Abstract

BackgroundThere is significant disparity between the respiratory health of Indigenous and non-Indigenous Australian infants. There is no culturally accepted measure to collect respiratory health outcomes in Indigenous infants. The aim of this study was to gain end user and expert consensus on the most relevant and acceptable respiratory and birth measures for Indigenous infants at birth, between birth and 6 months, and at 6 months of age follow-up for use in a research trial.MethodsA three round modified Delphi process was conducted from February 2018 to April 2019. Eight Indigenous panel members, and 18 Indigenous women participated. Items reached consensus if 7/8 (≥80%) panel members indicated the item was ‘very essential’. Qualitative responses by Indigenous women and the panel were used to modify the 6 months of age surveys.ResultsIn total, 15 items for birth, 48 items from 1 to 6 months, and five potential questionnaires for use at 6 months of age were considered. Of those, 15 measures for birth were accepted, i.e., gestational age, birth weight, Neonatal Intensive Care Unit (NICU) admissions, length, head circumference, sex, Apgar score, substance use, cord blood gas values, labour, birth type, health of the mother, number people living in the home, education of mother and place of residence. Seventeen measures from 1-to 6 months of age were accepted, i.e., acute respiratory symptoms (7), general health items (2), health care utilisation (6), exposure to tobacco smoke (1), and breastfeeding status (1). Three questionnaires for use at 6 months of age were accepted, i.e., a shortened 33-item respiratory questionnaire, a clinical history survey and a developmental questionnaire.ConclusionsIn a modified Delphi process with an Indigenous panel, measures and items were proposed for use to assess respiratory, birth and health economic outcomes in Indigenous Australian infants between birth and 6 months of age. This initial step can be used to develop a set of relevant and acceptable measures to report respiratory illness and birth outcomes in community based Indigenous infants.

Highlights

  • There is significant disparity between the respiratory health of Indigenous and non-Indigenous Australian infants

  • Participants were asked to indicate ‘yes’ or ‘no’ for inclusion of additional birth measures added by participants in round two (substance use in pregnancy, cord blood gas values, labour, birth type, health of mother, number people living in home, education and place of residence)

  • Key feedback on how the data should be collected included: a health professional should complete it with the woman and infant, the health professional must be familiar with working in Indigenous communities, and the questionnaire should be completed prior to a clinical assessment and the results provided to the clinical assessor

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Summary

Introduction

There is significant disparity between the respiratory health of Indigenous and non-Indigenous Australian infants. There is no culturally accepted measure to collect respiratory health outcomes in Indigenous infants. Indigenous Australian children experience unacceptably high rates of respiratory disease [1,2,3,4]. Rates of chronic respiratory disease are high among Indigenous children, including asthma (19.5%), bronchitis (16.8%), bronchiolitis (12.2%), pneumonia (7.2%) and bronchiectasis (1.5%) [6]. Poor respiratory health continues across the lifetime for Indigenous Australians leading to a shorter and poorer quality of life. Addressing the social determinants of health will see the greatest reduction in respiratory disease among Indigenous children, though clinical care must be improved simultaneously [2, 9]

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