Research Article | | Peer-Reviewed

Near-Miss Maternal Mortality: Survival After Massive Postpartum Hemorrhage, Disseminated Intravascular Coagulopathy, and Multiorgan Failure

Received: 16 March 2026     Accepted: 13 April 2026     Published: 24 August 2026
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Abstract

Background: Postpartum hemorrhage (PPH) is a leading cause of maternal morbidity and mortality worldwide. Primary PPH, occurring within the first 24 hours after delivery, is the most common form and may rapidly progress to disseminated intravascular coagulation (DIC), multiorgan failure, and maternal near-miss events if bleeding is not promptly controlled. Patients with underlying thrombophilia are at increased risk for severe hemorrhage and coagulopathy. Case Presentation: A 35-year-old gravida 8, para 4, aborta 3 woman with Factor V Leiden thrombophilia presented for elective induction of labor at 38+4 weeks. Antenatal care was suboptimal. She initially underwent vaginal delivery but was converted to Cesarean section due to labor complications. Immediately postpartum, she developed severe PPH secondary to uterine atony, unresponsive to uterotonics and balloon tamponade. Total abdominal hysterectomy was performed, but hemorrhage persisted. Interventions: Surgical re-exploration identified bleeding from the left infundibulopelvic ligament. Hemostasis was achieved via bilateral internal iliac artery ligation and left oophorectomy. The patient received approximately 60 units of blood products, including packed RBCs, platelets, and fresh frozen plasma. She required ICU admission for disseminated intravascular coagulation (DIC), multiorgan failure, vasopressor support (norepinephrine and vasopressin), mechanical ventilation, and empirical broad-spectrum antibiotics. Outcome: The patient gradually improved, with hemodynamic stabilization, resolution of DIC, and normalization of renal and hepatic function. She was discharged in stable condition on postpartum day 11. Conclusion: This case demonstrates that hysterectomy may not always control catastrophic PPH. Early recognition of alternative bleeding sources, aggressive resuscitation, and multidisciplinary critical care are essential, especially in high-risk patients with thrombophilia, to improve survival in patients with refractory primary postpartum hemorrhage.

Published in Journal of Gynecology and Obstetrics (Volume 14, Issue 4)
DOI 10.11648/j.jgo.20261404.12
Page(s) 97-100
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2026. Published by Science Publishing Group

Keywords

Postpartum Hemorrhage, Disseminated Intravascular Coagulation, Multiorgan Failure, Thrombophilia, Case Report

