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Conservative Surgical Novel Technique of Placenta Accreta in Menoufia University Hospital

Primary Purpose

Placenta Accreta

Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Novel Technique of Placenta Accreta in Menoufia University Hospital
Sponsored by
Menoufia Obstetrics and Gynecology Group
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Placenta Accreta

Eligibility Criteria

20 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • 1- Age between 20 - 40 years old. 2- Gestational age between 28 - 38 weeks. 3- Any patient diagnosed as placenta previa with ultrasound criteria of accretion.

    • Criteria of accretion by Colour Doppler ultrasound include: (Berkley et al., 2013).

      1. The presence of irregular shaped placental lacunae within the placenta.
      2. Thinning of myometrium overlying the placenta.
      3. Absence of retroplacental 'non-lucent line'.
      4. Protrusion of the placenta into the bladder.
      5. Increased vascularity of the uterine serosa-bladder interface.
      6. Turbulent blood flow through the lacunae on Doppler ultrasonography.

        Exclusion Criteria:

Sites / Locations

  • Menoufia University hospital
  • Hamed Elsayed Ellakwa

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Placenta Accreta patients

Arm Description

of 60 pregnant female diagnosed as placenta previa accreta recuirted from Obstetrics and Gynecology Department , Menoufia University Hospital.

Outcomes

Primary Outcome Measures

Outcome variables: Need for conversion to hysterectomy.
control of bleeding and need for removal of uterus.
Blood Loss.
Amount of blood loss ,Number of packed red blood cells and blood products transfusion.

Secondary Outcome Measures

Intraoperative complications
urinary bladder injury, ureteric injury. Postoperative complications e.g ileus, sepsis

Full Information

First Posted
November 5, 2019
Last Updated
November 9, 2019
Sponsor
Menoufia Obstetrics and Gynecology Group
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1. Study Identification

Unique Protocol Identification Number
NCT04161521
Brief Title
Conservative Surgical Novel Technique of Placenta Accreta in Menoufia University Hospital
Official Title
Conservative Surgical Novel Technique of Placenta Accreta in Menoufia University Hospital
Study Type
Interventional

2. Study Status

Record Verification Date
November 2019
Overall Recruitment Status
Completed
Study Start Date
November 1, 2018 (Actual)
Primary Completion Date
November 1, 2019 (Actual)
Study Completion Date
November 1, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Menoufia Obstetrics and Gynecology Group

