Atypical Presentation of Spontaneous Uterine Rupture Following a Spontaneous Vaginal Delivery

Research Article

Atypical Presentation of Spontaneous Uterine Rupture Following a Spontaneous Vaginal Delivery

  • Oyaromade A 1*
  • Fasanu O T 2
  • Usman M S 1
  • Isah M B 1
  • Ekele O I 1
  • Egwuete C O 1
  • Mohammed B A 2

*Corresponding Author: Oyaromade A, Nurse. Department of Obstetrics and Gynaeology, Ahmad Sanni Yariman Bakura Specialist Hospital, Gusau, Zamfara State.

Citation: Oyaromade A, Fasanu O T, Usman M S, Isah M B, Ekele O I, Egwuete C O and, Mohammed B A (2023). Mate Selection by Gender Role Journal of Clinical Case Reports and Studies 4(1); DOI: 10.31579/2690-8808/151

Copyright: © 2023 Oyaromade A, This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Received: 14 November 2022 | Accepted: 28 December 2022 | Published: 06 January 2023

Keywords:

Abstract

Introduction

Rupture of the pregnant uterus refers to complete disruption of all uterine layers, including the serosa [1]. It is an Obstetric catastrophe associated with high maternal and perinatal morbidity and mortality [2]. It is a common complication in the developing countries due to poor obstetric care, low socioeconomic status, ignorance and adverse sociocultural practices, beliefs and aversion for Caesarean section [2].

We are reporting a case of spontaneous uterine rupture following a spontaneous vaginal delivery that was managed at the department of Obstetrics and Gynaecology, Ahmad Sanni Yariman Bakura Specialist Hospital, Gusau, Zamfara state, Nigeria.

Case Presentation

Mrs A. A, a 25-year-old unbooked P4+0(2 alive) who had an unsupervised home delivery of a fresh male stillborn 9 days prior to presentation. She presented to the Obstetric emergency with lower abdominal pain of 9 days, fever, headache and diarrhoea of 8 days, no excessive vaginal bleeding. On examination, she was ill-looking, Temperature was 39.3°C, Pulse rate was 89bpm, BP- 120/90mmHg, there was generalized abdominal tenderness and she had normal lochia on vaginal examination. PCV was 32%. Ultrasound showed that pelvic organs were within normal limits but there was increased peritoneal fluid. She was admitted for puerperal sepsis and placed on parenteral antibiotics and analgesics.

1 day into admission, she was reviewed, she was still having abdominal pain and fever, on examination she was not pale, she had tinge of jaundice, pulse rate was 86bpm, BP- 120/90mmHg, abdomen was tender, uterus was difficult to palpate, percussion note was dull. The cervix was 6cm dilated. Ultrasound scan and PCV was to be repeated.

Day 2 into admission, she was still having fever, abdominal distention and pain. The repeat ultrasound scan showed a bulky uterus and a discontinuation in the lower part of the posterior wall of the uterus with massive peritoneal fluid, repeat PCV was 31%. On examination, she was not pale, had a tinge of jaundice, temperature was 38.0°C, pulse rate was 116bpm, BP- 110/80mmHg, there was generalized abdominal tenderness. On peritoneal tapping altered blood was obtained. 

                                                                                                                                 Figure 1

She subsequently had an emergency exploratory laparotomy with a midline sub-umbilical incision. Findings were massive haemoperitoneum of 2 litres, bulky uterus with left posterolateral rupture from the isthmus to the left cornu, gangrenous left fallopian tube and ovary, cheesy omental cake covering the uterus and the intra-abdominal organs. She had a total abdominal hysterectomy, left salpingo-oophorectomy and peritoneal toileting with a drain. She had 500mls of whole blood transfused intra-operatively. She was placed on antibiotics, IV fluids and analgesics. Drained was removed 2 days post op when it was no longer active. She did remarkably well and was discharged 1-week post op in good health condition.

Discussion

Uterine rupture is an uncommon complication of pregnancy, it's prevalence varies from one region and country to another [3]. It is rare in developed countries, however, it is a menace to developing countries especially in Africa where studies put the range between 0.3-2.4% [3-8].

In the developing countries, majority of cases of uterine rupture occur following prolonged obstructed labour whereas in developed countries, it occurs more often with a history of previous uterine surgeries [4,9]. Other risk factors for uterine rupture are, injudicious uterotonic use[3], grand multiparity, macrosomia [10,11], abnormal placention [12,13], and drug abuse [14,15]. However, none of these was identified in the patient presented.

Though majority of cases of uterine ruptures are diagnosed in the intrapartum period, only a few cases are diagnosed in the postpartum period [16]. Also, most patients present with the typical features of sudden abdominal pain, vaginal bleeding, deranged maternal vital signs and fetal heart rate abnormality or death, but a few cases do not present this way [17]. In the case presented above, the patient presented 9 days after a spontaneous vaginal delivery, she had no vaginal bleeding nor any haemodynamic instability, this contributed to the delay in making the diagnosis of a uterine rupture.

Due to the rare occurrence and the atypical presentation of lower abdominal pain, fever, headache and diarrhoea, and findings of normal vital signs with no vaginal bleeding our primary diagnosis was puerperal sepsis. Ultrasound scan showing massive intraperitoneal fluid and a peritoneal tap yielding altered blood subsequently raised the diagnosis of a uterine rupture.

The pathogenesis of the rupture was not known, however with the practice of fundal pressure being very common in our environment [18], she might have sustained the uterine rupture in the second stage of labour on account of fundal pressure, this was probably the reason she subsequently progressed to a spontaneous vaginal delivery of a fresh still birth. A similar case was reported in Taiwan [19]. It is however unclear why she had neither vaginal bleeding nor haemodynamic instability despite massive haemoperitoneum later detected on emergency laparotomy. 

Most cases of uterine rupture could be prevented with good antenatal care, birth preparedness and complication readiness, early recognition of obstructed labour, close monitoring of interventions known to have increased risk of uterine rupture [20]. Prompt diagnosis and treatment would prevent the accompanying morbidity and/or mortality. 

In conclusion, uterine rupture is an uncommon complication of pregnancy with high maternal and perinatal morbidity and mortality. They may present with unusual signs and symptoms making it tough to diagnose with history and physical examinations only. However, there should be a high index of suspicion of uterine rupture in a pregnant woman or in the puerperium with severe generalized abdominal with or without vaginal bleeding.

 

Conflict of interest

None.

Sponsorship

None.

References

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