhagic shock, and even maternal death (1,2). Reported child-
birth-related maternal mortality is approximately 250.000 and
300.000 in the world annually (3). The majorities of these
mortalities are caused by complications during the TSL, and
most commonly are from uterine atony and PPH (3). The
timely expulsion of the placenta and an efficient uterine con-
traction to cease bleeding are important parts of the TSL in
preventing complications. Placental delivery is essential in al-
lowing the uterus to contract and decrease blood loss during
the TSL. Placental expulsion depends on the separation of the
placenta from the uterine wall, capillary hemorrhage, uterine
muscle contractile ability after placental separation, maternal
effort, and gravity of the placenta (4,5). Separation of the pla-
centa from the uterine wall is usually completed within 15
minutes in 90% of women after a fetal delivery (2,6).
Gynecology Obstetrics & Reproductive Medicine 2016;22:0 2
Prolongation of the TSL increases the development of PPH,
which is responsible for one quarter of maternal deaths glob-
ally, one third of all pregnancy-related deaths in Africa and
Asia, and approximately 140.000 deaths annually (7,8).
Preventive measures to decrease complications from the
TSL are recommended for all women undergoing childbirth
(9). Interventions to prevent TSL complications are called ac-
tive management of the third stage of labor (AMTSL). These
interventions include early umbilical cord clamping, adminis-
tration of an oxytocic agent, and controlled cord traction until
delivery of the placenta (3,8). Placental cord drainage is also
considered as an AMTSL method. Placental cord drainage fa-
cilitates placental delivery in both vaginal and cesarean sec-
tion deliveries (10,11). Releasing the maternal side of the cord
clamp and allowing the drainage of placental blood has been
recommended by many obstetricians to facilitate the delivery
of the placenta in vaginal deliveries (11).
We conducted this prospective cohort trial to determine
whether placental cord drainage would shorten the TSL dura-
tion in low-risk pregnant women receiving 20 IU oxytocin in
500 mL Ringer’s Lactate (RL) intravenous infusion (IV)
within 2 hours.
Material and Method
This study was undertaken between 1 February and 30
June 2010 in the obstetric unit of the Zekai Tahir Burak
Women's Health Education and Research Hospital, Ankara,
Turkey. The study was approved by the Institutional Ethics
Committee and performed in accordance with the Helsinki
Declaration (Institutional ethical approval no: 19/04/2010/6).
On admission to the labor room, a detailed history, vaginal
examination, and blood count estimation were carried out with
all patients. Eligible patients were informed about the study
and written informed consent was obtained from each patient.
A total of 112 women who had a vaginal delivery completed
the trial. There were 53 (47.3%) women in the study group
and 59 (52.6%) in the control group. Inclusion criteria were
singleton cephalic presentation pregnancies, patients willing
to give written informed consent and pregnancies between 37
and 42 weeks of gestational age. Exclusion criteria were in-
trauterine fetal demise, antepartum hemorrhage, malpresenta-
tion, hypertensive disorders, history of medical disorders,
multiple pregnancy, chorioamnionitis, and coagulation abnor-
malities. Fetal and maternal monitoring during the first and
second stages of labor were carried out. In cases where aug-
mentation or induction of labor was indicated, an oxytocin in-
fusion protocol was applied.
When the cervix was dilated to 10 cm and the fetus arrived
at the perineum, the pregnant woman was transferred to the
delivery ward. Following delivery of the neonate, the umbili-
cal cord was clamped with two clamps, cut between the
clamps, and the neonate was handed to the nurse who was ed-
ucated for neonatal care. In the placental cord drainage group,
after the cord was clamped and cut, immediate unclamping
was performed on the maternal side of the cord and the blood
in the placenta was allowed to drain freely. In the control
group, the umbilical cord remained clamped until placental
delivery. Immediately after fetal delivery, intravenous infusion
of 20 IU oxytocin in 500 mL RL was started and transfused
within 2 hours for women in both groups. Upon observing
signs of placental separation (gush of blood from the vagina,
descent of the umbilical cord, and an increase in the height of
the uterus in the abdomen as the lower segment distends) and
once the placenta came into the vagina, it was pulled out. The
duration of the TSL was determined with a watch controlled
by the same physician. Complete removal of the placenta and
membranes was then confirmed. Any adverse event such as a
prolonged third stage, a retained placenta, uterine atony, post-
partum hemorrhage, and any vaginal tear was noted. If the pla-
centa was not delivered after 30 minutes, it was considered a
retained placenta. After completion of the TSL, the woman
was transferred to the recovery room. Maternal pulse, blood
pressure, and temperature were recorded within 15 minutes in
the first hour and then hourly for the following six hours. At
the postpartum sixth hour, a blood sample was taken to evalu-
ate maternal hemoglobin levels.
