|
|
| |
| ORIGINAL ARTICLES |
| |
| Disseminated intravascular coagulation and massive obstetric hemorrhage. Management dilemma |
| |
| Lulu A. Al-Nuaim, Mohamed S. Mustafa, Abdel Galil M. Abdel Gader
|
| |
| ABSTRACT |
| |
Objectives: The objective of this retrospective study is to reflect on our experience on an optimal management for major postpartum hemorrhage, which would prevent the occurrence and complications of disseminated intravascular coagulation and minimize maternal mortality and morbidity.
Methods: Ten cases out of the 30,000 of total deliveries of severe obstetric hemorrhage associated with disseminated intravascular coagulation were studied. This study was carried out over a 7 year period, October 1988 through to September 1995, at the Obstetric Unit, King Khalid University Teaching Hospital, Riyadh, Kingdom of Saudi Arabia.
Results: All of the 10 women received packed red blood cells, 8 had fresh frozen plasma, and 6 received platelet transfusion. The 10 cases developed disseminated intravascular coagulation following medical and surgical management, all women needed hysterectomy, 4 subtotal, 6 total, and 5 women had relaparotomy and pelvic packing. Two had bladder injuries. There was no maternal death.
Conclusions: An early resort to hysterectomy when conservative measures fail, will minimize maternal morbidity and mortality. In case of continuous bleeding after hysterectomy, pelvic packing proved to be effective.
|
| |
| |
| Saudi Medical Journal 2002; Vol. 23 (6): 658-662 |
| |
|
| |
Severe postpartum hemorrhage (PPH) is defined as blood loss of more than 1000 ml. Since blood loss after delivery of the baby is difficult to measure accurately, major PPH may best be defined by a fall in hematocrit (Hct) or by the need for blood transfusion.1 Postpartum hemorrhage accounts for 28% of maternal deaths in developing countries, around 125,000 deaths each year, as there are 125,000,000 births annually in the developing world, the risk of maternal death from PPH is approximately one in 1000 deliveries.2-4 In the Kingdom of Saudi Arabia (KSA), PPH accounts for 20% of direct maternal deaths. Hemorrhage is the 4th leading cause of death in the United Kingdom. Eight deaths out of the 15 hemorrhage deaths were attributed directly to PPH alone and the risk of death from obstetric hemorrhage is 1:100,000 deliveries.5 The present report concerns 10 cases of major obstetric hemorrhage with disseminated intravascular coagulation (DIC), as evidenced by low platelet count prolongation of the coagulation screening tests, low fibrinogen level, and the presence of fibrin degradation product (FDP). The management in the face of a life-threatening obstetric hemorrhage with DIC, unfortunately, is not always evidence-based. When faced with such an emergency, obstetricians tend to give whatever is available at hand hoping to save the life of the mother. The aim of this retrospective study is to reflect on our experience on an optimal and cost-effective management protocol, which would prevent the occurrence and complications of DIC and minimize maternal mortality and morbidity.
Methods. Ten cases of severe obstetric hemorrhage that progressed to DIC were studied retrospectively over a 7 year period, October 1988 through to September 1995, in the Obstetric Unit, King Khalid University Teaching Hospital, Riyadh, KSA. Information was retrieved from the medical records regarding age and parity, detailed obstetric history illustrating the number of previous lower segment cesarian section (LSCS), placental localization, mode of delivery, blood loss, and clinical and laboratory evidence of disseminated intravascular coagulation (DIC). The available pre-hemorrhage, intra-hemorrhage, and post-replacement laboratory parameters were recorded. Replacement therapy in the form of crystalloid, colloid, blood and various blood components (platelets, fresh frozen plasma, and cryoprecipitate) was used. Conservative medical therapy includes various oxytoxic drugs, ranging from ergometrine, oxytocin and prostaglandin, administered via different routes. The antifibrinolytic agent tranexamic acid was used in some patients. Conservative surgical measures used in this study included uterine massage, suturing of placental bed, uterine packing, uterine and internal iliac artery ligation. Hysterectomy, total or subtotal was resorted to when conservative surgical attempts were not successful.
