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DOI: 10.1111/j.1471-0528.2011.02954.x
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risk factors.
Introduction
Excess postpartum haemorrhage is a serious complication
of delivery and a major cause of maternal morbidity and
mortality worldwide.1 To prevent the condition from
occurring, and to provide prompt and accurate treatment,
knowledge of risk factors for excess postpartum haemorrhage is essential.2,3 Previous research suggests that parity,
high offspring birthweight, labour dystocia and caesarean
section are factors that may increase the risk of excess
haemorrhage.49 In addition, complications that are closely
linked to the placenta, including placenta praevia, placental
abruption, as well as a retained placenta and pre-eclampsia,
have been related to excess postpartum haemorrhage.3,610
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2011 The Authors BJOG An International Journal of Obstetrics and Gynaecology 2011 RCOG
Methods
Study population
In Norway, a total of 332 705 deliveries occurred after
16 weeks of gestation from 1999 through 2004. We
restricted the analyses to singleton deliveries occurring after
21 weeks of gestation, leaving 308 717 deliveries eligible for
the study. Data were obtained from the Medical Birth Registry of Norway, which has been in operation since 1967.12
Deliveries after 16 weeks of gestation are compulsorily notified to the registry on standardised forms that are filled in
by the midwife or doctor in charge of the delivery. Since
1999, placental weight has been included in the registration
to the Medical Birth Registry. A large proportion of pregnancies with delivery between 16 and 21 weeks of gestation
had no information available on placental weight. Therefore, we only included pregnancies with delivery after the
21 weeks of gestation.
Study factors
Excess postpartum haemorrhage at delivery is recorded in
the Medical Birth Registry in two separate categories, as
either 500 ml, or as 1500 ml, within 2 hours after delivery. The blood volume is visually estimated by the midwife
or doctor in charge of the delivery. In this study, we defined
500 ml as excess postpartum haemorrhage. However, we
also present the crude prevalence of postpartum haemorrhage 1500 ml related to placental weight. Placental weight
is recorded in grams, and divided into six categories in the
analyses: <300, 300499, 500699, 700899, 9001099 and
1100 g or higher, using the group of 300499 g as the reference. We also constructed a ratio of placental weight and
birthweight by dividing placental weight (g) by birthweight
(g). In the analyses, the ratio was divided into six categories:
<0.14, 0.150.19, 0.200.24, 0.250.29, 0.300.34, or 0.35.
Hence, a relatively high ratio will indicate a large placenta
relative to offspring birthweight.
We also studied the associations of placental weight and
placental/birthweight ratio with postpartum haemorrhage
after adjustment for pregnancy complications that are
strongly related to the placenta and to excess postpartum
haemorrhage. Hence, information on placenta praevia, placental abruption and retained placenta (manual/operative
delivery of the placenta) were included in the analyses as
potentially confounding factors. Other variables that were
taken into account, included parity (coded: 1, 2 or 3 previous deliveries), caesarean section (yes or no), pre-eclampsia (blood pressure >140/90 mmHg and proteinuria, yes or
no), labour dystocia (duration of labour >12 hours after a
cervix opening of 4 cm, yes or no), perineal rupture (yes
Statistical analyses
We estimated the prevalence of excess postpartum haemorrhage (500 and 1500 ml) according to categories of placental weight, and we also estimated the prevalence of
postpartum haemorrhage (>500 ml) according to categories
of the placental weight to birthweight ratio. We used logistic
regression analysis to estimate odds ratios of excess postpartum haemorrhage (500 ml) according to placental weight
and the placental weight to birthweight ratio, and used 95%
CI to indicate precision of the estimates. We estimated both
crude and adjusted odds ratios, where adjustments were
made for birthweight in addition to placenta-related complications and complications related to delivery, as specified
above. The statistical analyses were performed by applying
SPSS version 17.0 (Chicago, IL, USA).
Ethics
The study was approved by the internal review board of
the Medical Birth Registry of Norway, and by the Norwegian Directorate of Health. All data in the study were
anonymous.