All statistical analyses were performed using the Statistical
Package for Social Sciences software, version 15.5 (SPSS,
Chicago, IL, USA). Student’s t-test and Mann-Whitney U test
were used for statistical analyses. Parametric test results are
presented as mean ± standard deviation; nonparametric test re-
sults are presented as a median with minimum and maximum
values. The probability of the null hypothesis was set to a 0.05
value. From a total of 112 women, data were analyzed from 53
women in the placental drainage with oxytocin group and
from 59 women in the oxytocin alone group.
Results
Demographic characteristics of the women in the two
groups were similar with regard to age, body mass index
(BMI), gravidity, parity, weeks of gestation, and fetal birth
weight; thus, these results demonstrate that the groups were
similar to each other and comparable (Table 1). There was no
significant difference between the groups with regard to the
duration of the first and second stages of labor with p values
of 0.226 and 0.105, respectively. However, the duration of the
TSL was significantly shorter in the placenta drainage group
than in the oxytocin alone group (p <0.01) (Table 2). In the
oxytocin alone group, there was a single placental retention
that was extracted with manual intervention under general
anesthesia.
3Kaba M. Engin Üstün Y. Yapar Eyi EG. Timur H. Ünlü BS. Öksüzoğlu A.
Discussion
The present study demonstrated that placental cord
drainage shortens the duration of the third stage of labor in
women who were administered an intravenous infusion of 20
IU oxytocin. Prolonged TSL is the major cause of maternal
morbidity and mortality worldwide (12). When the TSL is
prolonged, uterine contractile abilities may decrease and
blood flow from uterine vessels to the placental bed continues.
Inefficient uterine contraction may lead to excessive blood
loss from the placental bed and result in PPH (1,13). PPH is
commonly defined as a blood loss of 500 mL or more within
24 hours of giving birth (14). Although it is almost entirely a
preventable condition, PPH is the most serious complication
in obstetric practices, occurs in approximately 4% of vaginal
deliveries, and is the major cause of maternal deaths from
hemorrhage during childbearing (16). Two thirds of PPH cases
occur in women with no previously known risk factors. Thus,
all pregnant women are considered to be at risk for this condi-
tion (17). The degree of blood loss associated with placental
separation and delivery depends on how quickly the placenta
separates from the uterine wall and how effectively the uterine
muscle contracts around the placental bed and the uterine
blood vessels (3). If the placenta is not delivered within 10
minutes, the risk of PPH increases (18). Therefore, any inter-
vention for shortening the duration of the TSL and preventing
complications becomes important. AMTSL decreases the du-
ration of TSL, decreases maternal blood loss, decreases the
likelihood of uterine atony, and reduces the incidence of PPH
by approximately 65% when compared with expectant man-
agement (1,2,3,19). Therefore, the International Federation of
Gynecologists and Obstetricians, the International
Confederation of Midwives, and the World Health
Organization recommend the routine use of AMTSL for all
vaginal singleton births (20).
Active management of the third stage of labor with utero-
tonic drugs for preventing complications during the TSL is
recommended for all births (21). Oxytocin can be adminis-
tered IV or intramuscularly (IM) with fewer side effects.
Prophylactic oxytocin, at any dose, decreases the development
of uterine atony, PPH, and the need for therapeutic uterotonic
drugs (21). Therefore, oxytocin is universally recommended
as the first-line uterotonic drug of choice for the prevention of
uterine atony and related complications (8). Additionally, oxy-
tocin has a short half-life (3 minutes) and using oxytocin dur-
ing the first and second stages of labor has no effect on TSL.
Therefore, AMTSL should be recommended for all women
during vaginal delivery regardless of whether they received
oxytocin or not during the first and second stages of labor (2).
For this reason, in the present study, we did not regard the use
of oxytocin in the first and second stages of labor.
