Self-Management of Postnatal Hypertension: The SNAP-HT Trial
Hypertension affects 1 in 10 pregnancies, often persisting postpartum, when antihypertensive requirements may vary substantially. This unmasked, randomized controlled trial evaluated the feasibility and effects on blood pressure (BP) of self-management of postpartum hypertension. Women with gestatio...
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Published in | Hypertension (Dallas, Tex. 1979) Vol. 72; no. 2; pp. 425 - 432 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Heart Association, Inc
01.08.2018
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Subjects | |
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Abstract | Hypertension affects 1 in 10 pregnancies, often persisting postpartum, when antihypertensive requirements may vary substantially. This unmasked, randomized controlled trial evaluated the feasibility and effects on blood pressure (BP) of self-management of postpartum hypertension. Women with gestational hypertension or preeclampsia, requiring postnatal antihypertensive treatment, were randomized to self-management or usual care. Self-management entailed daily home BP monitoring and automated medication reduction via telemonitoring. Women attended 5 follow-up visits during 6 months. The primary outcome was feasibilityspecifically recruitment, retention, and compliance with follow-up rates. Secondary outcomes included BP control and safety, analyzed on an intention-to-treat basis. Forty-nine percent (91/186) of those women approached were randomized (45 intervention, 46 control), and 90% (82/91) finished follow-up. The groups had similar baseline characteristics. After randomization, BP was lower in the intervention group, most markedly at 6 weeksintervention group mean (SD), systolic 121.6 (8.7)/diastolic 80.5 (6.6) mm Hg; control group, systolic 126.6 (11.0)/diastolic 86.0 (9.7) mm Hg; adjusted differences (95% confidence interval), systolic −5.2 (−9.3 to −1.2)/diastolic −5.8 (−9.1 to −2.5) mm Hg. Diastolic BP remained significantly lower in those self-managing to 6 monthsadjusted difference −4.5 (−8.1 to −0.8) mm Hg. This is the first randomized evaluation of BP self-management postpartum and indicates it would be feasible to trial this intervention in larger studies. Self-management resulted in better diastolic BP control to 6 months, even beyond medication cessation.
CLINICAL TRIAL REGISTRATION—URLhttp://www.clinicaltrials.gov. Unique identifierNCT02333240. |
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AbstractList | Hypertension affects 1 in 10 pregnancies, often persisting postpartum, when antihypertensive requirements may vary substantially. This unmasked, randomized controlled trial evaluated the feasibility and effects on blood pressure (BP) of self-management of postpartum hypertension. Women with gestational hypertension or preeclampsia, requiring postnatal antihypertensive treatment, were randomized to self-management or usual care. Self-management entailed daily home BP monitoring and automated medication reduction via telemonitoring. Women attended 5 follow-up visits during 6 months. The primary outcome was feasibility: specifically recruitment, retention, and compliance with follow-up rates. Secondary outcomes included BP control and safety, analyzed on an intention-to-treat basis. Forty-nine percent (91/186) of those women approached were randomized (45 intervention, 46 control), and 90% (82/91) finished follow-up. The groups had similar baseline characteristics. After randomization, BP was lower in the intervention group, most markedly at 6 weeks: intervention group mean (SD), systolic 121.6 (8.7)/diastolic 80.5 (6.6) mm Hg; control group, systolic 126.6 (11.0)/diastolic 86.0 (9.7) mm Hg; adjusted differences (95% confidence interval), systolic -5.2 (-9.3 to -1.2)/diastolic -5.8 (-9.1 to -2.5) mm Hg. Diastolic BP remained significantly lower in those self-managing to 6 months: adjusted difference -4.5 (-8.1 to -0.8) mm Hg. This is the first randomized evaluation of BP self-management postpartum and indicates it would be feasible to trial this intervention in larger studies. Self-management resulted in better diastolic BP control to 6 months, even beyond medication cessation.
