A Core Outcome Set for Children With Feeding Tubes and Neurologic Impairment: A Systematic Review

Author:

Kapadia Mufiza Z.1,Joachim Kariym C.1,Balasingham Chrinna1,Cohen Eyal23456,Mahant Sanjay2346,Nelson Katherine247,Maguire Jonathon L.28910,Guttmann Astrid2345,Offringa Martin1

Affiliation:

1. Toronto Outcomes Research in Child Health (TORCH), Child Health Evaluative Sciences,

2. Division of Paediatric Medicine,

3. Paediatrics Outcomes Research Team, and

4. Institute of Health Policy, Management and Evaluation, and

5. Institute for Clinical Evaluative Sciences, Toronto, Ontario, Canada;

6. CanChild Centre for Childhood Disability Research, McMaster University, Hamilton, Ontario, Canada; and

7. Paediatric Advanced Care Team, Department of Paediatrics, The Hospital for Sick Children (SickKids), Toronto, Ontario, Canada;

8. Department of Paediatrics, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada;

9. Li Ka Shing Knowledge Institute, and

10. Department of Paediatrics, St. Michael’s Hospital, Toronto, Ontario, Canada

Abstract

CONTEXT: Uncertainty exists about the impacts of feeding tubes on neurologically impaired children. Core outcome sets (COS) standardize outcome selection, definition, measurement, and reporting. OBJECTIVE: To synthesize an evidence base of qualitative data on all outcomes selected and/or reported for neurologically impaired children 0 to 18 years living with gastrostomy/gastrojejunostomy tubes. DATA SOURCES: Medline, Embase, and Cochrane Register databases searched from inception to March 2014. STUDY SELECTION: Articles examining health outcomes of neurologically impaired children living with feeding tubes. DATA EXTRACTION: Outcomes were extracted and assigned to modified Outcome Measures in Rheumatology 2.0 Filter core areas; death, life impact, resource use, pathophysiological manifestations, growth and development. RESULTS: We identified 120 unique outcomes with substantial heterogeneity in definition, measurement, and frequency of selection and/or reporting: “pathophysiological manifestation” outcomes (n = 83) in 79% of articles; “growth and development” outcomes (n = 13) in 55% of articles; “death” outcomes (n = 3) and “life impact” outcomes (n = 17) in 39% and 37% of articles, respectively; “resource use” outcomes (n = 4) in 14%. Weight (50%), gastroesophageal reflux (35%), and site infection (25%) were the most frequently reported outcomes. LIMITATIONS: We were unable to investigate effect size of outcomes because quantitative data were not collected. CONCLUSIONS: The paucity of outcomes assessed for life impact, resource use and death hinders meaningful evidence synthesis. A COS could help overcome the current wide heterogeneity in selection and definition. These results will form the basis of a consensus process to produce a final COS.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

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