1. Introduction
Postpartum hemorrhage (PPH) is defined by the American College of Obstetricians and Gynecologists (2017) as blood loss exceeding 500 mL after vaginal delivery or 1000 mL after Cesarean section within 24 hours, with clinical signs of hypovolemia regardless of delivery mode , 3]. PPH can be classified as primary (within 24 hours of delivery) or secondary (occurring after 24 hours up to 12 weeks postpartum) . The most common cause of PPH is uterine atony, although trauma, retained tissue, and coagulopathies may also contribute , 4]. Globally, approximately 3% of deliveries are complicated by PPH, which remains a leading cause of maternal morbidity and mortality, accounting for nearly 25% of pregnancy-related deaths, especially in low- and middle-income countries .
Management of PPH requires a multidisciplinary approach, including assessment of blood loss, fluid resuscitation, correction of coagulopathy, and source control. Stepwise interventions range from uterotonics and mechanical measures to surgical procedures, with hysterectomy considered a last-resort life-saving option if other measures fail , 6]. Prophylactic strategies include active management of the third stage of labor and early identification of high-risk patients, including those with thrombophilia, prior PPH, or other coagulopathies.
This case was selected for reporting due to its rarity and clinical significance: despite stepwise management culminating in hysterectomy, the patient continued to bleed due to occult retroperitoneal hemorrhage, compounded by underlying thrombophilia, developed disseminated intravascular coagulation (DIC), and progressed to multiorgan failure requiring intensive care. It highlights the importance of early recognition of alternative bleeding sources, aggressive resuscitation, and multidisciplinary critical care in high-risk patients.
2. Case Presentation
A 35-year-old gravida 8, para 4, aborta 3 woman presented at 38+4 weeks of gestation for elective induction of labor. Her obstetric history was significant for recurrent pregnancy loss associated with thrombophilia (Factor V Leiden). She was treated with low molecular weight heparin during the first four months of the current pregnancy and continued on daily aspirin. Antenatal care was suboptimal, with no glucose challenge test or detailed ultrasound performed.
Her previous obstetric history included four spontaneous vaginal deliveries complicated by PPH that did not require transfusions, and one dilation and curettage (D&C). She has a penicillin allergy. Family history was unremarkable.
The patient was initially planned for vaginal delivery; however, due to labor complications, an emergency cesarean section was performed, resulting in delivery of a healthy male infant. Immediately postpartum, she developed severe PPH secondary to uterine atony . Initial medical management with uterotonics and a Bakri balloon failed to control the hemorrhage, and she became hemodynamically unstable, necessitating multiple blood transfusions. Persistent hemorrhage prompted total abdominal hysterectomy, during which a small retroperitoneal hematoma was identified in the left cardinal ligament.
On the first postoperative day, intra-abdominal bleeding had persisted, and she required another surgical exploration, and approximately 2000 mL of clotted blood was evacuated. Active bleeding was found to arise from the left infundibulopelvic (suspensory) ligament. Hemostasis was achieved via bilateral internal iliac artery ligation, and left oophorectomy was performed as well. She received 3 units of fresh frozen plasma, 3 units of platelets, and 2 units of packed red blood cells (RBCs) during this surgery.
At intensive care unit admission (ICU), she developed disseminated intravascular coagulation (DIC), with multiorgan failure affecting renal (creatinine = 4.5 mg/dL), hepatic (aspartate transaminase (AST) = 1240 U/L, alanine transaminase (ALT) = 836 U/L), respiratory, and hematologic (platelet count dropping to 35,000/µL) systems. She experienced transfusion-related acute lung injury (TRALI), requiring oxygen therapy and mechanical ventilation. Additionally, high doses of vasopressin and norepinephrine were administered. About 60 units of blood products were given. Additionally, empirical broad-spectrum antibiotics, including metronidazole, vancomycin, and meropenem, were administered. The patient gradually improved, and was discharged on postpartum day 11 with normalization of lab tests and symptomatology.
3. Discussion
Postpartum hemorrhage (PPH) is defined as an estimated blood loss of over 500 mL after a vaginal delivery or an estimated blood loss of over 1,000 mL after a cesarean delivery , 7]. It remains a leading cause of maternal morbidity and mortality worldwide, particularly in low- and middle-income countries , 10]. This case report presents an unusual and severe case of refractory primary postpartum hemorrhage complicated by persistent retroperitoneal bleeding, disseminated intravascular coagulation, multiorgan failure and massive transfusion, illustrating the complexity of managing high-risk postpartum hemorrhage .
Uterine atony is the leading cause of PPH; it is estimated to contribute to about 70 to 80% of cases of PPH , regardless of the mode of delivery. Consequently, a stepwise approach to management is established, beginning with bimanual uterine massage and administration of uterotonic agents such as oxytocin, followed by second-line agents including methylergonovine or prostaglandins in cases of persistent bleeding. When medical therapy fails, mechanical and surgical alternatives are considered, including uterine balloon tamponade and uterine compression suture techniques such as B-Lynch as fertility-preserving options. In refractory cases, more invasive procedures such as uterine artery ligation or hysterectomy may be required as life-saving measures .
In this case, the hemorrhage persisted despite the stepwise approach to its management, which included uterotonic agents, balloon tamponade, and finally hysterectomy. This emphasizes that hysterectomy, although considered a definitive life-saving intervention, may fail to control bleeding when it originates from extra-uterine sources . Re-exploration identified active bleeding from retroperitoneal vessels and the left infundibulopelvic ligament, highlighting the presence of occult retroperitoneal hemorrhage that was not initially apparent. This underscores the need to maintain a high index of suspicion for alternative bleeding sources in cases of uncontrolled hemorrhage despite conventional management strategies. Definitive control of bleeding was finally attained through ligation of the bilateral internal iliac arteries and left oophorectomy, reinforcing the need to pursue aggressive surgical interventions when first-line measures are ineffective .
In our patient, the underlying thrombophilic condition further contributed to the complexity of the clinical course. Although thrombophilia is typically associated with a prothrombotic state, it may paradoxically predispose to consumptive coagulopathy in the setting of massive hemorrhage. This interplay between thrombosis and bleeding likely exacerbated the severity of DIC and contributed to persistent hemorrhage despite standard interventions .
In the patient’s case, DIC was most likely triggered by massive blood loss, compounded by tissue hypoperfusion and underlying thrombophilia, leading to widespread activation of the coagulation cascade with subsequent consumption of clotting factors and platelets, resulting in coagulopathy-driven hemorrhage. This is further evidenced by the results of the blood studies, which reflected ongoing consumptive coagulopathy requiring prompt correction with blood transfusion products, including fresh frozen plasma, platelets, and cryoprecipitates .
Massive transfusion in itself carries the risks of TRALI, hypocalcemia, hypothermia, and dilutional coagulopathy , all of which contributed to the clinical complexity of the patient. The development of multiorgan failure (renal, hepatic, respiratory) was a direct consequence of both hypoperfusion and DIC-induced microthrombi formation.
Our patient was admitted to the intensive care unit (ICU) for hemodynamic support, vasopressor treatment, and ventilatory support, which was critical for patient survival. The cumulative effect of vasopressin, noradrenaline, and empirical broad-spectrum antibiotics prevented secondary sepsis and further organ dysfunction. Recovery of renal and hepatic function in 11 days suggests successful critical care and gradual resolution of DIC. The case supports previous reports that early multidisciplinary critical care intervention improves survival in even near-miss maternal cases .
This case highlights several important clinical considerations: hysterectomy is not always definitive in controlling PPH; occult retroperitoneal bleeding should be considered in refractory cases; early correction of coagulopathy is essential; and the interaction between hemorrhage, thrombophilia, and DIC significantly complicates management.
This case has several limitations. As a single case report, the findings may not be generalizable. The precise contribution of the underlying thrombophilic condition to the development of DIC cannot be determined. Furthermore, it is possible that the lack of advanced coagulation monitoring may have limited the ability to provide more targeted hemostatic therapy.
4. Conclusion
This case highlights key clinical lessons in the management of severe PPH:
1) Consider alternative bleeding sources beyond the uterus when hemorrhage persists despite standard interventions.
2) Early recognition and prompt management of DIC are essential to prevent progression to multiorgan failure.
3) Multidisciplinary critical care involvement significantly improves survival in near-miss maternal cases.
Abbreviations

