TY - JOUR
T1 - Prophylactic antibiotics to reduce pelvic infection in women having miscarriage surgery – The AIMS (Antibiotics in Miscarriage Surgery) trial
T2 - study protocol for a randomized controlled trial
AU - Lissauer, David
AU - Wilson, Amie
AU - Daniels, Jane
AU - Middleton, Lee
AU - Bishop, Jon
AU - Hewitt, Catherine
AU - Merriel, Abi
AU - Weeks, Andrew
AU - Mhango, Chisale
AU - Mataya, Ronald
AU - Taulo, Frank
AU - Ngalawesa, Theresa
AU - Chirwa, Agatha
AU - Mphasa, Colleta
AU - Tambala, Tayamika
AU - Chiudzu, Grace
AU - Mwalwanda, Caroline
AU - Mboma, Agnes
AU - Qureshi, Rahat
AU - Ahmed, Iffat
AU - Ismail, Humera
AU - Gulmezoglu, Metin
AU - Oladapo, Olufemi T.
AU - Mbaruku, Godfrey
AU - Chibwana, Jerome
AU - Watts, Grace
AU - Simon, Beatus
AU - Ditai, James
AU - Tom, Charles Otim
AU - Acam, Jane Frances
AU - Ekunait, John
AU - Uniza, Helen
AU - Iyaku, Margaret
AU - Anyango, Margaret
AU - Zamora, Javier
AU - Roberts, Tracy
AU - Goranitis, Ilias
AU - Desmond, Nicola
AU - Coomarasamy, Arri
PY - 2018/4/23
Y1 - 2018/4/23
N2 - 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. Discussion: This trial will assess whether a single dose of doxycycline (400 mg) and metronidazole (400 mg) taken orally 2 hours before miscarriage surgery can reduce the incidence of pelvic infection in women up to 2 weeks after miscarriage surgery.
AB - 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. Discussion: This trial will assess whether a single dose of doxycycline (400 mg) and metronidazole (400 mg) taken orally 2 hours before miscarriage surgery can reduce the incidence of pelvic infection in women up to 2 weeks after miscarriage surgery.
KW - Antibiotics
KW - Economic evaluation
KW - Low-income countries
KW - Miscarriage
KW - Miscarriage surgery
KW - Pelvic infection
KW - Placebo-controlled trial
KW - Randomised controlled trial
UR - http://www.scopus.com/inward/record.url?scp=85045761046&partnerID=8YFLogxK
U2 - 10.1186/s13063-018-2598-3
DO - 10.1186/s13063-018-2598-3
M3 - Article (Academic Journal)
C2 - 29685179
SN - 1745-6215
VL - 19
JO - Trials
JF - Trials
M1 - 245
ER -