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Evaluation of maternal morbidity and mortality of our novel surgical procedure for conservative management of placenta accreta in our tertiary referral institute.
Detailed Description
A descripative cohort study which included 60 pregnant women recuirted from Obstetrics and Gynecology Department, Menoufia University Hospital and diagnosed as placenta previa accreta. • Ethical considerations: Ethics: The study was approved by Ethical Committee of Menoufia Faculty of Medicine. Consent: after explanation of surgical procedure of the study, an informed written consent was obtained from all cases included in this study. Sample size: (No= 60) Based on previous studies regarding MAP, The incidence of placenta accreta = 1/2500 , so the calculated sample size for this study was 59 which to be around 60 with confidence level 95% margin of error 5% (Pliskow S et al., 2009). Inclusion criteria: Age between 20 - 40 years old. Gestational age between 28 - 38 weeks. Any patient diagnosed as placenta previa with ultrasound criteria of accretion. Criteria of accretion by Colour Doppler ultrasound include: (Berkley et al., 2013). The presence of irregular shaped placental lacunae within the placenta. Thinning of myometrium overlying the placenta. Absence of retroplacental 'non-lucent line'. Protrusion of the placenta into the bladder. Increased vascularity of the uterine serosa-bladder interface. Turbulent blood flow through the lacunae on Doppler ultrasonography. All patients were subjected to the following: I. Detailed history taking: Personal history: name ,age, address, occupation, marietal status, number of children ,age of the youngest child, the gender of the children and special habbits of medical importance like smoking. Past history: past medical history (e.g. diabetes mellitus, hypertension, renal disease, liver disease and any systemic disease like cardiac or pulmonary diseases), past surgical history (any operation done before), blood transfusion, drugs taken and allergy from any drug. Family history: hypertension, diabetes mellitus, consanguinity. Menstrual history: LMP (the first day of last menstrual period), duration, frequency, regularity of period, presence of dysmenorrhea and EDD (the expected date of delivery). Obstetric history : gravidity, parity, number of deliveries, mode of delivery (normal vaginal delivery or cesarean delivery) , place of delivery, the reason for cesarean delivery, any operative complications, number of children and their gender , any neonatal complications, number of abortions, gestational age of them, if abortion followed by surgery like evacuation and curettage. II. Clinical examination: General examination: General condition. Vital signs including blood pressure, pulse, temperature. Height, weight and body mass index (BMI). Neck : thyroid gland, neck veins and pulsations. Chest : lung, heart, breasts. Upper and lower limbs (edema , varicosities). Abdominal examination : Inspection : Size, shape, pigmentation (linea nigra),stria gravidarum and scars (like cesarean section scars). Palpation: To detect tenderness, rigidity and fundal level. Auscultation: Fetal heart sounds. III. Investigations : Preoperative labaratory investigations like complete blood count (CBC), prothrombin time (PT), liver function, kidney function, virology and ECG. Obstetric ultrasound: Fetal observation : transabdominal pelvic ultrasound was performed to detect fetal presentation, lie, viability ( by observation of fetal heart movement), gestational age by measuring biparital diameter, femur length and abdominal circumference) and fetal weight. Placenta observation : site (anterior or posterior), position in realtion to internal os to determine type of placenta previa and colour Doppler to determine grade of accretion ( accrete, increta, percreta and focal aacretion) and criteria of accretion. Surgical Procedure: Uterine conservation required multidisciplinary team including the obstetrician, anasethetist and urologist in certain cases. Preoperative prophylactic antibiotic was given to study cases prior to skin incision tio avoid postoperative endometritis in the form of 2gm ampicillin. (ACOG, 2011) Preoperative blood cross matching as availability of adequate blood was mandatory. Operative Steps: Elective CS at 36 weeks to 37 weeks was done. Prior to delivery, two large bore venous lines were placed. General anasethia was recommended. Foley catheter was inserted. Sterilization by povidone- iodine scrub and toweling. Midline incision was done as it made field obvious. Incision of subcutaneous tissue and rectus sheath. Separation of two recti. Classical CS (vertical incision in the upper uterine segment) or high transverse uterine incision was done to decrease haemorrhage through placental bed and to avoid urinary bladder injury as it may be adherent to lower uterine segment in some cases. Delievery of the fetus by gental fundal pressure. At the delivery of the fetus 10 UI of oxytocin IV was injected to help uterus to contract and avoid postpartum atony and to decrease blood loss during delivery. No attempt to the deliver the placenta Exteriorization of uterus including placenta clamped. Two corners of the uterine incision, and the superior and inferior lips, were clamped immediately by four clamps. Opening of the broad ligament via round ligament division and ligation. Gentle dissection of the bladder from the uterus was performed from lateral aspect to medially. Bilateral uterine artery clamping at below the placental bed Continue gentle dissection the remaining adherent part of the urinary bladder Gentle attempt to delierve the placenta by gentle traction on clamp. If the placenta was delievered, bilateral uterine artery ligation at multiple levels and multiple square compression sutures (if needed) to control pacental bleeding bed . If the placenta was not delievered we did segmental ressection of lower uterine segment including the placenta. The affected area, once excised can be repaired and the patient was treated as though she had a classical cesarean delivery. Intraperitoneal drain was inserted for early detection of intraperitoneal hemorrhage or urine leak in case of cystotomy repair or possible ureteric injury. The amount of blood loss within 24 h after surgery was measured by the weight of blood-soaked disposable hip pads minus its own weight. Transfusion must include not only packed red blood cells (PRBC), but also fresh frozen plasma and/or cryoprecipitate to maintain in a 2:1 ratio to prevent dillutional coagulopathy Outcome variables: Demographic data e.g age, parity, body mass index (BMI). Amount of blood loss by measuring Hb preoperatively and after blood transfusion. Amount of blood loss intraoperative via amount and number of tampons used. Amount of blood and blood products transfusion. Hemeostasis and analegesia postoperatively. Duration of ambulation and audible intestinal sounds. Follow up of nishe at placental bed after 6 weeks via color Doppler Ultrasoumd. Intraoperative complications e.g urinary bladder injury, ureteric injury. Postoperative complications e.g ileus, sepsis. Need for conversion to hysterectomy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Placenta Accreta