URL: http://www.clinicaltrials.gov. Unique identifier: NCT02333240. Hypertension affects 1 in 10 pregnancies, often persisting postpartum, when antihypertensive requirements may vary substantially. This unmasked, randomized controlled trial evaluated the feasibility and effects on blood pressure (BP) of self-management of postpartum hypertension. Women with gestational hypertension or preeclampsia, requiring postnatal antihypertensive treatment, were randomized to self-management or usual care. Self-management entailed daily home BP monitoring and automated medication reduction via telemonitoring. Women attended 5 follow-up visits during 6 months. The primary outcome was feasibility: specifically recruitment, retention, and compliance with follow-up rates. Secondary outcomes included BP control and safety, analyzed on an intention-to-treat basis. Forty-nine percent (91/186) of those women approached were randomized (45 intervention, 46 control), and 90% (82/91) finished follow-up. The groups had similar baseline characteristics. After randomization, BP was lower in the intervention group, most markedly at 6 weeks: intervention group mean (SD), systolic 121.6 (8.7)/diastolic 80.5 (6.6) mm Hg; control group, systolic 126.6 (11.0)/diastolic 86.0 (9.7) mm Hg; adjusted differences (95% confidence interval), systolic -5.2 (-9.3 to -1.2)/diastolic -5.8 (-9.1 to -2.5) mm Hg. Diastolic BP remained significantly lower in those self-managing to 6 months: adjusted difference -4.5 (-8.1 to -0.8) mm Hg. This is the first randomized evaluation of BP self-management postpartum and indicates it would be feasible to trial this intervention in larger studies. Self-management resulted in better diastolic BP control to 6 months, even beyond medication cessation.Hypertension affects 1 in 10 pregnancies, often persisting postpartum, when antihypertensive requirements may vary substantially. This unmasked, randomized controlled trial evaluated the feasibility and effects on blood pressure (BP) of self-management of postpartum hypertension. Women with gestational hypertension or preeclampsia, requiring postnatal antihypertensive treatment, were randomized to self-management or usual care. Self-management entailed daily home BP monitoring and automated medication reduction via telemonitoring. Women attended 5 follow-up visits during 6 months. The primary outcome was feasibility: specifically recruitment, retention, and compliance with follow-up rates. Secondary outcomes included BP control and safety, analyzed on an intention-to-treat basis. Forty-nine percent (91/186) of those women approached were randomized (45 intervention, 46 control), and 90% (82/91) finished follow-up. The groups had similar baseline characteristics. After randomization, BP was lower in the intervention group, most markedly at 6 weeks: intervention group mean (SD), systolic 121.6 (8.7)/diastolic 80.5 (6.6) mm Hg; control group, systolic 126.6 (11.0)/diastolic 86.0 (9.7) mm Hg; adjusted differences (95% confidence interval), systolic -5.2 (-9.3 to -1.2)/diastolic -5.8 (-9.1 to -2.5) mm Hg. Diastolic BP remained significantly lower in those self-managing to 6 months: adjusted difference -4.5 (-8.1 to -0.8) mm Hg. This is the first randomized evaluation of BP self-management postpartum and indicates it would be feasible to trial this intervention in larger studies. Self-management resulted in better diastolic BP control to 6 months, even beyond medication cessation.URL: http://www.clinicaltrials.gov. Unique identifier: NCT02333240.CLINICAL TRIAL REGISTRATIONURL: http://www.clinicaltrials.gov. Unique identifier: NCT02333240. Hypertension affects 1 in 10 pregnancies, often persisting postpartum, when antihypertensive requirements may vary substantially. This unmasked, randomized controlled trial evaluated the feasibility and effects on blood pressure (BP) of self-management of postpartum hypertension. Women with gestational hypertension or