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Tourniquet Reduces Blood Loss in Postpartum Hemorrhage During Hysterectomy for Placenta Accreta

Completed
Conditions
Blood Loss Massive
Post Partum Hemorrhage
Placenta Accreta
Registration Number
NCT03707132
Lead Sponsor
University Tunis El Manar
Brief Summary

Monocentric prospective observational study comparing the use of tourniquet in low uterus segement versus standard procedure in hysterectomy owing to placenta accreta

Detailed Description

It is a monocentric prospective observational case-control study in the Department "C" of Gynecology and Obstetrics in the Maternity and Neonatology Center of Tunis during three years from October 2014 to September 2017.

All parturient were informed about the possibility of performing a hysterectomy if accretization was clinically confirmed preoperatively. After obtaining written formal consent. all patients who underwent scheduled or emergency cesarean section for placenta accreta were included. Either it was highly suspected or confirmed by obstetrical imaging. MRI was always performed in cases of scheduled cesarean delivery. However, in cases of delayed transfer or if parturient was already in labor, only ultrasonography was done and considered as sufficient. Delivery was usually scheduled at 36 weeks of gestation.

Patients were allocated into two group: Group TG in which a tourniquet was systematically applied on the lower segment of the uterus during emergent hysterectomy, control group CG when the emergent caesarian hysterectomy was performed without a tourniquet. Allocation depended on the technique and the decision of the surgeon in charge.

After appropriate conditioning and monitoring, the cesarean section was performed under general anesthesia. The laparotomy was performed through a mid-line incision from the umbilicus to the pubic symphysis. Hysterotomy was made far from the placental insertion which was previously located by ultrasonography. The accretization was clinically checked immediately after delivery but no attempt was made to manually remove the placenta. The umbilical cord was ligated to its insertion and the uterus was quickly sutured with the placenta kept in place. Careful detachment of the bladder-uterus peritoneum was then carried out in order to lower the bladder and reduce the risk of bladder wounds. Tourniquet application procedure is described as following

1. Suturing hysterotomy with placenta kept in place.

2. After a cautious dissection a Folley catheter is placed in the lower segment of the uterus as tourniquet.

3. complete hysterectomy

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
43
Inclusion Criteria
  • . All patients undergoing scheduled or emergency cesarean section for placenta accreta
Exclusion Criteria
  • No signs of accretetization upon artificial delivery

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Estimated blood lossperoperatively

Blood spoliation during procedure

Hemoglobin variationFirst 24 hours

the differnece between the Baseline concentration of Hemoglobin and the lowest hemoglobin concentration noted during the procedure

Transfusion requirementsFirst 24 hours

Number of red blood cells units transfused

procedure durationperoperatively

Time needed to perform hysterectomy from incision to skin closure

Intensive care transfer ratefirst 24 hours

Intensive care transfer following hysterectomy for placenta accreta

Secondary Outcome Measures
NameTimeMethod
length of stay in ICUtime from surgery up to 30 days postoperative

duration of the stay in the ICU following hysterectomy for placenta accreta

clotting disorderstime from surgery up to 30 days postoperative

Assessed by the incidence of Intravascular disseminated coagulopathy

Bladder woundtime from surgery up to 30 days postoperative

Incidence of accidental bladder damage

Digestive woundtime from surgery up to 30 days postoperative

Incidence of accidental digestive lesion

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