Data from: Ambulatory versus inpatient management of severe nausea and vomiting of pregnancy: a randomized control trial with patient preference arm
ABSTRACT Objective To determine whether ambulatory (outpatient, OP) treatment of severe nausea and vomiting of pregnancy (NVP) is as effective as inpatient (IP) care. Design Non-blinded randomized control trial (RCT) with patient preference arm Setting Multi-center Participants Women less than 20 we...
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Zusammenfassung: | ABSTRACT Objective To determine whether ambulatory (outpatient, OP)
treatment of severe nausea and vomiting of pregnancy (NVP) is as effective
as inpatient (IP) care. Design Non-blinded randomized control trial (RCT)
with patient preference arm Setting Multi-center Participants Women less
than 20 weeks pregnant with severe NVP and associated ketonuria Methods
Women participating in the RCT were randomized via web-based application
to either ambulatory or IP treatment. Women declining randomisation
entered the patient preference trial (PPT) arm. Protocols, data collection
and follow-up were the same for all participants. Main Outcome Measures
Primary outcome was reduction in Pregnancy Unique Quantification of Emesis
(PUQE) score at 48 hours. Secondary outcomes were duration of treatment;
improvement in symptom scores and ketonuria at 48 hours; re-attendances
within 7 days of discharge; and comparison of symptoms at 7 days post
discharge Results 152/174 eligible women agreed to participate with 77/152
(51%) recruited to the RCT and 79/152 (49%) to the PPT. Patients were
initially compared in 4 groups (randomized IP, randomized OP,
non-randomized IP and non-randomized OP). Comprehensive cohort analysis of
participants in the (RCT) and (PPT) did not demonstrate any differences in
patient demographics or baseline clinical characteristics. Pooled analysis
of IP versus OP groups showed no difference in reduction in PUQE score at
48 hours (p=0.86). There was no difference in change in eating score
(p=0.69), drinking score (p=0.77), wellbeing rating (p=0.64) or reduction
in ketonuria (p=0.47) at 48 hours, with no difference in duration of index
treatment episode (p=0.83) or re-attendances within 7 days (p=0.52).
Conclusions Ambulatory management is an effective alternative to inpatient
management of severe NVP. The trial also demonstrated that many women
requiring treatment for HG have a strong preferences regarding treatment
setting, which needs to be considered by care providers, especially given
the psychological impact of HG. |
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DOI: | 10.5061/dryad.c3g48 |