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Personalised perioperative care by e-health after intermediate-grade abdominal surgery: a multicentre, single-blind, randomised, placebo-controlled trial

Authors :
Wilhelmus J. H. J. Meijerink
Johanna M. van Dongen
Steven E. Schraffordt Koops
Hendrik J. Bonjer
Eva van der Meij
Peter M. van de Ven
Frederieke G. Schaafsma
Wouter K. G. Leclercq
Caroline B. Terwee
Marlies Y. Bongers
Judith A. F. Huirne
Johannes R. Anema
Esther C. J. Consten
Public and occupational health
Amsterdam Reproduction & Development (AR&D)
APH - Societal Participation & Health
ACS - Heart failure & arrhythmias
Epidemiology and Data Science
APH - Methodology
Surgery
ACS - Microcirculation
APH - Quality of Care
APH - Global Health
Obstetrics and gynaecology
ACS - Atherosclerosis & ischemic syndromes
Obstetrics and Gynaecology
Health Economics and Health Technology Assessment
APH - Health Behaviors & Chronic Diseases
AMS - Ageing and Morbidity
Division 6
RS: GROW - R4 - Reproductive and Perinatal Medicine
Obstetrie & Gynaecologie
MUMC+: MA Medische Staf Obstetrie Gynaecologie (9)
Source :
The Lancet (London), 392, 51-59, Obstetrical and Gynecological Survey, 74(3), 148-149. Lippincott Williams and Wilkins, The Lancet (London), 392, 10141, pp. 51-59, van der Meij, E, Anema, J R, Leclercq, W K G, Bongers, M Y, Consten, E C J, Schraffordt Koops, S E, van de Ven, P M, Terwee, C B, van Dongen, J M, Schaafsma, F G, Meijerink, W J H J, Bonjer, H J & Huirne, J A F 2018, ' Personalised perioperative care by e-health after intermediate-grade abdominal surgery : a multicentre, single-blind, randomised, placebo-controlled trial ', The Lancet, vol. 392, no. 10141, pp. 51-59 . https://doi.org/10.1016/S0140-6736(18)31113-9, Lancet, 392(10141), 51-59. Elsevier Limited, van der Meij, E, Anema, J R, Leclercq, W K G, Bongers, M Y, Consten, E C J, Schraffordt Koops, S E, van de Ven, P M, Terwee, C B, van Dongen, J M, Schaafsma, F G, Meijerink, W J H J, Bonjer, H J & Huirne, J A F 2019, ' Personalised perioperative care by E-health after intermediate-grade abdominal surgery: A multicentre, single-blind, randomised, placebo-controlled trial ', Obstetrical and Gynecological Survey, vol. 74, no. 3, pp. 148-149 . https://doi.org/10.1097/01.ogx.0000554458.03689.ab, Van Der Meij, E, Anema, J R, Leclercq, W K G, Bongers, M Y, Consten, E C J, Schraffordt Koops, S E, Van De Ven, P M, Terwee, C B, Van Dongen, J M, Schaafsma, F G, Meijerink, W J H J, Bonjer, H J & Huirne, J A F 2019, ' Personalised perioperative care by E-health after intermediate-grade abdominal surgery : A multicentre, single-blind, randomised, placebo-controlled trial ', Obstetrical and Gynecological Survey, vol. 74, no. 3, pp. 148-149 . https://doi.org/10.1097/01.ogx.0000554458.03689.ab, van der Meij, E, Anema, J R, Leclercq, W K G, Bongers, M Y, Consten, E C J, Koops, S E S, van de Ven, P M, Terwee, C B, van Dongen, J M, Schaafsma, F G, Meijerink, W J H J, Bonjer, H J & Huirne, J A F 2018, ' Personalised perioperative care by e-health after intermediate-grade abdominal surgery : a multicentre, single-blind, randomised, placebo-controlled trial ', Lancet, vol. 392, no. 10141, pp. 51-59 . https://doi.org/10.1016/S0140-6736(18)31113-9, The Lancet, 392(10141), 51-59. Elsevier Limited, Lancet, 392(10141), 51-59. Elsevier Science
Publication Year :
2017

Abstract

BACKGROUND: Instructing and guiding patients after surgery is essential for successful recovery. However, the time that health-care professionals can spend with their patients postoperatively has been reduced because of efficiency-driven, shortened hospital stays. We evaluated the effect of a personalised e-health-care programme on return to normal activities after surgery.METHODS: A multicentre, single-blind, randomised controlled trial was done at seven teaching hospitals in the Netherlands. Patients aged 18-75 years who were scheduled for laparoscopic cholecystectomy, inguinal hernia surgery, or laparoscopic adnexal surgery for a benign indication were recruited. An independent researcher randomly allocated participants to either the intervention or control group using computer-based randomisation lists, with stratification by sex, type of surgery, and hospital. Participants in the intervention group had access to a perioperative, personalised, e-health-care programme, which managed recovery expectations and provided postoperative guidance tailored to the patient. The control group received usual care and access to a placebo website containing standard general recovery advice. Participants were unaware of the study hypothesis and were asked to complete questionnaires at five timepoints during the 6-month period after surgery. The primary outcome was time between surgery and return to normal activities, measured using personalised patient-reported outcome measures. Intention-to-treat and per-protocol analyses were done. This trial is registered in the Netherlands National Trial Register, number NTR4699.FINDINGS: Between Aug 24, 2015, and Aug 12, 2016, 344 participants were enrolled and randomly allocated to either the intervention (n=173) or control (n=171) group. 14 participants (4%) were lost to follow-up, with 330 participants included in the primary outcome analysis. Median time until return to normal activities was 21 days (95% CI 17-25) in the intervention group and 26 days (20-32) in the control group (hazard ratio 1·38, 95% CI 1·09-1·73; p=0·007). Complications did not differ between groups.INTERPRETATION: A personalised e-health intervention after abdominal surgery speeds up the return to normal activities compared with usual care. Implementation of this e-health programme is recommended in patients undergoing intermediate-grade abdominal, gynaecological, or general surgical procedures.FUNDING: ZonMw.

Details

ISSN :
1474547X, 01406736, and 00297828
Volume :
392
Issue :
10141
Database :
OpenAIRE
Journal :
Lancet (London, England)
Accession number :
edsair.doi.dedup.....8213933d41b95ce6b0fd4028474fc65f
Full Text :
https://doi.org/10.1016/S0140-6736(18)31113-9