A comparative study of oxytocin, carboprost,
methylergometrine and misoprostol in prevention of postpartum haemorrhage a
prospective study
Patil A.S.¹,
Dandavate V.2, Thobbi V.3
1Dr. Ambika S. Patil, Assistant Professor, 2Dr. Vibhavaree
Dandavate, Associate Professor, 3Dr. Vidya Thobbi, Professor and
HOD, all authors are affiliated with Department of OBG, Al Ameen Medical
College, Vijayapur, Karnataka, India.
Corresponding Author: Dr. Vibhavaree Dandavate, Associate Professor, Department of OBG, Al
Ameen Medical College, Vijayapur, Karnataka, India. E-mail:
vibhavaree.dandavate@gmail.com
Abstract
Background: Post partumhemorrhage (PPH) is an important
cause of maternal mortality accounting for nearly 15-20% of maternal deaths in
India. Oxytocic drugs like oxytocin, ergot alkaloids, and various
prostaglandins are being used for active management of third stage of labour. Materials and Methods: A prospective
study was conducted in the Department of Obstetrics and Gynaecology of Al Ameen
Medical College, Vijayapur, in 400 women. Patients were randomized into four
groups of 100 each and were given oxytocic within 60 seconds of delivery
anterior shoulder of the baby. Oxytocics used were 10 IU intramuscular
oxytocin,125 µg intramuscular carboprost, 0.2 mg intravenous methylergometrine,
and 800 µg tablet misoprostol per rectally in groups A, B, C and D
respectively. Results: Duration of
third stage of labor recorded was minimum with carboprost with mean duration of
3.84+/-0.99 minutes and was maximum with methylergometrine with mean duration
of 5.04+/-1.02 minutes. Amount of blood loss observed was minimum with
carboprost (mean 131 +/-72.037 ml) and maximum with Methylergometrine (mean 435+/-147.578
ml). Hemoglobin drop was also seen more with Methylergometrine with mean drop of 0.872+/-0.458 gm% and minimally with carboprost with mean
drop of 0.236 +/-0.221 gm%. Conclusion: It
is concluded from this study that carboprost is the uterotonic of choice
followed by oxytocin for active management of third stage of labor.
Keywords: Postpartum
Hemorrhage, Active Management of Third Stage of Labor, Oxytocic Drugs, Third
stage of labour.
Author Corrected: 25th March 2019 Accepted for Publication: 29th March 2019
Introduction
The third stage of
labour is the most crucial stage, begins with expulsion of baby and ends with
expulsion of placenta and membranes. Its average duration is 15 min in both
primigravida and multigravida [1]. Postpartum hemorrhage is one of the dreaded
complications of third stage of labour. In India every 4 minutes a woman dies
during childbirth [2]. Maternal mortality rate in India is 212 per 100000 live
births. Among them 30% of deaths are due to postpartum hemorrhage (PPH) [3].
Reducing likelihood
of postpartum haemorrhage by routine active management of third stage of labour
could play an important role in reducing maternal mortality and morbidity in
modern obstetrics. The decrease in the problems associated with third stage of
labour has been attributed to judicious use of different oxytocic preparations
administered at time of delivery of anterior shoulder and a transition from
expectant to active intervention [4-5]. Drugs conventionally used for
prophylaxis against PPH includes oxytocin, methylergometrine, misoprostol and
15 methyl PGF2α (Carboprost) [6]. Recent studies have shown that there are
still wide variations in practice around the world in the management of third
stage of labour [7-8]. Prophylactic use of oxytocic agents after delivery of
the infant has been shown to reduce the incidence of PPH by 40%. But it is
associated with side effects ranging from nausea, vomiting, and hypertension to
postpartum eclampsia, intracerebral haemorrhage, myocardial infarction, cardiac
arrest and pulmonary oedema [2]. Carboprost tromethamine is a PGF2 α analogue.
It is given as a single intramuscular injection. It is free from side effects
such as hypertension [9]. Postpartum
haemorrhage is defined as any amount of bleeding following delivery which can
lead to deterioration in the condition of woman. It is difficult to delineate
the risk factors for postpartum haemorrhage. So, all woman are considered at
risk. Active management of third stage of labor has been universally
recommended as not an option but a rule. This includes administration of
uterotonics, controlled cord traction and fundal massage the placenta will be
delivered safely after the delivery of fetus and can prevent postpartum
haemorrhage and maternal deaths.
