Patient experience in bariatric surgery: protocol of a French narrative inquiry and qualitative analysis

被引:0
|
作者
Vignot, Marina [1 ,2 ]
Jung, Camille [1 ,2 ]
Bathaei, Sarah [3 ]
Lazzati, Andrea [3 ]
Gateau, Valerie [1 ]
Angeli, Frederica [4 ]
Delorenzo, Christian [5 ]
机构
[1] CHI Creteil, Clin Res Ctr, Creteil, France
[2] Univ Paris Est Creteil, Creteil, France
[3] CHI Creteil, Dept Gen Surg, Creteil, France
[4] Univ York, York, England
[5] CHI Creteil, Dept Psychiat, Creteil, France
来源
BMJ OPEN | 2024年 / 14卷 / 08期
关键词
bariatric surgery; quality in health care; patient-centred care; CANDIDATES;
D O I
10.1136/bmjopen-2023-082528
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction The quality of hospital care, especially surgery, is traditionally assessed using indicators derived from healthcare databases or safety indicators. Given the growing importance of placing the patient at the heart of care evaluation, the use of questionnaires such as the Patient-Reported Experience Measures and Patient-Reported Outcome Measures has become widespread in recent years. However, these tools-addressing factors such as satisfaction, pain management or wait times-only imperfectly reflect the patient's experience, and all such attempts at patient-centred care quality assessment rely on questions or indicators defined in advance by healthcare providers and health authorities. A biopsychosocial model may allow to better understand the patient experience and to improve care pathways. This study seeks to construct a narrative of the bariatric surgical care journey with instruments from narrative inquiry, propose a metanarrative that can serve as a basis for more sophisticated and reliable patient-focused care quality models and define indicators linked to patients' feelings and stories.Methods and analysis To achieve these aims, 16 bariatric surgical patients at the hospital of Cr & eacute;teil, France (Centre Hospitalier Intercommunal de Cr & eacute;teil), will be included and interviewed once before and twice after surgery, at months 3 and 6. Narratives collected will be used to construct a metanarrative intended to encompass all possible narratives. This metanarrative may ultimately inform new patient care quality indicators, furthering care focused on patients and tailored to their needs and predispositions.Ethics and dissemination The study is funded by the Group of Clinical Research and Innovation in & Icirc;le-de-France and was approved by CPP SUD-EST VI Clermont-Ferrand (France) Research Ethics Committee. The results will be submitted for publication in peer-reviewed journals. The patient associations will be approached for the dissemination of the study results.Trial registration number NCT05092659.
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页数:5
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