Results. Out of the 30,000 total deliveries during the 7 years study period, 735 patients developed postpartum hemorrhage of more than 500 ml blood loss giving an incidence of 2.5%. Severe postpartum hemorrhage of more than 1000 ml blood loss occurred in 84 patients giving an incidence of 0.5%. Ten cases of the severe PPH progressed to DIC giving an incidence of 0.03%. The age of the 10 patients ranged between 25 years - 40 years (mean = 36.1 years); nine patients were 35 years and above. Four patients were of high parity (6 and above), 4 were para 3, and 2 were para 2+0. Six patients had repeat LSCS for all their previous deliveries, and 3 patients had one previous cesarean section. The patient who did not have previous cesarean section had spontaneous vertex delivery at 30 weeks gestation, fo |
| |
|
| From the Department Obstetrics & Gynecology, (Al-Nuaim, Mustafa) and Blood Bank, (Gader), College of Medicine and King Khalid University Hospital, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Received 21st November 2001. Accepted for publication in final form 27th January 2002.
Address correspondence and reprint request to: Dr. Mohamed S. Mustafa, Department of Obstetrics & Gynecology (36), King Khalid University Hospital, PO Box 7805, Riyadh 11472, Kingdom of Saudi Arabia. Fax. +966 (1) 4620095.
|
| |
|
|
| References |
1. Joupilla P. Postpartum hemorrhage. Curr Opin Obstet Gynecol 1995; 7: 446-450.
2. Chamberlain GVP. The clinical aspects of massive hemorrhage. In: Patel N, editor. Maternal mortality - The way forward. London, (United Kingdom): RCOG; 1992. p. 54-62.
3. Abou Zahr C, Roystan E. Maternal mortality: Global factbook. Geneva: World Health Organization, 1991.
4. Edwards GM. Britannica Book. Chicago, (IL): Encyclopedia Britannica; 1996. p. 279.
5. Department of Health Report on confidential inquiries into maternal deaths in the UK 1991-1993. London (United Kingdom): HMSO; 1996. p. 32-47.
6. Stones RW, Paterson CM, Sauders NSG. Risk factors for major obstetric hemorrhage. European Journal of Obstetrics, Gynecology, and Reproductive Biology 1993; 48: 15-18.
7. Tsu VD. Post-hemorrhage in Zimbabwe: a risk factor analysis. Br J Obstet Gynecol 1993; 100: 327-333.
8. Hayashi RH. The role of prostaglandin in the treatment of postpartum hemorrhage. J Obstet Gynaecol 1990; 19 (Suppl 2): 21-24.
9. Ghorab S, Al-Nuaim L, Al-Jabari A, Al-Meshari A, Mustafa MS, Abotalib Z et al. Abdomino-pelvic packing to control severe haemorrhage following hysterectomy. J Obstet Gynaecol 1999; 19: 155-158.
10. Fernandez H, Pons JC, Chambon G, Frydman R, Papievnik E. Internal iliac artery ligation in postpartum hemorrhage. European Journal of Obstetrics, Gynecology, and Reproductive Biology 1998; 28: 213-220.
11. Pelage JP, LepDref O, Jacob D, Soyer P, Herbretea D, Rymer R. Selective arterial embolisation of the uterine arteries in the management of intractable postpartum hemorrhage. Acta Obstet Gynecol Scand 1999; 78: 698-703.
12. Hori A, Nagata Y, Shimabukuro K, Ohshiro K, Hanashiro Y, Miyazaki T et al. Transcatheter arterial embolisation for postpartum hemorrhage. Rinsho Hoshasen 1990; 35: 645-647.
13. Levi M, de Jonge E, Van der Poll T. Ten Cate H-Novel approaches to the management of disseminated intravascular coagulation (review) Crit Care Med 2000; 28 (9 Suppl): 20-24.
14. Kobayashi T, Terao T, Maki Masahiro, Ikenoue T. Diagnosis and management of acute obstetrical DIC. Semin Throm Hemost 2001; 27: 161-167.
15. Riewald M, Riess H. Treatment options for clinically disseminated intravasular coagulation. Semin Throm Hemost 1998; 24: 53-59.
16. Maruyama I. Recombinant thrombomodulin and activated protein C in the treatment of disseminated intravascular coagulation. Thromb Haemost 1999; 82: 718-721.
|
|
|
|