Although oxytocin could be administrated IV/IM, the most
efficient route of oxytocin administration is a slow IV infusion
or a bolus infusion given over 1–2 minutes (21,22). Oxytocin
acts quickly and effectively with minimal adverse effects and
can be used in all women, which makes it the main interven-
Table 1: Demographic characteristics of the two groups
Variables Cord drainage (n=53) Oxytocin alone (n=59) p value
Age 25.8±4.3 27±5.4 0.30a
BMI 27.7 6±3.51 28.17±3.57 0.56a
Gravity 2 (1-10) 2 (1-5) 0.79b
Parity 1 (0-4) 1 (1-3) 0.37b
Gestational ages (weeks) 39.3±1.3 39±1.5 0.29a
Birth weight (gram) 3360±370.1 3357.9±562.4 0.92a
Data presented as mean ± standard deviation or median with minimum maximum
BMI: Body mass index, a: Student t test, b: Mann-Whitney U-test
Table 2: Comparison of duration of labor stages and hemoglobin values between the two groups
Variables Cord drainage (n=53) Oxytocin alone (n=59) p value
Stage 1 (hour) 8 (2-25) 8.5 (3-22) 0.27b
Stage 2 (minute) 15 (5-90) 10 (5-120) 0.11b
Stage III (minute) 3.4(0.35-16.2) 5.10 (2.3-11) <0.01b
Hemoglobin level on admission 12.3±1.3 12.3±1.1 0.89a
Hemoglobin level at postpartum 6th hours 11.6±1.3 11.6±1.2 0,95a
Hemoglobin differences between on admission and
postpartum 6th hours (mg/dL) 0.6 (0.3-2.6) 0.6 (0.1-1.2) 0.17b
Data presented as mean ± standard deviation or median with minimum maximum values.
a: Student t test, b: Mann-Whitney U-test
Gynecology Obstetrics & Reproductive Medicine 2016;22:0 4
tion for reducing PPH and is the first uterotonic drug option
(23). The administration of oxytocin during the TSL reduces
the risk of PPH by 40% (24). Immediately after fetal delivery,
starting intravenous infusion of 20 IU of oxytocin in 500 mL
RL and given within 2 hours is the routine protocol in our in-
stitute for AMTSL. This routine protocol was administered to
both groups so as not to sustain any adverse effects of not
using an appropriate AMTSL. This may explain why PPH or
uterine atony did not develop, and the median duration of the
TSL was shorter in both groups than previously reported ex-
pectant management.
It has been reported that placental cord drainage shortens
the duration of TSLs. Giacalone et al. reported that in their
randomized control study comparing placental cord drainage
with expectant delivery of the placenta, the median TSL dura-
tion was 8 minutes in the placental cord drainage group and 15
minutes in the control group (25). Roy et al. reported that pla-
cental blood drainage during vaginal delivery shortens the du-
ration of TSL, reduces both the blood loss and the incidence
of PPH (26). Shravage et al. reported in their randomized con-
trolled study that the average TSL duration was significantly
shorter in the placental cord drainage group than in the control
group. Sharma et al. performed a randomized study in which
placental cord drainage was compared with placental cord
traction during cesarean sections. They found that placental
cord drainage shortened the TSL duration and reduced the re-
tained placenta rate (10). In another study, Sharma et al. com-
pared placental cord drainage with controlled cord traction
after the administration of 0.2 mg of ergonovine with the de-
livery of the anterior shoulder and immediate cord clamping to
compare PPH and TSL length. They reported that placental
cord drainage significantly reduces the TSL duration in vagi-
nal deliveries (11). A 2011 Cochrane review reported that pla-
cental cord drainage significantly shortens TSL and decreases
the average blood loss. The authors’ concluded that there was
a small reduction in the TSL length and in the amount of blood
loss when cord drainage was compared with no cord drainage
(27). In the present study, placental cord drainage shortened
the TSL duration. This result is in accordance with the results
from previous studies.
Herman et al. ultrasonographically demonstrated that a
retro-placental myometrial contraction is mandatory to pro-
duce shearing forces on the interface between the placenta and
the myometrium to supply placental separation (5,28).
Contractions occurring prior to delivery are insufficient to
cause placental separation since, in the presence of the fetus,
the myometrium is unable to achieve the necessary strain for
placental separation (5,28). Placental cord drainage is likely to
decrease placental volume and surface area that might facili-
tate placental separation and uterine contraction, which results
in a further increase of the separated area. This facilitates uter-
ine contraction and further placental separation, resulting in
early placental delivery and a shortening of the TSL duration.
This may explain why the TSL was shorter in the placental
cord drainage group in the current study.
