the Efficacy and Safety of the 3-steps Conservative Approach in the Management of Placenta Accreta Spectrum (a Novel Technique)

NCT ID: NCT05191316

Last Updated: 2022-01-13

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 28 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2022-02-15
• Study Completion Date: 2022-05-15

Brief Summary

Placenta accrete spectrum (PAS) is an heterogeneous condition associated with a high maternal morbidity and mortality rate, presenting unique challenges in its diagnosis and management (Morlandoi et al., 2020). PAS describes a clinical situation where the placenta does not detach spontaneously after delivery and cannot be forcibly removed without causing massive and potentially life-threatening bleeding (Jauniaux et al., 2018), in this study we study a novel 3-step technique for surgical conservative management of PAS, in terms of efficacy and safety.

Detailed Description

• Informed written consent: after discussing the nature of the study as well as the expected value, outcome, and possible adverse effects.
• Full medical history: including full obstetric history and current pregnancy history (entailing the 1st day of LMP).
• Thorough Clinical Examination: general (maternal body weight and vital signs) and full obstetric examination.
• Obstetric ultrasonography: to confirm gestational age and the eligibility of the current pregnancy to participate in the study together with full placental assessment (diagnosis of PAS - placentation site and vasculature - extent of invasion to myometrial wall and surrounding structures as bladder wall invasion), with intra-operative confirmation aided by whether placental separation will occur or not.
• Preoperative laboratory tests: including prothrombin time, prothrombin concentration, complete blood count, and liver and kidney function tests.
• Operative steps: (A novel conservative 3 step technique)

• Patient positioning: under spinal anesthesia, the patient will be placed in the dorsal supine position. The patient will be then prepped and draped in the usual fashion for an abdominal procedure.
• A vertical midline incision will be done.
• Abdominal wall will be dissected in layers using sharp dissection or electro-coagulation instruments till the entry of peritoneal cavity.
• Dissection and release of the adherent bladder from the anterior uterine wall as low as possible (vesico-uterine peritoneal fold) together with the vascular disconnection of the newly formed vessels connecting the adherent invasive placenta to the urinary bladder. Dissection will be carried out laterally until both ureters are reached out and identified and in the midline until the lower edge of the placenta is identified.
• Transverse uterine incision above the upper border of placenta will be done followed by delivery of the fetus and immediate cord clamping (< 30 seconds) then the uterus will be exteriorized without trying to separate the adherent placenta and the uterine incision will be approximated by four towel clips (to reduce the blood loss).
• Placental bed devascularization (step 1): ligation of uterine arteries on two levels (one immediately under the lower level of placenta and another at least 5 mm above the upper edge of the adherent part of the placenta (superior-vesical arteries, feeding vessels of the placenta invading the back of the bladder will be also ligated).
• Cervical control sutures (step 2): transverse suture (full thickness) in the lower uterine segment at least 5 mm below the lower border of the placenta with or without similar stitch in the posterior uterine wall just above the uterosacral ligaments attachments.
• Delivery of the placenta with trimming of the invaded parts of the myometrium (step 3) followed by compression sutures taken in bleeding placental bed (if present) then myometrial reconstruction is done via continuous suture and mattress sutures.
• Bilateral ligation of the internal iliac arteries (4 cm distal to its origin) will be done if there is insufficient hemostasis is still present in spite of the above-mentioned steps to enhance further pelvic devascularization or if there's frank bladder invasion.
• In case of uncontrolled bleeding or failed the above-mentioned measures, hysterectomy will be done.
• Closure of abdominal wall in layers
• For all patients, 1 gm (10 ml) Tranexamic acid (Kapron, Amoun, Egypt) diluted in 20 ml of Glucose 5% will be given as intravenous infusion over 5 minutes, at least 15 minutes prior to skin incision in addition to 400 microgram misoprostol (2 tablets - Cytotec, Pfizer, G.D. Searle LLC) will administered rectally together with catheter insertion. Following the delivery of the baby, patients will receive an intravenous bolus of 5 IU oxytocin (Syntocinon, Novartis, Basel, Switzerland) and 20 IU oxytocin in 500mL lactated Ringer's solution (infused at a rate of 125mL/h).
• The operative steps (operative procedure, operative time, time interval between skin incision and fetal delivery, internal iliac artery ligation) will be recorded. The number and the difference of weight of operative towels (before and after CS) and amount of blood in suction unit will be also recorded.
• The received blood units or blood products will be recorded (intra or postoperative).
• Fluid monitoring will be performed through rate of infusion and urine output.
• The neonatal outcome (APGAR at 1 and 5 minutes, NICU admission and neonatal death) will be recorded.
• A complete blood count will be performed 12 hours after delivery. All patients will be followed up following the delivery as regard occurrence of primary postpartum hemorrhage (within the first 24 hours), re-exploration with further surgical procedures, the need for additional blood transfusion (within the first 24 hours) or ICU admission.
• Estimated Blood Loss (EBL) was evaluated as follows:

