J. Villar et al., WHO antenatal care randomised trial for the evaluation of a new model of routine antenatal care, LANCET, 357(9268), 2001, pp. 1551-1564
Citations number
42
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Background We undertook a multicentre randomised controlled trial that comp
ared the standard model of antenatal care with a new model that emphasises
actions known to be effective in improving maternal or neonatal outcomes an
d has fewer clinic visits.
Methods Clinics in Argentina, Cuba, Saudi Arabia, and Thailand were randoml
y allocated to provide either the new model (27 clinics) or the standard mo
del currently in use (26 clinics). All women presenting for antenatal care
at these clinics over an average of 18 months were enrolled. Women enrolled
in clinics offering the new model were classified on the basis of history
of obstetric and clinical conditions. Those who did not require further spe
cific assessment or treatment were offered the basic component of the new m
odel, and those deemed at higher risk received the usual care for their con
ditions; however, all were included in the new-model group for the analyses
, which were by intention to treat. The primary outcomes were low birthweig
ht (<2500 g), pre-eclampsia/eclampsia, severe postpartum anaemia (<90 g/L h
aemoglobin), and treated urinary-tract infection. There was an assessment o
f quality of care and an economic evaluation.
Findings Women attending clinics assigned the new model (n = 12 568) had a
median of five visits compared with eight within the standard model (n = 11
958). More women in the new model than in the standard model were referred
to higher levels of care (13.4% vs 7.3%), but rates of hospital admission,
diagnosis, and length of stay were similar. The groups had similar rates o
f low birthweight (new model 7.68% vs standard model 7.14%; stratified rate
difference 0.96 [95% CI -0.01 to 1.92]), postpartum anaemia (7.59% vs 8.67
%; 0.32), and urinary-tract infection (5.95% vs 7.41%; -0.42 [-1.65 to 0.80
]). For pre-eclampsia/eclampsia the rate was slightly higher in the new mod
el (1.69% vs 1.38%; 0.21 [-0.25 to 0.67]). Adjustment by several confoundin
g variables did not modify this pattern. There were negligible differences
between groups for several secondary outcomes. Women and providers in both
groups were, in general, satisfied with the care received, although some wo
men assigned the new model expressed concern about the timing of visits. Th
ere was no cost increase, and in some settings the new model decreased cost
.
Interpretations Provision of routine antenatal care by the new model seems
not to affect maternal and perinatal outcomes. It could be implemented with
out major resistance from women and providers and may reduce cost.