ObjectiveWe aimed to determine foetal losses for DCDA and MCDA twins following transabdominal CVS or amniocentesis performed 0 weeks.MethodsRetrospective cohort study conducted in the UK and Belgium 01/01/00-01/06/20. Cases with unknown chorionicity, monochorionic complications or complex procedures were excluded. Uncomplicated DCDA and MCDA twins without invasive procedures were identified as controls. We reported foetal losses 0 weeks and losses of genetically and structurally normal foetuses.ResultsOutcomes were compared for DCDA foetuses; 258 after CVS with 3406 controls, 406 after amniocentesis with 3390 controls plus MCDA foetuses, 98 after CVS with 1124 controls, and 160 after amniocentesis with 1122 controls. There were more losse...
OBJECTIVE: To compare the fetal loss rate <24 weeks and the preterm premature rupture of the memb...
OBJECTIVE: To assess the adverse pregnancy outcome of post-chorionic villus sampling (CVS) amnioce...
A (semi-) randomized controlled study with long-term follow-up was conducted to compare the effects ...
OBJECTIVE: We aimed to determine foetal losses for DCDA and MCDA twins following transabdominal CVS ...
Objectives: To assess the rate of fetal loss following amniocentesis and chorionic villous sampling ...
Objectives: To assess the rate of fetal loss following amniocentesis and chorionic villous sampling ...
Objectives To identify maternal-, operator-and procedure-related variables that affect procedure-rel...
To identify maternal-, operator- and procedure-related variables that affect procedure-related pregn...
Objective To assess the fetal loss rate following amnio-centesis and chorionic villus sampling (CVS)...
To estimate the chorionic villus sampling (CVS) related risk of fetal loss after adjustment for chor...
Objective To assess the rate of fetal loss following amniocentesis or chorionic villus sampling (CV...
Objective: To estimate the procedure-related risk of miscarriage in pregnancies undergoing amniocent...
Introduction: To estimate the procedure-related risks of pregnancy loss following chorionic villus s...
Objectives To identify maternal-, operator-and procedure-related variables that affect procedure-rel...
OBJECTIVE: To compare the fetal loss rate <24 weeks and the preterm premature rupture of the memb...
OBJECTIVE: To assess the adverse pregnancy outcome of post-chorionic villus sampling (CVS) amnioce...
A (semi-) randomized controlled study with long-term follow-up was conducted to compare the effects ...
OBJECTIVE: We aimed to determine foetal losses for DCDA and MCDA twins following transabdominal CVS ...
Objectives: To assess the rate of fetal loss following amniocentesis and chorionic villous sampling ...
Objectives: To assess the rate of fetal loss following amniocentesis and chorionic villous sampling ...
Objectives To identify maternal-, operator-and procedure-related variables that affect procedure-rel...
To identify maternal-, operator- and procedure-related variables that affect procedure-related pregn...
Objective To assess the fetal loss rate following amnio-centesis and chorionic villus sampling (CVS)...
To estimate the chorionic villus sampling (CVS) related risk of fetal loss after adjustment for chor...
Objective To assess the rate of fetal loss following amniocentesis or chorionic villus sampling (CV...
Objective: To estimate the procedure-related risk of miscarriage in pregnancies undergoing amniocent...
Introduction: To estimate the procedure-related risks of pregnancy loss following chorionic villus s...
Objectives To identify maternal-, operator-and procedure-related variables that affect procedure-rel...
OBJECTIVE: To compare the fetal loss rate <24 weeks and the preterm premature rupture of the memb...
OBJECTIVE: To assess the adverse pregnancy outcome of post-chorionic villus sampling (CVS) amnioce...
A (semi-) randomized controlled study with long-term follow-up was conducted to compare the effects ...