Aims and Objectives
1. To evaluate and compare the efficacy of
oxytocin, carboprost, methylergometrine and misoprostol in the active
management of third stage of labor and thereby prevention of PPH.
2. To compare the
amount of blood loss in third stage.
3. To compare the
duration of third stage.
4. To evaluate the side
effects
Methods
The present prospective study was conducted
in the Department of Obstetrics and Gynaecology, Al Ameen Medical College,
Vijayapur, over the period from 2017 to 2018 after taking approval from
Institutional Ethical Committee. Four hundred patients were enrolled and these
patients were distributed in four different groups randomly.
Informed consent and counselling of the
patients was done. A detailed history of all the patients was taken including
name, age, parity, socioeconomic status, and menstrual history, period of
gestation (in weeks), obstetrical history including postpartum hemorrhage and
history of any medical disorder. Complete general and systemic examination was
done. Detailed systemic and obstetrical examination was done. Pelvic
examination was done.
After detailed history and examination,
patients were randomized into four groups of 100 each as follows:
Group A-
Patients received 10 IU intramuscular oxytocin.
Group B-
Patients received 125 µg intramuscular carboprost
Group C- Patients
received 0.2 mg intravenous methylergometrine.
Group D-
Patients received 800 µg tablet misoprostol per rectally.
Placebo control is not possible in this study
because we can’t deny a uterotonic to a patient after delivery.
Inclusion Criteria: Women
with singleton pregnancy, Term gestation, without any high risk factors.
Exclusion
Criteria
1. Period of gestation <37weeks and
>42week.
2. Fetal complications: IUFD, IUGR.
3. Maternal complications: PIH, Multiple
pregnancy, Grand multipara, APH, malpresentations, patient with known blood
coagulation disorder, patient with known allergy to prostaglandins, history of
medical disorders– cardiac disease/renal disease, anemia (Hb<7gm%)
Active management of third stage of labor was
done within one minute after the birth of the baby using one of the four
oxytocic drugs as per the group of the patient.
Within a minute of delivery of baby, Brass-V
drapes were immediately applied to measure the amount of blood loss. Placenta
was delivered by controlled cord traction as soon as signs of placental
separation appeared. Inspection of vulva for perineal tears and per speculum
examination for cervical tear was carried out and if present patients were not
taken into series. Repeat haemoglobin estimation was done on second postpartum
day.
Type of study: Prospective
study.
Ethical Approval:
The study was approved by the institutional ethics committee.
Sampling Method: Randomisation
done.
Statistical Methods: The statistical analysis was performed using students t-test and paired
t-test for continuous variables. p-value of <0.05 was considered
statistically significant. Data were calculated as means, standard deviation
(SD), numbers and frequency (%).
No scoring system and surgical procedure
used.
The data were evaluated for the following
1. Duration of third stage of labor in all
groups.
2. Amount of blood loss during third stage of
labor.
3. Drop in mean hemoglobin levels in various
groups.
4. Comparison of the side effects of various
uterotonics.
Results
Patients in all four groups were comparable
with regards to their age, socioeconomic status, parity, booking status, BMI
and number of episiotomies given (Table1).
Mean duration of third stage of labor was
4.72 minutes in group A, 5.04 minutes in group C and 4.93 minutes in group D.
It was lowest in group B (3.84 minutes) which is statistically significant with
p value of 0.002 (Table2) (Graph1).
Mean blood loss in various study groups A, B,
C and D was 223.2, 131.8, 435 and 255.8ml respectively. Maximum blood loss was
in patients given methylergometrine and minimal in patients given Carboprost
with a p-value of <0.001 which is statistically significant (Table 2) (Graph
2).
Groups A, B and D showed comparable drop in
haemoglobin 0.3, 0.2 and 0.4 gm%. The maximal drop was observed in group C up
to 0.8 gm% with a significant p-value of 0.002 (Table2).
However 6 patients in group C had postpartum
hemorrhage (statistically significant with p-value of 0.004) (Table 2).
Two patients out of six who had postpartum
haemorrhage necessitating additional oxytocics and blood transfusion which is
statistically significant with a p-value of 0.111 (Table 2).
Nausea and vomiting were found to be the
commonest side effects in all groups followed by shivering and fever.
