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Evaluating construct validity of the Asthma Impairment and Risk Questionnaire using a 3-month exacerbation recall.
Chipps, Bradley E; Murphy, Kevin R; Wise, Robert A; McCann, William A; Beuther, David A; Reibman, Joan; George, Maureen; Gilbert, Ileen; Eudicone, James M; Gandhi, Hitesh N; Harding, Gale; Ross, Melissa; Zeiger, Robert S.
Afiliação
  • Chipps BE; Capital Allergy & Respiratory Disease Center, Sacramento, California. Electronic address: BChipps@CapitalAllergy.com.
  • Murphy KR; Division of Allergy, Asthma and Immunology, Boys Town National Research Hospital, Boys Town, Nebraska.
  • Wise RA; Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • McCann WA; Allergy Partners, Asheville, North Carolina.
  • Beuther DA; Division of Pulmonary, Critical Care and Sleep Medicine, National Jewish Health, Denver, Colorado.
  • Reibman J; Department of Medicine, New York University School of Medicine, New York, New York.
  • George M; Department of Nursing, Columbia University School of Nursing, New York, New York.
  • Gilbert I; BioPharmaceuticals Medical, AstraZeneca, Wilmington, Delaware.
  • Eudicone JM; BioPharmaceuticals Medical, AstraZeneca, Wilmington, Delaware.
  • Gandhi HN; BioPharmaceuticals Medical, AstraZeneca, Wilmington, Delaware.
  • Harding G; Evidera, Bethesda, Maryland.
  • Ross M; Evidera, Bethesda, Maryland.
  • Zeiger RS; Departments of Allergy and Research and Evaluation, Kaiser Permanente Southern California, San Diego and Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, California.
Ann Allergy Asthma Immunol ; 128(5): 544-552.e3, 2022 05.
Article em En | MEDLINE | ID: mdl-35123077
ABSTRACT

BACKGROUND:

Recurrent assessment of asthma control is essential to evaluating disease stability and intervention impacts. An assessment that can be administered between annual clinic visits is needed. The Asthma Impairment and Risk Questionnaire (AIRQ) is a cross-sectionally validated, 10-item, yes or no, composite control tool evaluating previous 2-week symptoms and previous 12-month exacerbations.

OBJECTIVE:

To evaluate the construct validity of the AIRQ using a 3-month recall period for exacerbation-based risk questions and retaining the 2-week recall for symptom-based impairment items.

METHODS:

At baseline, patients completed the AIRQ with 12-month recall exacerbation items, Asthma Control Test (ACT), St. George's Respiratory Questionnaire (SGRQ), and global self-assessments of asthma risk, control, and symptom severity. Patient-reported exacerbations were captured monthly. The AIRQ with 3-month recall exacerbation items, ACT, and global self-assessments was administered at months 3, 6, and 9, and SGRQ at month 6.

RESULTS:

A total of 1112 patients aged 12 years or older were enrolled (mean [SD] age, 43.9 [19.5] years). The AIRQ and each administration of the AIRQ with 3-month recall exacerbation items classified asthma control similarly to an ACT plus exacerbation validation standard. For both AIRQ versions, SGRQ scores were higher with worsening asthma control (P < .001). At months 3, 6, and 9, worse AIRQ control levels were associated with higher proportions of patients with 1 or more and 2 or more exacerbations in the previous 3 months and patient global self-assessments indicating greater asthma morbidity (all P < .001).

CONCLUSION:

The AIRQ using exacerbation risk items with a 3-month recall period exhibits construct validity for classifying current asthma control and can be administered between annual AIRQ assessments.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma Tipo de estudo: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limite: Adult / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma Tipo de estudo: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limite: Adult / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article