Placental retention is defined as the failure of placental de-
livery within 30 to 45 minutes and it usually requires inter-
vention to assist delivery (18). Failure of the retro-placental
myometrium contraction is the usual cause of a retained pla-
centa. When the duration of a placental retention increases to
30 minutes, there is a greater risk of PPH (5). Placental cord
drainage may facilitate uterine contractions and shorten the
TSL. In the present study, there was no placental retention in
the study group, and only one in the control group, which was
expulsed with manual intervention under general anesthesia.
This may explain why the placental retention rate was de-
creased in the placental cord drainage group in both the pres-
ent study and previous studies.
Blood loss during TSL was not estimated in the present
study. In previous studies, blood losses were estimated using
difference methods. During blood collection at TSL, some
amniotic fluid might enter the collection bag, or there may be
an omission of blood that spattered on drapes and gowns.
Thus, the measurement remains open to inaccuracies that can
especially affect the measurement of lower amounts of blood
loss (17). Additionally, three guidelines from the American
College of Obstetrician and Gynecologists, the Royal College
of Obstetrician and Gynecologists, and the Society of
Obstetricians and Gynecologists of Canada comment on the
unreliability of estimated blood loss, such as using a visible
estimate or through the use of blood collection drapes (8).
Instead of attempting blood collection to measure blood
losses, we compared hemoglobin differences between the pa-
tient at admission and at their postpartum sixth hour. We know
from previous studies that shortening the TSL duration also
decreases blood loss.
The present study demonstrated that placental blood
drainage with oxytocin shortened the TSL duration compared
to oxytocin alone. Placental blood drainage is simple, does not
introduce any additional cost, and can be performed by any
birthing attendant. It might be used alone where uterotonic
agents were not available or combined with oxytocin for
AMTSL in low-risk vaginal deliveries. Because of the small
sample size, this study is limited in its ability to derive a de-
finitive result and generalize the results to the entire popula-
tion. Furthermore, well-randomized studies with large sample
sizes are needed to evaluate the effectiveness of placental cord
drainage with IV oxytocin administration in the TSL.
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... They stated that the 3 rd stage duration was significantly lower in PCD than no PCD group. Fourth, Kaba et al., [25] who studied the combination of PCD with 20 IU oxytocin on the 3 rd stage duration. They stated that the median 3 rd stage duration in the study group was 3.40 minutes compared to 5.10 minutes in the control group. ...
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Background: Postpartum hemorrhage (PPH) is accountable for around 25% of maternal mortality in the developing countries. Management of 3 rd stage of labour is the cornerstone in PPH prevention. The effect of Placenta Cord Drainage (PCD) on the 3 rd progress and PPH prevention is still controversy. Aim of the study: This study aims to investigate the effect of placental drainage on the third stage of labour progress and incidence of postpartum hemorrhage. Research design: randomized controlled clinical trial. Setting: This study is conducted at normal labour unit at Damanhour educational institution affiliated to ministry of health at Elbehira governorate/Egypt. Sampling: A purposive sample of 120 women undergoing normal easy vaginal delivery. Tools: two tools were used for data collection. Tool I: sociodemographic characteristics and obstetric history interview schedule. Tool II: Labour assessment sheet it consists of three main parts. Part I: Summary of the first and second stage of labor. Part II: third stage assessment sheet. Part III: 3. Early postpartum assessment sheet. Results: The present study results shows no statistical significant differences between PCD and control group regarding vital signs during the 3rd stage, uterus condition after placenta delivery, type, dose and route of uterotonic drugs given during 3rd stage. On the contrary, a statistical significant reduction in the time elapsed until appearance of placenta separation signs (3.5583±0.83915), 3rd stage duration(5.1417±1.03138), amount of blood loss during 3rd stage (195.45±13.994), placenta weight (580.333±64.97631) and incidence of retained placenta ((0%) in the PCD group than control. In the early postpartum assessment, the mean pulse (88.2.7667±3.11022) is higher among control group compared to PCD (83.4667±2.78292) group. Control group needs higher dose of uterotonic (8.6780±2.62902) drugs than PCD (5.0566±1.41985) group. In addition, maternal hemoglobin (9.5234±0.6087) is slightly higher in PCD group compared to control (8.458±0.873). Conclusion: PCD is safe, effective noninvasive intervention that may help in improving 3 rd stage progress. Recommendation: PCD should be added to third stage of labour intervention protocol.
... They noticed mean change in hemoglobin 0.6 gm% in study group and 1.1 gm% in control group.6 A study by Metin KABA et al 2016, on placental blood drainage reported a change in hemoglobin 0.6 gm% in both groups.10 ...