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placenta Accreta patients
Arm Type
Other
Arm Description
of 60 pregnant female diagnosed as placenta previa accreta recuirted from Obstetrics and Gynecology Department , Menoufia University Hospital.
Intervention Type
Procedure
Intervention Name(s)
Novel Technique of Placenta Accreta in Menoufia University Hospital
Intervention Description
Classical CS to decrease haemorrhage from placental bed. Delievery of the fetus. At the delivery 10 UI of oxytocin IV will be injected. The placenta is not attempted to be delievered. Opening of the broad ligament via round ligament division and ligation. Gentle dissection of the urinary bladder from lateral to medial. Bilateral uterine artery clamping at low level below the placental bed . Gentle attempt to deliver The placenta. If the placenta is delievered we will do bilateral uterine artery ligation at multiple levels and multiple square compression sutures(if needed) for proper hemeostasis at the placental bed. Then closure of uterine incision. If the placenta is not delievered we will do segmental ressection of lower uterine segment including the placenta . Intraperitoneal drain insertion.
Primary Outcome Measure Information:
Title
Outcome variables: Need for conversion to hysterectomy.
Description
control of bleeding and need for removal of uterus.
Time Frame
30- 90 minutes
Title
Blood Loss.
Description
Amount of blood loss ,Number of packed red blood cells and blood products transfusion.
Time Frame
During operation and 24 hours postpartum.
Secondary Outcome Measure Information:
Title
Intraoperative complications
Description
urinary bladder injury, ureteric injury. Postoperative complications e.g ileus, sepsis
Time Frame
During operation and postpartum period.

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1- Age between 20 - 40 years old. 2- Gestational age between 28 - 38 weeks. 3- Any patient diagnosed as placenta previa with ultrasound criteria of accretion. Criteria of accretion by Colour Doppler ultrasound include: (Berkley et al., 2013). The presence of irregular shaped placental lacunae within the placenta. Thinning of myometrium overlying the placenta. Absence of retroplacental 'non-lucent line'. Protrusion of the placenta into the bladder. Increased vascularity of the uterine serosa-bladder interface. Turbulent blood flow through the lacunae on Doppler ultrasonography. Exclusion Criteria:
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hamed E Ellakwa
Organizational Affiliation
Menoufia
Official's Role
Study Director
Facility Information:
Facility Name
Menoufia University hospital
City
Shibīn Al Kawm
State/Province
Menoufia
ZIP/Postal Code
11111
Country
Egypt
Facility Name
Hamed Elsayed Ellakwa
City
Shibīn Al Kawm
ZIP/Postal Code
11111
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32842821
Citation
Elkhouly NI, Solyman AE, Anter ME, Sanad ZF, El Ghazaly AN, Ellakwa HE. A new conservative surgical approach for placenta accreta spectrum in a low-resource setting. J Matern Fetal Neonatal Med. 2022 Aug;35(16):3076-3082. doi: 10.1080/14767058.2020.1808616. Epub 2020 Aug 25.
Results Reference
derived

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Conservative Surgical Novel Technique of Placenta Accreta in Menoufia University Hospital

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