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DOI 10.1136/bmjopen-2021-055664

Медицинская библиотека · BMJ open · 2022

Families' healthcare experiences for children with inherited metabolic diseases: protocol for a mixed methods cohort study.

Chow Andrea J, Iverson Ryan, Lamoureux Monica, Tingley Kylie, Jordan Isabel, Pallone Nicole, Smith Maureen, Al-Baldawi Zobaida, Chakraborty Pranesh, Brehaut Jamie, Chan Alicia, Cohen Eyal, Dyack Sarah, Gillis Lisa Jane, Goobie Sharan, Graham Ian D, Greenberg Cheryl R, Grimshaw Jeremy M, Hayeems Robin Z, Jain-Ghai Shailly, Jolly Ann, Khangura Sara, MacKenzie Jennifer J, Major Nathalie, Mitchell John J, Nicholls Stuart G, Pender Amy, Potter Murray, Prasad Chitra, Prosser Lisa A, Schulze Andreas, Siriwardena Komudi, Sparkes Rebecca, Speechley Kathy, Stockler Sylvia, Taljaard Monica, Teitelbaum Mari, Trakadis Yannis, van Karnebeek Clara, Walia Jagdeep S, Wilson Brenda J, Wilson Kumanan, Potter Beth K

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

INTRODUCTION

Children with inherited metabolic diseases (IMDs) often have complex and intensive healthcare needs and their families face challenges in receiving high-quality, family centred health services. Improvement in care requires complex interventions involving multiple components and stakeholders, customised to specific care contexts. This study aims to comprehensively understand the healthcare experiences of children with IMDs and their families across Canada.

METHODS AND ANALYSIS: A two-stage explanatory sequential mixed methods design will be used. Stage 1: quantitative data on healthcare networks and encounter experiences will be collected from 100 parent/guardians through a care map, 2 baseline questionnaires and 17 weekly diaries over 5-7 months. Care networks will be analysed using social network analysis. Relationships between demographic or clinical variables and ratings of healthcare experiences across a range of family centred care dimensions will be analysed using generalised linear regression. Other quantitative data related to family experiences and healthcare experiences will be summarised descriptively. Ongoing analysis of quantitative data and purposive, maximum variation sampling will inform sample selection for stage 2: a subset of stage 1 participants will participate in one-on-one videoconference interviews to elaborate on the quantitative data regarding care networks and healthcare experiences. Interview data will be analysed thematically. Qualitative and quantitative data will be merged during analysis to arrive at an enhanced understanding of care experiences. Quantitative and qualitative data will be combined and presented narratively using a weaving approach (jointly on a theme-by-theme basis) and visually in a side-by-side joint display.

ETHICS AND DISSEMINATION: The study protocol and procedures were approved by the Children's Hospital of Eastern Ontario's Research Ethics Board, the University of Ottawa Research Ethics Board and the research ethics boards of each participating study centre. Findings will be published in peer-reviewed journals and presented at scientific conferences.

Для цитирования: Chow Andrea J, Iverson Ryan, Lamoureux Monica, Tingley Kylie, Jordan Isabel, Pallone Nicole, Smith Maureen, Al-Baldawi Zobaida, Chakraborty Pranesh, Brehaut Jamie, Chan Alicia, Cohen Eyal, Dyack Sarah, Gillis Lisa Jane, Goobie Sharan, Graham Ian D, Greenberg Cheryl R, Grimshaw Jeremy M, Hayeems Robin Z, Jain-Ghai Shailly, Jolly Ann, Khangura Sara, MacKenzie Jennifer J, Major Nathalie, Mitchell John J, Nicholls Stuart G, Pender Amy, Potter Murray, Prasad Chitra, Prosser Lisa A, Schulze Andreas, Siriwardena Komudi, Sparkes Rebecca, Speechley Kathy, Stockler Sylvia, Taljaard Monica, Teitelbaum Mari, Trakadis Yannis, van Karnebeek Clara, Walia Jagdeep S, Wilson Brenda J, Wilson Kumanan, Potter Beth K. Families' healthcare experiences for children with inherited metabolic diseases: protocol for a mixed methods cohort study.. BMJ open. 2022. DOI: 10.1136/bmjopen-2021-055664.

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