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Background: In placental cord drainage facilitates placental delivery in both vaginal and caesarean section deliveries. The present study was done to evaluate the effect and safety of placental blood drainage as a part of active management of third stage of labour to reduce the duration and blood loss during third stage of labour.Methods: The study was conducted in department of Obstetrics and, SN Medical College, Agra, Uttar Pradesh, India on 400 term pregnant women, with single live intrauterine fetus in cephalic presentation, without any complication. They were randomly divided into to study and control group. Study group: It comprised of 200 Gynaecology cases, underwent active management of third stage of labour with placental blood drainage. Control group: It comprised of 200 cases, underwent active management of third stage of labour (AMTSL) alone. Duration and blood loss during third stage were noted.Results: The mean duration of third stage of labour was 3.61±0.972mins in study group and 8.15±1.711mins in control group. The mean blood loss during third stage of labour was 168.14±76.703ml and 287.40±85.808ml in study and control group respectively.Conclusions: Duration of third stage, blood loss during third stage, and hemoglobin deference between pre and post-delivery were reduced significantly in study group than control group.
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Background: Postpartum hemorrhage is the leading cause associated with 25% of maternal mortality. Prolonged duration of third stage of labour accounts for postpartum hemorrhage. The new trend in third stage management is placenta cord drainage (PCD). The physiology of PCD is decrease in bulkiness of placenta which consequently increases the uterine contractility. Effective uterine contraction mostly shortens third stage duration and decrease the risk for PPHMethods: This study is a randomized control trial in which full term pregnant women admitted in labour unit at Sri Devaraj Urs medical college and research centre, Kolar, Karnataka. Total 80 women were included in this study. They were divided into two groups, control group and study group with n=40 in each group. Placental cord drainage was done in the study group. In the Group 1 placental end of the cut umbilical cord remained clamped. In the Group 2, the placental end of the cut umbilical cord unclamped immediately and collected in a vessel till the flow ceased. Thus, the drained blood was prevented from getting mixed with blood lost in the third stage. Blood lost in the third stage was collected in a clean drape sheet. Placenta was delivered by controlled cord traction after the signs of placental separation were seen. The duration of third stage was calculated using a stopwatch.Results: In our study, the mean duration of third stage of labour in control group was 6.58minute and in study group was 2.28 minutes. Significant statistical difference was found in duration of third stage of labour.Conclusions: PCD is noninvasive and safe intervention during third stage of labour and effective in reduction of incidence of postpartum hemorrhage.
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Objective To document the use of active management of the third stage of labour for preventing postpartum haemorrhage and to explore factors associated with such use in seven developing countries. Methods Nationally representative samples of facility-based deliveries were selected and observed to determine the use of active management of the third stage of labour and associated factors. Policies on active management were assessed through document review and interviews with relevant professionals. Findings Use of a uterotonic during the third or fourth stages of labour was nearly universal. Correct use of active management of the third stage of labour was found in only 0.5% to 32% of observed deliveries due to multiple deficiencies in practice. In every country except Indonesia, policies regarding active management were conflicting. Conclusion Developing countries have not targeted decreasing postpartum haemorrhage as an achievable goal; there is little use of active management of the third stage of labour, and policies regarding such management often conflict. Studies are needed to identify the most effective components of active management so that the most efficient package of practices can be promoted. Une traduction en français de ce résumé figure à la fin de l'article. Al final del artículo se facilita una traducción al español.
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Aim The third stage of labour commences after the delivery of the foetus and ends with the delivery of the placenta and its membranes. Postpartum haemorrhage is the most common cause of maternal mortality and accounts for about 25 % of maternal deaths in India. Objectives The present study was designed to evaluate the effectiveness of placental blood drainage after spontaneous vaginal delivery as part of active management of third stage of labour in decreasing the duration, blood loss, and complications of the third stage, against no drainage of placental blood. Methodology Two hundred pregnant patients with 37 or more weeks of gestation, with single live foetus in cephalic presentation, who underwent a spontaneous vaginal delivery, were included in the study. The patients were prospectively randomized equally into two groups (100 each in the study and control groups). Placental blood was drained in all the patients in the study group, whereas in the control group the cord blood was not drained. Blood lost in the third stage of labour was measured by collecting in a disposable conical measuring bag, and blood from the episiotomy was mopped, and the mops were discarded separately. Results The baseline statistics in both the group were comparable. The duration of third stage of labour was 210.5 s in the study group and 302.5 s in the control group. The ‘p’ value was statistically significant (p ≤ 0.0001). The mean blood loss in study group was 227.5 ml and was 313.3 ml in the control group (p ≤ 0.0001). The incidence of postpartum haemorrhage was 1 % in study group and 9 % in control group. The mean drop in Hb % level was 0.6 gm/dl in study group and 1.1 gm/dl in control group. These above differences were both statistically significant. Conclusion Placental blood drainage as part of active management of third stage of labour was effective in reducing the duration, the blood loss, and also the incidence of PPH. Placental blood drainage is a simple, safe, and non-invasive method of managing the third stage of labour, which can be practiced in both tertiary care centres as well as rural setup in addition to the routine uterotonics.
