Use of bilateral internal iliac artery balloon occlusion as a preventative measure for a high‑risk hydatidiform mole treated with surgical evacuation: A case report
Affiliations: Department of Obstetrics and Gynaecology, The Royal Wolverhampton NHS Trust, Heath Town, Wolverhampton, West Midlands WV10 0QP, UK, College of Medical and Dental Sciences, University of Birmingham, Birmingham B15 2TT, UK, Department of Intervention Radiology, The Royal Wolverhampton NHS Trust, Heath Town, Wolverhampton, West Midlands WV10 0QP, UK
- Published online on: August 31, 2021 https://doi.org/10.3892/wasj.2021.124
- Article Number: 53
Copyright: © Abdulrahman et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
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Gestational trophoblastic disease (GTD) encompasses conditions ranging from hydatidiform mole (HM), to malignant disease processes, such as invasive mole, choriocarcinoma, placental site trophoblastic and epithelioid trophoblastic tumours known collectively as gestational trophoblastic neoplasia. Molar pregnancies originate from villous trophoblasts, and are characterised by trophoblastic hyperplasia and abnormal chorionic villi resulting from the overexpression of paternal genetic material (1).
The classic features of a molar pregnancy are vaginal bleeding, hyperemesis and an enlarged uterus for the gestational age. HM most commonly affects women at extremes of child-bearing age (<20 and >35 years of age), with those who have had a previous molar pregnancy at risk (1).
HM requires a histological diagnosis; however, an ultrasound examination is helpful in the diagnosis and has reduced the mean gestational age at presentation. The main complications of HM include malignant potential and major haemorrhage. Due to central registration in the UK at specialised trophoblastic centres and the use of β-human chorionic gonadotropin (β-hCG) as a marker of HM, the cure rates are excellent. Suction curettage is the preferred surgical management treatment for complete hydatidiform moles (CHMs) and partial hydatidiform moles (PHMs). Medical management is only advised in the case of a PHM where foetal parts do not allow for suction. Despite the risk of bleeding associated with HM, the use of oxytocic infusions are not advised due to the potential of disseminating trophoblastic tissue (1). Minimal research has been undertaken on the use of bilateral internal iliac artery balloon occlusion (BIIABO) as a preventative measure in the management of high-risk molar pregnancies undergoing surgical evacuation. The procedure involves the placement of a balloon catheter into the internal iliac arteries bilaterally in order to reduce the haemorrhage risk (2). To the best of our knowledge, this is the first report of this treatment method for HM.
A 27-year-old Eastern European female (gravidity, 1; parity, 0) presented to the Royal Wolverhampton NHS Trust at 12/40 gestation following an abnormal booking scan. The ultrasound findings included a grossly enlarged uterus extending above the umbilicus (113 AP x127 mm), with the uterus filled with a semi solid mass containing cystic areas consistent with the ‘snowstorm’ appearances indicative of a HM (Fig. 1).
Transabdominal ultrasound images showing the characteristic ‘snowstorm appearance’ indicative of a hydatidiform mole.
Upon admission, she complained of a 2-day history of minimal brown discharge, nausea and mild generalised abdominal pain. She was known to have irregular periods. She was not using any methods of contraception and had no previous cervical smears. The patient and her partner were not consanguineous. There was no family history of GTD. Upon examination, her uterus appeared large for gestation with the symphysis-fundal height measuring ~26 weeks. The blood analysis revealed haemoglobin levels of 83, β-hCG levels of 2,263,570 IU/l and a blood group of A rhesus (Rh) negative.
Following discussion with the nearest STC, suction curettage was advised. She was considered a high-risk patient due to her anaemia upon admission and grossly elevated β-hCG levels, with a risk of having a major haemorrhage. Her case was therefore discussed with the Haematology and Interventional Radiology Department at the Royal Wolverhampton NHS Trust for a multi-disciplinary approach. Prior to surgical management, she was appropriately cross-matched, administered 2 units of packed red blood cells, and given prophylactic antibiotics in theatre.
To minimise risk of developing a haemorrhage, the interventional radiology team inserted bilateral internal iliac artery balloons. A total of 2x10 ml 1% lidocaine was used as a local anaesthetic. Ultrasound guided punctures of the common femoral arteries were performed by a consultant interventional radiologist with 5-French sheaths inserted into both sides (Fig. 2). Fogarty compliant balloons were inflated in the anterior division of each of the internal iliac arteries until the flow was abolished distally. She then underwent the surgical evacuation of retained products under transabdominal ultrasound guidance. The internal os of the cervix was mechanically dilated to Hegar number 12, followed by the suction evacuation of copious amounts of products and blood, with gentle curettage under ultrasound guidance transabdominally. Following the evacuation of the uterine contents, the balloon catheters and both sheaths were removed, and arterial punctures sealed with mynx grips.