preeclampsia, requiring postnatal antihypertensive treatment, were randomized to self-management or usual care. Self-management entailed daily home BP monitoring and automated medication reduction via telemonitoring. Women attended 5 follow-up visits during 6 months. The primary outcome was feasibility: specifically recruitment, retention, and compliance with follow-up rates. Secondary outcomes included BP control and safety, analyzed on an intention-to-treat basis. Forty-nine percent (91/186) of those women approached were randomized (45 intervention, 46 control), and 90% (82/91) finished follow-up. The groups had similar baseline characteristics. After randomization, BP was lower in the intervention group, most markedly at 6 weeks: intervention group mean (SD), systolic 121.6 (8.7)/diastolic 80.5 (6.6) mm Hg; control group, systolic 126.6 (11.0)/diastolic 86.0 (9.7) mm Hg; adjusted differences (95% confidence interval), systolic −5.2 (−9.3 to −1.2)/diastolic −5.8 (−9.1 to −2.5) mm Hg. Diastolic BP remained significantly lower in those self-managing to 6 months: adjusted difference −4.5 (−8.1 to −0.8) mm Hg. This is the first randomized evaluation of BP self-management postpartum and indicates it would be feasible to trial this intervention in larger studies. Self-management resulted in better diastolic BP control to 6 months, even beyond medication cessation. Hypertension affects 1 in 10 pregnancies, often persisting postpartum, when antihypertensive requirements may vary substantially. This unmasked, randomized controlled trial evaluated the feasibility and effects on blood pressure (BP) of self-management of postpartum hypertension. Women with gestational hypertension or preeclampsia, requiring postnatal antihypertensive treatment, were randomized to self-management or usual care. Self-management entailed daily home BP monitoring and automated medication reduction via telemonitoring. Women attended 5 follow-up visits during 6 months. The primary outcome was feasibilityspecifically recruitment, retention, and compliance with follow-up rates. Secondary outcomes included BP control and safety, analyzed on an intention-to-treat basis. Forty-nine percent (91/186) of those women approached were randomized (45 intervention, 46 control), and 90% (82/91) finished follow-up. The groups had similar baseline characteristics. After randomization, BP was lower in the intervention group, most markedly at 6 weeksintervention group mean (SD), systolic 121.6 (8.7)/diastolic 80.5 (6.6) mm Hg; control group, systolic 126.6 (11.0)/diastolic 86.0 (9.7) mm Hg; adjusted differences (95% confidence interval), systolic −5.2 (−9.3 to −1.2)/diastolic −5.8 (−9.1 to −2.5) mm Hg. Diastolic BP remained significantly lower in those self-managing to 6 monthsadjusted difference −4.5 (−8.1 to −0.8) mm Hg. This is the first randomized evaluation of BP self-management postpartum and indicates it would be feasible to trial this intervention in larger studies. Self-management resulted in better diastolic BP control to 6 months, even beyond medication cessation. CLINICAL TRIAL REGISTRATION—URLhttp://www.clinicaltrials.gov. Unique identifierNCT02333240. |
Author | Edwards, Claire Mollison, Jill Pullon, Rebecca Ashworth, Felicity Mort, Sam Salvi, Dario Mackillop, Lucy H. Santos, Mauro Tucker, Katherine L. Tarassenko, Lionel Tebbutt, Julie Lloyd, Sue McManus, Richard J. Baker, Natasha Velardo, Carmelo Crawford, Carole Cairns, Alexandra E. Selinger, Mark Leeson, Paul |
AuthorAffiliation | From the Nuffield Department of Primary Care Health Sciences (A.E.C., K.L.T., S.M., J.M., R.J.M.) Cardiovascular Clinical Research Facility (P.L.) Nuffield Department of Obstetrics and Gynaecology (L.H.M.) Institute of Biomedical Engineering (M.S., C.V., D.S., L.T.), University of Oxford, United Kingdom. University of Oxford University of Oxford Royal Berkshire NHS Foundation Trust Royal Berkshire NHS Foundation Trust Northampton General Hospital NHS Trust Buckinghamshire Healthcare NHS Trust Buckinghamshire Healthcare NHS Trust University of Oxford |