Table-1:
Biosocial characteristics of the study subjects
|
Group
A Oxytocin |
Group
B Carboprost |
Group
C Methylergometrine |
Group
D Misoprostol |
p-value |
Mean age (years) |
22.96 |
22.16 |
22.84 |
23.16 |
0.051 |
Booking (%) |
|
|
|
|
|
Booked |
52 |
48 |
44 |
52 |
|
Unbooked |
48 |
52 |
56 |
48 |
0.931 |
Socioeconomic status (%) |
|
|
|
|
|
Upper |
0 |
0 |
0 |
4 |
|
Upper middle |
36 |
32 |
36 |
44 |
0.921 |
Lower middle |
44 |
40 |
40 |
36 |
|
Upper lower |
12 |
24 |
20 |
12 |
|
Lower |
8 |
4 |
4 |
4 |
|
Parity (%) |
|
|
|
|
|
P1 P2 |
64 28 |
72 20 |
76 12 |
56 24 |
0.803 |
P3 |
8 |
8 |
12 |
20 |
|
BMI (%) |
|
|
|
|
|
<18.50 |
8 |
8 |
0 |
0 |
|
18.50-24.99 |
84 |
84 |
100 |
96 |
|
25.00-29.99 |
8 |
4 |
0 |
0 |
0.286 |
30.00-34.99 |
0 |
4 |
0 |
0 |
|
35.00-39.99 |
0 |
0 |
0 |
4 |
|
≥40 |
0 |
0 |
0 |
0 |
|
Episiotomy (%) |
|
|
|
|
|
Given |
80 |
72 |
84 |
64 |
0.369 |
Not given |
20 |
28 |
16 |
36 |
|
Table-2:
Post-delivery data in four groups
|
Group
A Oxytocin |
Group
B Carboprost |
Group
C Methylergometrine |
Group
D Misoprostol |
p-value |
Duration of third stage of labor (minutes) |
4.72 |
3.84 |
5.04 |
4.93 |
0.002 |
Amount of blood loss (ml) |
223.2 |
131.8 |
435 |
255.8 |
<0.0001 |
Drop in hemoglobin (gm%) |
0.372 |
0.236 |
0.872 |
0.44 |
<0.0001 |
Number of patients having blood loss > 500 ml |
0 |
0 |
6 |
0 |
0.0004 |
Number of patients requiring blood transfusion |
0 |
0 |
2 |
0 |
0.111 |
Discussion
Postpartum hemorrhage is one of the most
important cause for maternal deaths throughout the world. Active management of
third stage of labor and the use of prophylactic oxytocics has reduced its
incidence in many countries. The primary aim in the management of postpartum
hemorrhage should be its prevention. The active management of the third stage
with routine prophylactic administration of oxytocics at the time of delivery
of the anterior shoulder of the fetus has been shown to reduce the risk of
postpartum hemorrhage by about 40% [5,10].
Recent studies show that there are still wide
variations in practice around the world in the management of third stage of
labour. Methyl ergometrine is a conventional oxytocic used extensively but is
associated with unpleasant side effects like hypertension. Intramuscular
oxytocin used alone has been found effective in preventing postpartum hemorrhage
with fewer side effects and is recommended by world health organization but
most of the times additional uterotonics are required [8,11]. Various drugs and
routes of administration have been tested with varying success. Oxytocin is
probably the most commonly used oxytocic and has been well known in midwifery
for a long time. Though commonly used it is not the potent drug and many a
times requires additional drugs and blood loss is more compared with other
drugs [11].
The production of PGF2α in the decidual
tissue was found to be more when obtained during labour indicating the increase
in the synthesis and release of PGF2α into the circulation. PGF 2α is a
powerful uterotonic agent with a physiological role in human parturition both
in the delivery of the foetus and control of post partum bleeding. The
discovery of prostaglandins and its analogues as an oxytocics has improved
prospect in modern era in control of PPH due to its significant influence on
uterine tone resulting in minimizing blood loss which outweighs its cost. The
side effects are also subtle [12-13]. Hence this study was conducted at Al
Ameen medical college to evaluate the four uterotonic drugs. This study has
shown that that carboprost is the uterotonic of choice followed by oxytocin for
active management of third stage of labor.