Results
Of all women in our study, 13.9% (42 813/308 717) had
postpartum haemorrhage 500 ml, and 1.4% (4306/
308 717) had postpartum haemorrhage 1500 ml. There
was a gradual increase in the prevalence of excess postpartum haemorrhage (500 and 1500 ml) with increasing
placental weight, except for the lowest category of placental
weight (Figure 1). On average, 28.5% of women with placental weight 1100 g had postpartum haemorrhage
500 ml, compared with 11.5% among women with
placental weight between 300 and 499 g (reference). From
the reference category, the prevalence displayed a gradual
30
>500 ml
25
Percent
>1500 ml
20
15
10
5
0
<300
300 to
<500
500 to
<700
700 to
<900
900 to
<1100
>1100
2011 The Authors BJOG An International Journal of Obstetrics and Gynaecology 2011 RCOG
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Eskild, Vatten
Table 1. Crude and adjusted odd ratios (OR) with 95% confidence intervals (95% CI) for postpartum haemorrhage of more than 500 ml,
according to placental weight and other selected pregnancy factors
Women with PPH/Total (%)
Total
Placental weight (g)
<300
300499
500699
700799
8001099
1100
Placental complications
Placenta praevia*
Placental abruption*
Retained placenta*
Parity
0
1
2
3
Caesarean section*
Pre-eclampsia*
Labour dystocia*
Perineal rupture*
Birthweight (g)
<1500
15002999
30004499
4500
Crude OR
95% CI
Adjusted OR
95% CI
1.75
1.0 Ref
0.96
1.44
2.19
3. 05
1.522.01
0.771.09
0.941.02
1.391.50
2.092.30
2.803.32
0.95
1.0 Ref
1.14
1.59
2.10
2.54
1.091.20
1.511.67
1.982.23
2.312.79
8.41
6.18
8.66
7.309.69
5.546.89
8.239.12
4.64
3.69
6.71
4.005.39
3.284.15
6.357.09
(16.4)
(12.3)
(11.3)
(11.1)
1.0 ref
0.72
0.65
0.64
0.700.74
0.630.67
0.616.75
1.0 ref
0.77
0.69
0.67
0.750.79
0.660.71
0.640.71
002
386
859
769
(32.6)
(21.7)
(28.7)
(22.7)
3.98
1.76
2.75
1.87
3.894.07
1.691.84
2.662.85
1.791.96
3.19
1.33
1.64
2.02
3.113.27
1.271.40
1.581.70
1.922.12
538/2407
4479/37 103
34 110/254 424
3686/14 783
(22.4)
(12.1)
(13.4)
(24.9)
1.0 ref
0.48
0.54
1.15
0.430.53
0.490.59
1.041.28
1.0 ref
0.74
0.92
1.37
0.650.85
0.801.05
1.191.58
(18.6%)
(11.5)
(11.3)
(15.8)
(22.3)
(28.5)
452/789 (57.3)
644/1300 (49.5)
3516/6234 (56.4)
22 096/135 093
13 442/108 850
5464/48 517
1811/16 257
14 021/29
2682/12
5989/20
2444/10
All singleton pregnancies in Norway from 1999 through 2004 (n = 308 717).
*Compared to women without the condition.
PPH, postpartum haemorrhage.
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2011 The Authors BJOG An International Journal of Obstetrics and Gynaecology 2011 RCOG
Discussion
In this large population study, there was a positive association
of placental weight with excess postpartum haemorrhage.
Table 2. Crude and adjusted odds ratios (OR) with 95% confidence intervals (95% CI) for postpartum haemorrhage of more than 500 ml
according to the ratio of placental weight and birth weight (in grams). A high ratio indicates a large placental weigh relative to birth weight.
All singleton pregnancies in Norway from 1999 through 2004 (n = 308 717)
Placental weight/birthweight
Total
<0.15
0.15 to
0.20 to
0.25 to
0.30 to
0.35
<0.20
<0.25
<0.30
<0.35
(13.9)
(12.6)
(12.5)
(15.9)
(20.9)
(23.2)
(23.0)
Crude OR
95% CI
Adjusted OR*
95% CI
1.0 ref
0.99
1.31
1.84
2.09
2.07
0.951.03
1.261.36
1.741.94
1.852.35
1.802.39
1.0 ref
1.00
1.18
1.45
1.32
1.40
0.961.04
1.141.23
1.361.53
1.171.50
1.201.63
*Adjustment was made for placenta praevia, placental abruption, retained placenta, parity, caesarean section, pre-eclampsia, labour dystocia and
perineal rupture.
PPH, postpartum haemorrhage.
2011 The Authors BJOG An International Journal of Obstetrics and Gynaecology 2011 RCOG
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Eskild, Vatten
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Disclosure of interest
There is no conflict of interest related to this work.
Contribution to authorship
AE conceived the idea, analysed and interpreted the data
and wrote the paper. LJV interpreted the data and wrote
the paper.
Funding
The study was financially supported by Akershus University
Hospital and by the Norwegian University of Science and
Technology.
Acknowledgements
We are indebted to the women who provided the information that enabled this study. j
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