A. The number of operative towels used. B. The difference of weight of operative towels (before and after CS) plus the amount of blood in suction unit (we calculated 1 gram of weight difference equal to 1 ml blood loss).

C. EBL calculation according to the following formula:

EBL= EBV x Preoperative hematocrit- Postoperative hematocrit Postoperative hematocrit Where EBV is estimated blood volume of the patient in mL (equals weight in kg × 85).

• At least 6 weeks post-operatively, a 2D and 3D ultrasonographic assessment of the uterus will be done, assessing the uterine cavity (the presence and extend of a uterine niche). Trans-abdominal ultrasound complimented with trans-vaginal ultrasound, by an expert, using a Voluson E8 Expert (GE Healthcare Ultrasound Korea, Ltd) ultrasound will be done. All ultrasound findings will be recorded.
• Patients who the 3-step management fail and are managed by a cesarean hysterectomy will be considered and recorded as failed and will be excluded from the study.
• In avoidance of false positive PAS, an intra-operative confirmation will be done, should full placental separation or complete placenta accrete be found, those patients will be excluded from the study.

Conditions

Placenta Accreta, Third Trimester

Study Design

• Observational Model Type: OTHER
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• Patients aged 20-40 years old.
• Pregnant females with previous CS deliveries (at least 1) diagnosed with focal or partial PAS (placenta accreta/increta/percreta) candidate for 3rd trimester cesarean delivery.
• Patients wishing uterine conservation to preserve fertility.
• Gestational age: > 28 weeks confirmed by the 1st day of the LMP or 1st trimesteric ultrasound scan.
• Singleton pregnancies.
• CS under general anesthesia.

Exclusion Criteria

• Maternal Anemia (hemoglobin < 10 g %).
• Chronic or pregnancy induced medical disorders (e.g., cardiac, renal, DM and hepatic diseases).
• Patients presented with severe antepartum hemorrhage.
• Patients requested radical management (caesarean hysterectomy).
• Fetal death (IUFD).
• Fetal anomalies or IUGR (estimated fetal weight below the 5th centile).
• Women attending for emergency CS.
• Patients found to be suffering from placenta previa or total placenta accreta

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 40 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Cairo University

OTHER

Sponsor Role: lead

Responsible Party

Mohamed Essameldin Mohamed Abdullah

DR.

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Hassan M Gaafar, M.D

Role: PRINCIPAL_INVESTIGATOR

prof. of obstetrics and gynecology (Faculty of medicine -Cairo university)

Moataz M El-sherbini, M.D

Role: PRINCIPAL_INVESTIGATOR

prof. of obstetrics and gynecology (Faculty of medicine -Cairo university)

Abdalla m Mousa, M.D

Role: PRINCIPAL_INVESTIGATOR

lecturer of obstetrics and gynecology (Faculty of medicine -Cairo university)

mostafa E Abdalla, MRCOG

Role: PRINCIPAL_INVESTIGATOR

Senior specialist clinical fellow, gynecology Guy's and St. Thomas's NHS TRUST

Mazen m Abdel-rasheed, PhD

Role: PRINCIPAL_INVESTIGATOR

reproductive health research department, national research centre

sondos m salem, PhD

Role: PRINCIPAL_INVESTIGATOR

reproductive health research department, national research centre

Locations

Kasr al Ainy university, obstetrics and gynecology department

Cairo, Greater-cairo, Egypt

Countries

Egypt

Central Contacts

mohamed E abdullah, M.B.B.S.

Role: CONTACT

demk.93@gmail.com

0020-100-311-3995

Abdalla M Mousa, M.D

Role: CONTACT

dr_abdallamousa@yahoo.com

0020-127-766-4430

Facility Contacts

hassan M Gaafar, M.D

Role: primary

hassangaafar@kasralainy.edu.eg

00201001588300

Other Identifiers

MEMAbdullah

Identifier Type: -

Identifier Source: org_study_id