Angiogram of the left internal iliac artery showing the branches of the uterine artery stretched around the hydatidiform mole, prior to placement of occlusion balloons. The letters LT in the image indicate the left internal iliac artery.
The estimated blood loss was 1.8 litres and 3 units of red blood cells were transfused in total. Anti-D prophylaxis was administered, as the patient was Rh negative. Additionally, she received an intravenous dose of tranexamic acid. The post-operatively haemoglobin levels were 94 g/l and a Kleihauer-Betke test was undertaken to measure the degree of potential foetal-maternal haemorrhage; the results were negative. A histological examination of samples obtained during surgery confirmed a CHM. The patient was advised to use barrier contraception for 6 months following the procedure. In accordance with the UK protocol, patient was referred to the nearest specialised GTD centre for repeat 2-weekly β-hCG tests, and was started on oral contraceptives. Her β-hCG levels markedly decreased from a pre-evacuation level of 2,263,570 to 14,101 IU/l on day 16 post-evacuation. The levels continued to decrease and reverted to normal 6 months later, whilst being followed-up by a STC. At 18-months following the procedure, the patient became pregnant. She gave birth at 40+1 weeks to a healthy baby via vaginal delivery with no complications. She continues to report normal 28-day menstrual cycles.
The use of BIIABO to minimise the risk of bleeding has been explored within obstetrics in the management of high-risk caesarean sections secondary to placental invasion (3,4). Despite the limited availability in the literature regarding its use in the management of HM, initial research into the use of BIIABO within emergency gynaecology is promising.
A single case report exists in the literature in which internal iliac arteries balloons were inserted prophylactically for a high-risk patient with HM undergoing suction curettage; however, despite a 1.1 litre blood loss, the balloons were not inflated and were removed thereafter (5). The patient however, received an oxytocin infusion following the evacuation of the uterine cavity. This raises discussion surrounding the favourability of BIIABO over alternatives, such as oxytocic infusions in achieving haemostasis.
Although much of the literature regarding BIIABO is encouraging, there have been certain safety concerns raised, most commonly thrombotic events. Internal iliac artery balloons have been associated with serious thromboembolic events, lower limb ischemia, puncture site complications (hematomas, false aneurysms and the dissection of femoral arteries) and other complications (6).
Anatomically, there have been suggestions that due to collateral circulation from the external iliac artery to the uterus, a common iliac artery balloon occlusion (CIABO) would provide better outcomes. Notably, a study comparing BIIABO, CIABO and no occlusion in placenta accreta managed by caesarean hysterectomy found that the mean blood loss was statistically significantly reduced only in the CIABO group (P<0.05) (4).
Although the National Institute for Health and Care Excellence (NICE) currently does not provide guidance on when to proceed with balloon occlusion in gynaecological or obstetric emergencies, the Royal College of Obstetricians and Gynaecologists (RCOG) has urged units to consider early or prophylactic interventional radiology as an important tool (6).
To the best of our knowledge, this is the first study to demonstrate the use of BIIABO as a preventative measure in the management of women with hydatidiform mole at risk of severe bleeding. The use of BIIABO in the prevention of bleeding for patients with HM undergoing suction curettage offers promise for better outcomes in the surgical management of molar pregnancies. However, due to the limited literature that exists around the topic, further extensive research is required before BIIABO can be considered a safe, reliable and effective intervention.
No funding was received.
Availability of data and materials
Data sharing is not applicable to this article, as no datasets were generated or analysed during the current study. Data are however, available from the authors upon reasonable request.
SA was involved in the writing of the first draft of the manuscript, in the literature review, and in the editing of the manuscript. ME was involved in the writing of the first draft of the manuscript and in the editing of the manuscript. JD was involved in the clinical management of the patient and in the editing of the manuscript. AEG was involved in the clinical management of the patient, obtaining consent from the patient and in the editing of the manuscript. SA, ME, JD and AEG confirm the authenticity of all the raw data. All authors have read and approved the final manuscript.
Ethics approval and consent to participate
The patient in the present case report provided informed consent.
Patient consent for publication
The patient in the present case report provided her consent for her data to be published.
The authors declare that they have no competing interests.
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