AuthorAffiliation_xml | – name: From the Nuffield Department of Primary Care Health Sciences (A.E.C., K.L.T., S.M., J.M., R.J.M.) Cardiovascular Clinical Research Facility (P.L.) Nuffield Department of Obstetrics and Gynaecology (L.H.M.) Institute of Biomedical Engineering (M.S., C.V., D.S., L.T.), University of Oxford, United Kingdom. University of Oxford University of Oxford Royal Berkshire NHS Foundation Trust Royal Berkshire NHS Foundation Trust Northampton General Hospital NHS Trust Buckinghamshire Healthcare NHS Trust Buckinghamshire Healthcare NHS Trust University of Oxford |
Author_xml | – sequence: 1 givenname: Alexandra surname: Cairns middlename: E. fullname: Cairns, Alexandra E. organization: From the Nuffield Department of Primary Care Health Sciences (A.E.C., K.L.T., S.M., J.M., R.J.M.) Cardiovascular Clinical Research Facility (P.L.) Nuffield Department of Obstetrics and Gynaecology (L.H.M.) Institute of Biomedical Engineering (M.S., C.V., D.S., L.T.), University of Oxford, United Kingdom. University of Oxford University of Oxford Royal Berkshire NHS Foundation Trust Royal Berkshire NHS Foundation Trust Northampton General Hospital NHS Trust Buckinghamshire Healthcare NHS Trust Buckinghamshire Healthcare NHS Trust University of Oxford – sequence: 2 givenname: Katherine surname: Tucker middlename: L. fullname: Tucker, Katherine L. – sequence: 3 givenname: Paul surname: Leeson fullname: Leeson, Paul – sequence: 4 givenname: Lucy surname: Mackillop middlename: H. fullname: Mackillop, Lucy H. – sequence: 5 givenname: Mauro surname: Santos fullname: Santos, Mauro – sequence: 6 givenname: Carmelo surname: Velardo fullname: Velardo, Carmelo – sequence: 7 givenname: Dario surname: Salvi fullname: Salvi, Dario – sequence: 8 givenname: Sam surname: Mort fullname: Mort, Sam – sequence: 9 givenname: Jill surname: Mollison fullname: Mollison, Jill – sequence: 10 givenname: Lionel surname: Tarassenko fullname: Tarassenko, Lionel – sequence: 11 givenname: Richard surname: McManus middlename: J. fullname: McManus, Richard J. – sequence: 12 givenname: Carole surname: Crawford fullname: Crawford, Carole – sequence: 13 givenname: Claire surname: Edwards fullname: Edwards, Claire – sequence: 14 givenname: Natasha surname: Baker fullname: Baker, Natasha – sequence: 15 givenname: Mark surname: Selinger fullname: Selinger, Mark – sequence: 16 givenname: Sue surname: Lloyd fullname: Lloyd, Sue – sequence: 17 givenname: Julie surname: Tebbutt fullname: Tebbutt, Julie – sequence: 18 givenname: Felicity surname: Ashworth fullname: Ashworth, Felicity – sequence: 19 givenname: Rebecca surname: Pullon fullname: Pullon, Rebecca |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29967037$$D View this record in MEDLINE/PubMed |
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Contributor | Tebbutt, Julie Edwards, Claire Lloyd, Sue Pullon, Rebecca Baker, Natasha Ashworth, Felicity Crawford, Carole Selinger, Mark |
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Copyright | 2018 American Heart Association, Inc 2018 American Heart Association, Inc. |
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Snippet | Hypertension affects 1 in 10 pregnancies, often persisting postpartum, when antihypertensive requirements may vary substantially. This unmasked, randomized... |
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SubjectTerms | Adult Antihypertensive Agents - therapeutic use Blood Pressure - physiology Blood Pressure Monitoring, Ambulatory - methods Female Follow-Up Studies Humans Hypertension, Pregnancy-Induced - drug therapy Hypertension, Pregnancy-Induced - physiopathology Pregnancy Prospective Studies Self-Management - methods Treatment Outcome |
Title | Self-Management of Postnatal Hypertension: The SNAP-HT Trial |
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