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Development of a proxy-reported pulmonary outcome scale for preterm infants with bronchopulmonary dysplasia
BACKGROUND: To develop an accurate, proxy-reported bedside measurement tool for assessment of the severity of bronchopulmonary dysplasia (also called chronic lung disease) in preterm infants to supplement providers' current biometric measurements of the disease. METHODS: We adapted Patient-Repo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161834/ https://www.ncbi.nlm.nih.gov/pubmed/21791099 http://dx.doi.org/10.1186/1477-7525-9-55 |
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author | Massie, Sara E Tolleson-Rinehart, Sue DeWalt, Darren A Laughon, Matthew M Powell, Leslie M Price, Wayne A |
author_facet | Massie, Sara E Tolleson-Rinehart, Sue DeWalt, Darren A Laughon, Matthew M Powell, Leslie M Price, Wayne A |
author_sort | Massie, Sara E |
collection | PubMed |
description | BACKGROUND: To develop an accurate, proxy-reported bedside measurement tool for assessment of the severity of bronchopulmonary dysplasia (also called chronic lung disease) in preterm infants to supplement providers' current biometric measurements of the disease. METHODS: We adapted Patient-Reported Outcomes Measurement Information System (PROMIS) methodology to develop the Proxy-Reported Pulmonary Outcomes Scale (PRPOS). A multidisciplinary group of registered nurses, nurse practitioners, neonatologists, developmental specialists, and feeding specialists at five academic medical centers participated in the PRPOS development, which included five phases: (1) identification of domains, items, and responses; (2) item classification and selection using a modified Delphi process; (3) focus group exploration of items and response options; (4) cognitive interviews on a preliminary scale; and (5) final revision before field testing. RESULTS: Each phase of the process helped us to identify, classify, review, and revise possible domains, questions, and response options. The final items for field testing include 26 questions or observations that a nurse assesses before, during, and after routine care time and feeding. CONCLUSIONS: We successfully created a prototype scale using modified PROMIS methodology. This process can serve as a model for the development of proxy-reported outcomes scales in other pediatric populations. |
format | Online Article Text |
id | pubmed-3161834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31618342011-08-26 Development of a proxy-reported pulmonary outcome scale for preterm infants with bronchopulmonary dysplasia Massie, Sara E Tolleson-Rinehart, Sue DeWalt, Darren A Laughon, Matthew M Powell, Leslie M Price, Wayne A Health Qual Life Outcomes Research BACKGROUND: To develop an accurate, proxy-reported bedside measurement tool for assessment of the severity of bronchopulmonary dysplasia (also called chronic lung disease) in preterm infants to supplement providers' current biometric measurements of the disease. METHODS: We adapted Patient-Reported Outcomes Measurement Information System (PROMIS) methodology to develop the Proxy-Reported Pulmonary Outcomes Scale (PRPOS). A multidisciplinary group of registered nurses, nurse practitioners, neonatologists, developmental specialists, and feeding specialists at five academic medical centers participated in the PRPOS development, which included five phases: (1) identification of domains, items, and responses; (2) item classification and selection using a modified Delphi process; (3) focus group exploration of items and response options; (4) cognitive interviews on a preliminary scale; and (5) final revision before field testing. RESULTS: Each phase of the process helped us to identify, classify, review, and revise possible domains, questions, and response options. The final items for field testing include 26 questions or observations that a nurse assesses before, during, and after routine care time and feeding. CONCLUSIONS: We successfully created a prototype scale using modified PROMIS methodology. This process can serve as a model for the development of proxy-reported outcomes scales in other pediatric populations. BioMed Central 2011-07-26 /pmc/articles/PMC3161834/ /pubmed/21791099 http://dx.doi.org/10.1186/1477-7525-9-55 Text en Copyright ©2011 Massie et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Massie, Sara E Tolleson-Rinehart, Sue DeWalt, Darren A Laughon, Matthew M Powell, Leslie M Price, Wayne A Development of a proxy-reported pulmonary outcome scale for preterm infants with bronchopulmonary dysplasia |
title | Development of a proxy-reported pulmonary outcome scale for preterm infants with bronchopulmonary dysplasia |
title_full | Development of a proxy-reported pulmonary outcome scale for preterm infants with bronchopulmonary dysplasia |
title_fullStr | Development of a proxy-reported pulmonary outcome scale for preterm infants with bronchopulmonary dysplasia |
title_full_unstemmed | Development of a proxy-reported pulmonary outcome scale for preterm infants with bronchopulmonary dysplasia |
title_short | Development of a proxy-reported pulmonary outcome scale for preterm infants with bronchopulmonary dysplasia |
title_sort | development of a proxy-reported pulmonary outcome scale for preterm infants with bronchopulmonary dysplasia |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161834/ https://www.ncbi.nlm.nih.gov/pubmed/21791099 http://dx.doi.org/10.1186/1477-7525-9-55 |
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