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To evaluate the success rate of Bakri balloon tamponade (BBT) for managing postpartum hemorrhage (PPH), intractable to conservative medical treatment, as a fertility sparing intervention. We evaluated 47 women treated with BBT who had severe postpartum hemorrhage and uncontrollable bleeding due to failed treatment with uterotonic agents. The main outcome measure was successful management and preservation of the uterus. Forty-seven women were identified for BBT treatment due to severe PPH. BBT was used to successfully manage hemorrhage in 43 patients, and there was no need for hysterectomy. Four patients required an additional surgical procedure. Of the four failures, a subtotal hysterectomy was performed in two patients, and the other two patients underwent a total hysterectomy. The overall success rate was 91.4%, which was comparable to rates reported earlier. The main cause of PPH was uterine atony (43%). Uterine preservation is an important issue when managing PPH. BBT is an effective, easy to use, and safe procedure for massive PPH that can minimize recourse to hysterectomy after failed medical treatment. Copyright © 2015. Published by Elsevier B.V.
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Background: Data for the causes of maternal deaths are needed to inform policies to improve maternal health. We developed and analysed global, regional, and subregional estimates of the causes of maternal death during 2003-09, with a novel method, updating the previous WHO systematic review. Methods: We searched specialised and general bibliographic databases for articles published between between Jan 1, 2003, and Dec 31, 2012, for research data, with no language restrictions, and the WHO mortality database for vital registration data. On the basis of prespecified inclusion criteria, we analysed causes of maternal death from datasets. We aggregated country level estimates to report estimates of causes of death by Millennium Development Goal regions and worldwide, for main and subcauses of death categories with a Bayesian hierarchical model. Findings: We identified 23 eligible studies (published 2003-12). We included 417 datasets from 115 countries comprising 60 799 deaths in the analysis. About 73% (1 771 000 of 2 443 000) of all maternal deaths between 2003 and 2009 were due to direct obstetric causes and deaths due to indirect causes accounted for 27·5% (672 000, 95% UI 19·7-37·5) of all deaths. Haemorrhage accounted for 27·1% (661 000, 19·9-36·2), hypertensive disorders 14·0% (343 000, 11·1-17·4), and sepsis 10·7% (261 000, 5·9-18·6) of maternal deaths. The rest of deaths were due to abortion (7·9% [193 000], 4·7-13·2), embolism (3·2% [78 000], 1·8-5·5), and all other direct causes of death (9·6% [235 000], 6·5-14·3). Regional estimates varied substantially. Interpretation: Between 2003 and 2009, haemorrhage, hypertensive disorders, and sepsis were responsible for more than half of maternal deaths worldwide. More than a quarter of deaths were attributable to indirect causes. These analyses should inform the prioritisation of health policies, programmes, and funding to reduce maternal deaths at regional and global levels. Further efforts are needed to improve the availability and quality of data related to maternal mortality.
