期刊论文详细信息
BMC Pregnancy and Childbirth
Bemiparin versus enoxaparin as thromboprophylaxis following vaginal and abdominal deliveries: a prospective clinical trial
Namir G Al Tawil3  Mahabad S Ali1  Parez R Muhammad2  Rojan K Jawad2  Shahla K Alalaf2 
[1] Hawler Ministry of Health, Directorate of Health, Kurdistan Region, Erbil, Iraq;Department of Obstetrics and Gynaecology, College of Medicine, Hawler Medical University, Kurdistan Region, Erbil, Iraq;Department of Community Medicine, College of Medicine, Hawler Medical University, Kurdistan Region, Erbil, Iraq
关键词: Postpartum thromboprophylaxis;    Low-molecular-weight heparin;    Enoxaparin;    Bemiparin;   
Others  :  1161111
DOI  :  10.1186/s12884-015-0515-2
 received in 2014-11-12, accepted in 2015-03-23,  发布年份 2015
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【 摘 要 】

Background

Venous thromboembolism (VTE) is a leading cause of maternal mortality and morbidity, with the highest incidence occurring during the postpartum period. This study compared the ability of two types of low-molecular-weight heparin, enoxaparin and bemiparin, to decrease the incidence of VTE following elective caesarean section, emergency caesarean section, and vaginal delivery in women who had risk factors for thromboembolism.

Methods

In this prospective clinical trial using a sequential group allocation method, 7020 haemodynamically stable women delivered vaginally or abdominally at the Maternity Teaching Hospital, Kurdistan region, Erbil, Iraq, between May 1, 2012, and November 1, 2013. These women had risk factors for VTE and were allocated to the following groups: treatment with 3500 IU/day of bemiparin, 4000 IU/day of enoxaparin, or no intervention (control). The first dose was administered 6 hours after vaginal or abdominal delivery, or 8 hours after delivery in women receiving spinal anaesthesia. Subsequent doses were administered daily for up to 6 days. The incidence of VTE was assessed for up to 40 days postpartum. Data were analyzed using the Statistical Package for Social Sciences version 19. Proportions were compared using the chi square test of association or Fisher’s exact test. Binary logistic regression analysis was used with VTE as the dependent variable.

Results

VTE occurred in 1 (0.042%) woman in the bemiparin group, two (0.085%) women in the enoxaparin group, and nine (0.384%) women in the control group (P = 0.017). Regression analysis showed that women on bemiparin (OR = 0.106; 95% CI = 0.013–0.838) and enoxaparin (OR = 0.226; 95% CI = 0.049–1.049) were at lower risk of developing VTE than control women. Adverse events in the enoxaparin group included wound dehiscence, haematoma, and separation. None of these occurred in the bemiparin group.

Conclusions

Postpartum bemiparin is significantly effective as a prophylaxis for VTE. Wound complications develop after use of enoxaparin, but not after bemiparin.

Trial registration

ClinicalTrials.gov; Identifier: NCT01588171 webcite; date: April 26, 2012.

