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Maternal and neonatal consequences of treated and untreated asymptomatic bacteriuria in pregnancy: a prospective cohort study with an embedded randomised controlled trial

Authors :
Kazemier, B.M.
Koningstein, F.N.
Schneeberger, C.
Ott, A.
Bossuyt, P.M.
Miranda, E. de
Vogelvang, T.E.
Verhoeven, C.J.
Langenveld, J.
Woiski, M.D.
Oudijk, M.A.
Ven, J.E. van der
Vlegels, M.T.
Kuiper, P.N.
Feiertag, N.
Pajkrt, E.
Groot, C.J. de
Mol, B.W.
Geerlings, S.E.
Kazemier, B.M.
Koningstein, F.N.
Schneeberger, C.
Ott, A.
Bossuyt, P.M.
Miranda, E. de
Vogelvang, T.E.
Verhoeven, C.J.
Langenveld, J.
Woiski, M.D.
Oudijk, M.A.
Ven, J.E. van der
Vlegels, M.T.
Kuiper, P.N.
Feiertag, N.
Pajkrt, E.
Groot, C.J. de
Mol, B.W.
Geerlings, S.E.
Source :
Lancet Infectious Diseases; 1324; 1333; 1473-3099; 11; 15; ~Lancet Infectious Diseases~1324~1333~~~1473-3099~11~15~~
Publication Year :
2015

Abstract

Item does not contain fulltext<br />BACKGROUND: Existing approaches for the screening and treatment of asymptomatic bacteriuria in pregnancy are based on trials that were done more than 30 years ago. In this study, we reassessed the consequences of treated and untreated asymptomatic bacteriuria in pregnancy. METHODS: In this multicentre prospective cohort study with an embedded randomised controlled trial, we screened women (aged >/=18 years) at eight hospitals and five ultrasound centres in the Netherlands with a singleton pregnancy between 16 and 22 weeks' gestation for asymptomatic bacteriuria. Screening was done with a single dipslide and two culture media. Dipslides were judged positive when the colony concentration was at least 1x10(5) colony-forming units (CFU) per mL of a single microorganism or when two different colony types were present but one had a concentration of at least 1x10(5) CFU per mL. Asymptomatic bacteriuria-positive women were eligible to participate in the randomised controlled trial comparing nitrofurantoin with placebo treatment. In this trial, participants were randomly assigned 1:1 to receive either nitrofurantoin 100 mg or identical placebo tablets, and were instructed to self-administer these tablets twice daily for 5 consecutive days. Randomisation was done by a web-based application with a computer-generated list with random block sizes of two, four, or six participants rendered by an independent data manager. 1 week after the end of treatment, they provided us with a follow-up dipslide. Women, treating physicians, and researchers all remained unaware of the bacteriuria status and treatment allocation. Women who refused to participate in the randomised controlled trial did not receive any antibiotics, but their outcomes were collected for analysis in the cohort study. We compared untreated and placebo-treated asymptomatic bacteriuria-positive women with asymptomatic bacteriuria-negative women and nitrofurantoin-treated asymptomatic bacteriuria-positive women. The prima

Details

Database :
OAIster
Journal :
Lancet Infectious Diseases; 1324; 1333; 1473-3099; 11; 15; ~Lancet Infectious Diseases~1324~1333~~~1473-3099~11~15~~
Publication Type :
Electronic Resource
Accession number :
edsoai.on1284043360
Document Type :
Electronic Resource