ALT

Alanine Aminotransferase

AST

Aspartate Aminotransferase

CS

Cesarean Section

D&C

Dilation and Curettage

ICU

Intensive Care Unit

PPH

Postpartum Hemorrhage

RBC

Red Blood Cells

TRALI

Transfusion-Related Acute Lung Injury

Author Contributions
Ibrahim Kattoush: Conceptualization, Data curation, Investigation; Resources, Writing – original draft
Haya Ewidat: Writing – original draft; Writing –review & editing, Validation
Ayat Fararjeh: Writing – original draft
Malak Hamdan: Writing – original draft
Khawlla Ghraeb: Writing – original draft
Mohammed Alra’e: Supervision, Validation, Project administration
Mohammad Saya’Reh: Writing – review & editing
Montaser Shrouf: Supervision, Resources
Conflicts of Interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
References
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[2] Neal S, Mahendra S, Bose K, Camacho AV, Mathai M, Nove A, et al. The causes of maternal mortality in adolescents in low and middle income countries: a systematic review of the literature. BMC Pregnancy Childbirth. 2016 Nov 11; 16(1): 352.
[3] Committee on Practice Bulletins-Obstetrics. Practice Bulletin No. 183: Postpartum Hemorrhage. Obstetrics and gynecology. 2017 Oct; 130(4): e168–86.
[4] Kerr RS, Weeks AD. Postpartum haemorrhage: a single definition is no longer enough. BJOG. 2017 Apr; 124(5): 723–6.
[5] Federspiel JJ, Eke AC, Eppes CS. Postpartum hemorrhage protocols and benchmarks: improving care through standardization. Am J Obstet Gynecol MFM. 2023 Feb; 5(2S): 100740.
[6] Bienstock JL, Eke AC, Hueppchen NA. Postpartum Hemorrhage. N Engl J Med. 2021 Apr 29; 384(17): 1635–45.
[7] Dahlke JD, Mendez-Figueroa H, Maggio L, Hauspurg AK, Sperling JD, Chauhan SP, et al. Prevention and management of postpartum hemorrhage: a comparison of 4 national guidelines. Am J Obstet Gynecol. 2015 Jul; 213(1): 76. e1-76. e10.
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[14] Gillissen A, van den Akker T, Caram-Deelder C, Henriquez DDCA, Bloemenkamp KWM, de Maat MPM, et al. Coagulation parameters during the course of severe postpartum hemorrhage: a nationwide retrospective cohort study. Blood Adv. 2018 Oct 9; 2(19): 2433–42.
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Cite This Article
  • APA Style