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Background: Active management of the third stage of labour involves giving a prophylactic uterotonic, early cord clamping and controlled cord traction to deliver the placenta. With expectant management, signs of placental separation are awaited and the placenta is delivered spontaneously. Active management was introduced to try to reduce haemorrhage, a major contributor to maternal mortality in low-income countries. This is an update of a review last published in 2015. Objectives: To compare the effects of active versus expectant management of the third stage of labour on severe primary postpartum haemorrhage (PPH) and other maternal and infant outcomes.To compare the effects of variations in the packages of active and expectant management of the third stage of labour on severe primary PPH and other maternal and infant outcomes. Search methods: For this update, we searched Cochrane Pregnancy and Childbirth's Trials Register, ClinicalTrials.gov and the World health Organization International Clinical Trials Registry Platform (ICTRP), on 22 January 2018, and reference lists of retrieved studies. Selection criteria: Randomised and quasi-randomised controlled trials comparing active versus expectant management of the third stage of labour. Cluster-randomised trials were eligible for inclusion, but none were identified. Data collection and analysis: Two review authors independently assessed the studies for inclusion, assessed risk of bias, carried out data extraction and assessed the quality of the evidence using the GRADE approach. Main results: We included eight studies, involving analysis of data from 8892 women. The studies were all undertaken in hospitals, seven in higher-income countries and one in a lower-income country. Four studies compared active versus expectant management, and four compared active versus a mixture of managements. We used a random-effects model in the analyses because of clinical heterogeneity. Of the eight studies included, we considered three studies as having low risk of bias in the main aspects of sequence generation, allocation concealment and completeness of data collection. There was an absence of high-quality evidence according to GRADE assessments for our primary outcomes, which is reflected in the cautious language below.The evidence suggested that, for women at mixed levels of risk of bleeding, it is uncertain whether active management reduces the average risk of maternal severe primary PPH (more than 1000 mL) at time of birth (average risk ratio (RR) 0.34, 95% confidence interval (CI) 0.14 to 0.87, 3 studies, 4636 women, I2 = 60%; GRADE: very low quality). For incidence of maternal haemoglobin (Hb) less than 9 g/dL following birth, active management of the third stage may reduce the number of women with anaemia after birth (average RR 0.50, 95% CI 0.30 to 0.83, 2 studies, 1572 women; GRADE: low quality). We also found that active management of the third stage may make little or no difference to the number of babies admitted to neonatal units (average RR 0.81, 95% CI 0.60 to 1.11, 2 studies, 3207 infants; GRADE: low quality). It is uncertain whether active management of the third stage reduces the number of babies with jaundice requiring treatment (RR 0.96, 95% CI 0.55 to 1.68, 2 studies, 3142 infants, I2 = 66%; GRADE: very low quality). There were no data on our other primary outcomes of very severe PPH at the time of birth (more than 2500 mL), maternal mortality, or neonatal polycythaemia needing treatment.Active management reduces mean maternal blood loss at birth and probably reduces the rate of primary blood loss greater than 500 mL, and the use of therapeutic uterotonics. Active management also probably reduces the mean birthweight of the baby, reflecting the lower blood volume from interference with placental transfusion. In addition, it may reduce the need for maternal blood transfusion. However, active management may increase maternal diastolic blood pressure, vomiting after birth, afterpains, use of analgesia from birth up to discharge from the labour ward, and more women returning to hospital with bleeding (outcome not pre-specified).In the comparison of women at low risk of excessive bleeding, there were similar findings, except it was uncertain whether there was a difference identified between groups for severe primary PPH (average RR 0.31, 95% CI 0.05 to 2.17; 2 studies, 2941 women, I2 = 71%), maternal Hb less than 9 g/dL at 24 to 72 hours (average RR 0.17, 95% CI 0.02 to 1.47; 1 study, 193 women) or the need for neonatal admission (average RR 1.02, 95% CI 0.55 to 1.88; 1 study, 1512 women). In this group, active management may make little difference to the rate of neonatal jaundice requiring phototherapy (average RR 1.31, 95% CI 0.78 to 2.18; 1 study, 1447 women).Hypertension and interference with placental transfusion might be avoided by using modifications to the active management package, for example, omitting ergot and deferring cord clamping, but we have no direct evidence of this here. Authors' conclusions: Although the data appeared to show that active management reduced the risk of severe primary PPH greater than 1000 mL at the time of birth, we are uncertain of this finding because of the very low-quality evidence. Active management may reduce the incidence of maternal anaemia (Hb less than 9 g/dL) following birth, but harms such as postnatal hypertension, pain and return to hospital due to bleeding were identified.In women at low risk of excessive bleeding, it is uncertain whether there was a difference between active and expectant management for severe PPH or maternal Hb less than 9 g/dL (at 24 to 72 hours). Women could be given information on the benefits and harms of both methods to support informed choice. Given the concerns about early cord clamping and the potential adverse effects of some uterotonics, it is critical now to look at the individual components of third-stage management. Data are also required from low-income countries.It must be emphasised that this review includes only a small number of studies with relatively small numbers of participants, and the quality of evidence for primary outcomes is low or very low.
