Prophylactic antibiotics to reduce pelvic infection in women having miscarriage surgery – The AIMS (Antibiotics in Miscarriage Surgery) trial: study protocol for a randomized controlled trial
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Date
2018Author
Lissauer, David
Wilson, Amie
Daniels, Jane
Middleton, Lee
Bishop, Jon
Hewitt, Catherine
Merriel, Abi
Weeks, Andrew
Mhango, Chisale
Mataya, Ronald
Taulo, Frank
Ngalawesa, Theresa
Chirwa, Agatha
Mphasa, Colleta
Tambala, Tayamika
Chiudzu, Grace
Mwalwanda, Caroline
Mboma, Agnes
Qureshi, Rahat
Ahmed, Iffat
Ismail, Humera
Gulmezoglu, Metin
Oladapo, Olufemi T.
Mbaruku, Godfrey
Chibwana, Jerome
Watts, Grace
Simon, Beatus
Ditai, James
Otim, Tom Charles
Acam, Jane-Frances
Ekunait, John
Uniza, Helen
Iyaku, Margaret
Anyango, Margaret
Zamora, Javier
Roberts, Tracy
Goranitis, Ilias
Desmond, Nicola
Coomarasamy, Arri
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Abstract
Background: The estimated annual global burden of miscarriage is 33 million out of 210 million pregnancies. Many
women undergoing miscarriage have surgery to remove pregnancy tissues, resulting in miscarriage surgery being
one of the most common operations performed in hospitals in low-income countries. Infection is a serious consequence
and can result in serious illness and death. In low-income settings, the infection rate following miscarriage surgery has
been reported to be high.
Good quality evidence on the use of prophylactic antibiotics for surgical miscarriage management is not available. Given
that miscarriage surgery is common, and infective complications are frequent and serious, prophylactic antibiotics may
offer a simple and affordable intervention to improve outcomes.
Methods: Eligible patients will be approached once the diagnosis of miscarriage has been made according to local
practice. Once informed consent has been given, participants will be randomly allocated using a secure internet facility
(1:1 ratio) to a single dose of oral doxycycline (400 mg) and metronidazole (400 mg) or placebo. Allocation will be
concealed to both the patient and the healthcare providers. A total of 3400 women will be randomised, 1700 in each
arm. The medication will be given approximately 2 hours before surgery, which will be provided according to local
practice. The primary outcome is pelvic infection 2 weeks after surgery. Women will be invited to the hospital for a
clinical assessment at 2 weeks. Secondary outcomes include overall antibiotic use, individual components of the primary
outcome, death, hospital admission, unplanned consultations, blood transfusion, vomiting, diarrhoea, adverse events,
anaphylaxis and allergy, duration of clinical symptoms, and days before return to usual activities. An economic evaluation
will be performed to determine if prophylactic antibiotics are cost-effective
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