    Kattoush, I., Ewidat, H., Fararjeh, A., Hamdan, M., Ghraeb, K., et al. (2026). Near-Miss Maternal Mortality: Survival After Massive Postpartum Hemorrhage, Disseminated Intravascular Coagulopathy, and Multiorgan Failure. Journal of Gynecology and Obstetrics, 14(4), 97-100. https://doi.org/10.11648/j.jgo.20261404.12

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    ACS Style

    Kattoush, I.; Ewidat, H.; Fararjeh, A.; Hamdan, M.; Ghraeb, K., et al. Near-Miss Maternal Mortality: Survival After Massive Postpartum Hemorrhage, Disseminated Intravascular Coagulopathy, and Multiorgan Failure. J. Gynecol. Obstet. 2026, 14(4), 97-100. doi: 10.11648/j.jgo.20261404.12

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    AMA Style

    Kattoush I, Ewidat H, Fararjeh A, Hamdan M, Ghraeb K, et al. Near-Miss Maternal Mortality: Survival After Massive Postpartum Hemorrhage, Disseminated Intravascular Coagulopathy, and Multiorgan Failure. J Gynecol Obstet. 2026;14(4):97-100. doi: 10.11648/j.jgo.20261404.12

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  • @article{10.11648/j.jgo.20261404.12,
      author = {Ibrahim Kattoush and Haya Ewidat and Ayat Fararjeh and Malak Hamdan and Khawlla Ghraeb and Mohammed Alra’e and Mohammad Saya’Reh and Montaser Shrouf},
      title = {Near-Miss Maternal Mortality: Survival After Massive Postpartum Hemorrhage, Disseminated Intravascular Coagulopathy, and Multiorgan Failure},
      journal = {Journal of Gynecology and Obstetrics},
      volume = {14},
      number = {4},
      pages = {97-100},
      doi = {10.11648/j.jgo.20261404.12},
      url = {https://doi.org/10.11648/j.jgo.20261404.12},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.jgo.20261404.12},
      abstract = {Background: Postpartum hemorrhage (PPH) is a leading cause of maternal morbidity and mortality worldwide. Primary PPH, occurring within the first 24 hours after delivery, is the most common form and may rapidly progress to disseminated intravascular coagulation (DIC), multiorgan failure, and maternal near-miss events if bleeding is not promptly controlled. Patients with underlying thrombophilia are at increased risk for severe hemorrhage and coagulopathy. Case Presentation: A 35-year-old gravida 8, para 4, aborta 3 woman with Factor V Leiden thrombophilia presented for elective induction of labor at 38+4 weeks. Antenatal care was suboptimal. She initially underwent vaginal delivery but was converted to Cesarean section due to labor complications. Immediately postpartum, she developed severe PPH secondary to uterine atony, unresponsive to uterotonics and balloon tamponade. Total abdominal hysterectomy was performed, but hemorrhage persisted. Interventions: Surgical re-exploration identified bleeding from the left infundibulopelvic ligament. Hemostasis was achieved via bilateral internal iliac artery ligation and left oophorectomy. The patient received approximately 60 units of blood products, including packed RBCs, platelets, and fresh frozen plasma. She required ICU admission for disseminated intravascular coagulation (DIC), multiorgan failure, vasopressor support (norepinephrine and vasopressin), mechanical ventilation, and empirical broad-spectrum antibiotics. Outcome: The patient gradually improved, with hemodynamic stabilization, resolution of DIC, and normalization of renal and hepatic function. She was discharged in stable condition on postpartum day 11. Conclusion: This case demonstrates that hysterectomy may not always control catastrophic PPH. Early recognition of alternative bleeding sources, aggressive resuscitation, and multidisciplinary critical care are essential, especially in high-risk patients with thrombophilia, to improve survival in patients with refractory primary postpartum hemorrhage.},
     year = {2026}
    }
    