Table-3:
Mean duration of third stage
Study |
Methyl ergometrine |
Carboprost |
Oxytocin |
Misoprostol |
Singh nisha etal
[20] |
5.52 minutes |
6.10 minutes |
- |
|
Anjaneyu etal [13] |
6.1 minutes |
3.5 minutes |
-- |
|
Bhattacharya et
al [4] |
8.08 minutes |
4.8 minutes |
- |
|
B. Rajupuroshotam
etal [19] |
3.6 minutes |
2.63 minutes |
- |
|
Present study |
5.04 minutes |
3.84 minutes |
4.72 minutes |
4.93 minutes |
There are few studies where carboprost has
been compared with methyl ergometrine and found that the mean duration of third
of labour with carboprost was comparable to our study [14,15]. As compared to
other studies and in accordance with it, the present study showed decrease in
mean duration of third stage of labor incarboprost group was 3.84 minutes
compared to oxytocin 4.72 minutes. Therefore carboprost can be effective in
reducing the duration of third stage of labour.
Table-4:
Comparison of estimated blood loss in ml
Study |
Methyl ergometrine |
Carboprost |
Oxytocin |
Misoprostol |
Reddy et al [14] |
202 ml |
127ml |
- |
|
B. Rajupuroshotam
[19] |
169ml |
111ml |
- |
|
Present study |
435ml |
131.8ml |
223.2ml |
255.8ml |
Various studies have shown that the mean
blood loss with carboprost 125μg was less compared to methyl ergometrine. Few
studies compared carboprost with syntometrine, which did not show any
difference in mean blood loss in both the group [14]. In the present study mean
blood loss in third stage in carboprost was 131.8 ml and oxytocin was 223.2 ml.
(p value of 0.0001) which was highly significant [11]. None of them developed
PPH in carboprost group but 6 women had PPH in methylergometrine group. This
was comparable with other studies as shown in the table. Hence carboprost is
effective in reducing blood loss and carboprost has sustained impact on tone of
uterus. Hemoglobin was 0.3 in oxytocin and 0.23 carboprost, 0.87gm% in
methylergometrine group, 0.44gm% in misoprostol group which was statistically
significant (p value of 0.0001). Two required blood transfusion in
methylergometrine group and none in other 3 groups.
In group A, minor side effects in the form of
shivering, vomiting and headache were observed. Our findings are not consistent
with that of Gohil J et al (2011) as the incidence of these minor side effects
was much lowerintheir study [21].
In group B Diarrhea and vomiting were most
commonly observed inalong with chills in only 12%. This is comparable to the
study of Chua S et al (1995) where they found a significant increase in the
incidence of diarrhea with prostidin [24].
In group C in addition to shivering and
nausea, side effects like hypertension was also observed in 24% of patients,
study being consistent with that of Gohil J et al (2011) as patients exhibited
hypertension in their study also [21].
In group D, minor side effects, like
shivering and fever, were present in 48% and 56% of patients. Our study is
consistent with the study of El Refaey et al (1997), Hofmeyer G J et al (1998),
F Amant et al (1999), Hazem El- Rafaey et al (2000) in which their patients
also exhibited fever and shivering [22,23,25].
The only Drawback in using carboprost is its
storage in cold chain at 2- 4 celsius while oxytocin can be stored at room
temperature.
Conclusion
Carboprost when used prophylactically results
in minimal blood loss with fewer side effects. This small dose 125μg is well
tolerated by the patients. An added advantage is it can be used in patients
with hypertension and cardiovascular disease. In India where anemia highly
prevalent, the risk of PPH is very high. Intramuscular carboprost, a potent
uterotonic is a desirable drug as it is well tolerated in small doses and
significantly reduces the risk of PPH by limiting duration of 3rd
stage of labour & by reducing the blood loss Our study emphasizes that
carboprost is better alternative to intramuscular oxytocin in active management
of third stage of labour.
Acknowledgements- All
my regards to my patients without whom the study was not possible and the
ethical committee of Al Ameen medical college and my team in department of OBG.
Contribution by Co-Authors: Our corresponding author and second author are senior professor and
experienced in this field, hence their guidance helped us in selecting the type
of study in various discussions of cases and getting maximum number of study
material and patients.
What
this study adds to existing knowledge:
1. Our study proves that carboprost is most
effective and well tolerated uterotonic in prevention of PPH.
2. Lesser requirement of additional uterotonics
and blood transfusion.
Declarations
Funding: No
source of funding
Conflict of interest: None declared
Ethical approval:
The study was approved by the institutional ethics committee.
References
How to cite this article?
Patil A.S., Dandavate V, Thobbi V. A comparative study of oxytocin, carboprost, methylergometrine and misoprostol in prevention of postpartum haemorrhage a prospective study. Obg Rev: J obstet Gynecol 2019;5(2):99-105.doi:10. 17511/ jobg.2019.i2.03