【 授权许可】

   
2015 Alalaf et al.; licensee BioMed Central.

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【 参考文献 】
  • [1]Rosendaal FR: Risk factors for venous thrombotic disease. Thromb Haemost 1999, 82:610-9.
  • [2]James AH, Tapson VF, Goldhaber SZ: Thrombosis during pregnancy and the postpartum period. Am J Obstet Gynecol 2005, 193:216-9.
  • [3]Wu P, Poole TC, Pickett JA, Bhat A, Lees CC: Current obstetric guidelines on thromboprophylaxis in the United Kingdom: evidence based medicine? Eur J Obstet Gynecol Reprod Biol 2013, 168:7-11.
  • [4]Bates SM, Greer IA, Pabinger I, Sofaer S, Hirsh J: American College of Chest Physicians: Venous thromboembolism, thrombophilia, antithrombotic therapy, and pregnancy: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines (8th Edition). Chest 2008, 133:844S-86.
  • [5]Bain E, Wilson A, Tooher R, Gates S, Davis LJ, Middleton P: Prophylaxis for venous thromboembolic disease in pregnancy and the early postnatal period. Cochrane Database Syst Rev 2014, 2:CD001689.
  • [6]Royal College of Obstetricians and Gynaecologists. Reducing the risk of thrombosis and embolism during pregnancy and the puerperium 2009 (Green-top Guideline; No. 37).
  • [7]Hill J, Treasure T: Reducing the risk of venous thromboembolism in patients admitted to hospital: summary of NICE guidance. BMJ 2010, 340:c95.
  • [8]Cosmi B, Palareti G: Old and new heparins. Thromb Res 2012, 129:388-91.
  • [9]Lucas DN, Yentis SM, Kinsella SM, et al.: Urgency of caesarean section: a new classification. J R Soc Med 2000, 93:346-50.
  • [10]Greer IA: Thrombosis in pregnancy: maternal and fetal issues. Lancet 1999, 353:1258-65.
  • [11]Dizon-Townson DS, Nelson LM, Jang H, Varner MW, Ward K: The incidence of the factor V Leiden mutation in an obstetric population and its relationship to deep vein thrombosis. Am J Obstet Gynecol 1997, 176:883-6.
  • [12]Greer IA, Nelson-Piercy C: Low-molecular-weight heparins for thromboprophylaxis and treatment of venous thromboembolism in pregnancy: a systematic review of safety and efficacy. Blood 2005, 106:401-7.
  • [13]Piazza G, Goldhaber SZ: Acute pulmonary embolism: part II: treatment and prophylaxis. Circulation 2006, 114:e42-7.
  • [14]Heit JA, Silverstein MD, Mohr DN, Petterson TM, O’Fallon WM, Melton LJ 3rd: Predictors of survival after deep vein thrombosis and pulmonary embolism: a population-based, cohort study. Arch Intern Med 1999, 159:445-53.
  • [15]Ferres MA, Olivarez SA, Trinh V, Davidson C, Sangi-Haghpeykar H, Aagaard-Tillery KM: Rate of wound complications with enoxaparin use among women at high risk for postpartum thrombosis. Obstet Gynecol 2011, 117:119-24.
  • [16]Tooher R, Gates S, Dowswell T, Davis LJ: Prophylaxis for venous thromboembolic disease in pregnancy and the early postnatal period. Cochrane Database Syst Rev 2010, 5:CD001689.
  • [17]Connolly T: Thromboembolism prophylaxis and cesarean section: a survey of general obstetricians. South Med J 2003, 96:146-8.
  • [18]Orme ML, Lewis PJ, de Swiet M, et al.: NICE 2004 National Collaborating Centre for Women’s and Children’s Health, Commissioned by NICE. Caesarean section. RCOG Press, London; 2004.
  • [19]Cruz M, Fernández-Alonso AM, Rodríguez I, et al.: Postcesarean thromboprophylaxis with two different regimens of bemiparin. Obstet Gynecol Int 2011, 2011:548327.
  • [20]Blondon M, Perrier A, Nendaz M, Righini M, et al.: Thromboprophylaxis with low-molecular-weight heparin after cesarean delivery. Thromb Haemost 2010, 103:129-37.
  • [21]Segal S, Sadovsky E, Weinsten D, Polishk WZ: Prevention of postpartum venous thrombosis with low doses of heparin. Eur J Obstet Gynecol Reprod Biol 1975, 5:273-6.
  • [22]O’Connor DJ, Scher LA, Gargiulo NJ 3rd, Jang J, Suggs WD, Lipsitz EC: Incidence and characteristics of venous thromboembolic disease during pregnancy and the postnatal period: acontemporary series. Ann Vasc Surg 2011, 25:9-14.
  • [23]Heit JA, Kobbervig CE, James AH, Petterson TM, Bailey KR, Melton LJ 3rd: Trends in the incidence of venous thromboembolism during pregnancy or postpartum: a 30-year population-based study. Ann Intern Med 2005, 143:697-706.
  • [24]Barbour LA, Pickard J: Controversies in thromboembolic disease during pregnancy: a critical review. Obstet Gynecol 1995, 86:621-33.
  • [25]Rutherford S, Montoro M, McGehee W, Strong T: Thromboembolic disease associated with pregnancy: An 11-year review. Am J Obstet Gynecol 1991, 164:286. [abstract]
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