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    T1  - Near-Miss Maternal Mortality: Survival After Massive Postpartum Hemorrhage, Disseminated Intravascular Coagulopathy, and Multiorgan Failure
    AU  - Ibrahim Kattoush
    AU  - Haya Ewidat
    AU  - Ayat Fararjeh
    AU  - Malak Hamdan
    AU  - Khawlla Ghraeb
    AU  - Mohammed Alra’e
    AU  - Mohammad Saya’Reh
    AU  - Montaser Shrouf
    Y1  - 2026/08/24
    PY  - 2026
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    DO  - 10.11648/j.jgo.20261404.12
    T2  - Journal of Gynecology and Obstetrics
    JF  - Journal of Gynecology and Obstetrics
    JO  - Journal of Gynecology and Obstetrics
    SP  - 97
    EP  - 100
    PB  - Science Publishing Group
    SN  - 2376-7820
    UR  - https://doi.org/10.11648/j.jgo.20261404.12
    AB  - Background: Postpartum hemorrhage (PPH) is a leading cause of maternal morbidity and mortality worldwide. Primary PPH, occurring within the first 24 hours after delivery, is the most common form and may rapidly progress to disseminated intravascular coagulation (DIC), multiorgan failure, and maternal near-miss events if bleeding is not promptly controlled. Patients with underlying thrombophilia are at increased risk for severe hemorrhage and coagulopathy. Case Presentation: A 35-year-old gravida 8, para 4, aborta 3 woman with Factor V Leiden thrombophilia presented for elective induction of labor at 38+4 weeks. Antenatal care was suboptimal. She initially underwent vaginal delivery but was converted to Cesarean section due to labor complications. Immediately postpartum, she developed severe PPH secondary to uterine atony, unresponsive to uterotonics and balloon tamponade. Total abdominal hysterectomy was performed, but hemorrhage persisted. Interventions: Surgical re-exploration identified bleeding from the left infundibulopelvic ligament. Hemostasis was achieved via bilateral internal iliac artery ligation and left oophorectomy. The patient received approximately 60 units of blood products, including packed RBCs, platelets, and fresh frozen plasma. She required ICU admission for disseminated intravascular coagulation (DIC), multiorgan failure, vasopressor support (norepinephrine and vasopressin), mechanical ventilation, and empirical broad-spectrum antibiotics. Outcome: The patient gradually improved, with hemodynamic stabilization, resolution of DIC, and normalization of renal and hepatic function. She was discharged in stable condition on postpartum day 11. Conclusion: This case demonstrates that hysterectomy may not always control catastrophic PPH. Early recognition of alternative bleeding sources, aggressive resuscitation, and multidisciplinary critical care are essential, especially in high-risk patients with thrombophilia, to improve survival in patients with refractory primary postpartum hemorrhage.
    VL  - 14
    IS  - 4
    ER  - 

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Author Information
  • Departement of Surgery, Hebron University, Hebron, Palestine

  • Departement of Surgery, Hebron University, Hebron, Palestine

  • Departement of Surgery, Hebron University, Hebron, Palestine

  • Departement of Surgery, Hebron University, Hebron, Palestine

  • Departement of Surgery, Hebron University, Hebron, Palestine

  • Departement of Surgery, Hebron University, Hebron, Palestine

  • Departement of Surgery, Mansoura University, Hebron, Palestine

  • Departement of Obstetrics and Gynecology, Palestine Red Crescent Society, Hebron, Palestine