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Postpartum haemorrhage (PPH) is one of the leading causes of maternal morbidity and mortality around the world. In the UK, the Centre for Maternal and Child Enquiries (CMACE) confirmed a reduction in maternal deaths due to postpartum haemorrhage during the last Triennium (2006-2008). However, substandard care continues to contribute to more than half of maternal deaths due to postpartum haemorrhage.Primary PPH is defined by the Royal College of Obstetricians and Gynaecologists (RCOG) Green Top Guideline on Postpartum Haemorrhage as a blood loss of 500 ml or more within 24 hours of the birth. It is further classified into minor (500-1000 ml) or major (>1000 ml) with a further sub classification into moderate (1000-2000 ml) or severe (>2000 ml or >30%of blood volume). Secondary PPH is defined as excessive bleeding between 24 hours and 12 weeks postnatally. A timely, multi-disciplinary and systematic approach to restore the volume and clotting system whilst arresting bleeding is essential to improve maternal morbidity and mortality.Although in some cases, massive obstetric haemorrhage can be anticipated and prevented, such as morbidly adherent placenta, it often occurs unexpectedly in women considered at 'low risk'. Hence, all clinicians involved in the care of women during pregnancy and delivery should have the knowledge and skills to promptly recognize symptoms, signs and complications of PPH and immediately activate the appropriate protocol which could save lives.
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To compare four national guidelines for the prevention and management of postpartum hemorrhage (PPH). We performed a descriptive analysis of guidelines from the American College of Obstetrician and Gynecologists (ACOG) practice bulletin, Royal Australian and New Zealand College of Obstetricians and Gynaecologists (RANZOG), Royal College of Obstetrician and Gynaecologists (RCOG), and Society of Obstetricians and Gynaecologists of Canada (SOGC) on PPH to determine differences, if any, with regard to definitions, risk factors, prevention, treatment, and resuscitation. PPH was defined differently in all four guidelines. Risk factors emphasized in the guidelines which conferred a high risk of catastrophic bleeding (e.g. previous cesarean delivery and placenta previa). All organizations except ACOG recommended active management of the third stage of labor (AMTSL) for primary prevention of PPH in all vaginal deliveries. Oxytocin was universally recommended as the medication of choice for PPH prevention in vaginal deliveries. RANZOG and RCOG recommended development of a massive transfusion protocol to manage PPH resuscitation. Recommendations for non-surgical treatment strategies such as uterine packing, and balloon tamponade varied across all guidelines. All organizations recommended transfer to a tertiary care facility for suspicion of abnormal placentation. Specific indications for hysterectomy were not available in any guideline, with RCOG recommending hysterectomy 'sooner rather than later' with the assistance of a second consultant. Substantial variation exists in postpartum hemorrhage prevention and management guidelines among four national organizations, highlighting the need for better evidence and more consistent synthesis of the available evidence with regard to a leading cause of maternal mortality. Copyright © 2015 Elsevier Inc. All rights reserved.
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Postpartum haemorrhage (PPH) remains a major cause of maternal deaths worldwide, and is estimated to cause the death of a woman every 10 minutes. This review presents the latest clinical advice, including new evidence on controlled cord traction, misoprostol, and oxytocin. The controversy around the diagnosis of PPH, the limitations of universal prophylaxis, and novel ways to provide obstetric first aid are also presented. It ends with a call to develop high-quality front-line obstetric services that can deal rapidly with unexpected haemorrhages as well as minimising blood loss at critical times: major abruption, placenta praevia, and caesarean for prolonged labour.
Article
OBJECTIVE(S) : To evaluate the effectiveness of placental blood drainage via the umbilical cord in reducing the duration of blood loss in third stage of labor, and the incidence of postpartum hemorrhage. METHOD(S) : A randomized controlled trial was carried out on 200 pregnant women. In the study group the placental end of the cut umbilical cord was unclamped immediately after it was cut and in the control group it remained clamped. Placenta was delivered by controlled cord traction. Intravenous methergin was given after delivery of placenta in both the groups. The duration of third stage and the amount of blood loss were noted. The results were analysed by 'Z' test and unpaired 't' test. RESULTS : The duration of third stage was 5 minutes in the study group and 7.4 minutes in the control group. This difference was statistically significant (P<0.001). The average third stage blood loss was 175 ml in the study group and 252 ml in the control group. This difference also was statistically significant (P< 0.001). The incidence of postpartum hemorrhage was decreased in the study group (3% vs 10%). None of the women required blood transfusion. CONCLUSION(S) : Placental blood drainage is a simple safe and noninvasive method which reduces the duration of blood loss in third stage thereby preventing postpartum hemorrhage.