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Assessment and monitoring of lung disease in patients with severe alpha 1 antitrypsin deficiency: a european delphi consensus of the EARCO group.
Miravitlles, Marc; Turner, Alice M; Sucena, Maria; Mornex, Jean-François; Greulich, Timm; Wencker, Marion; McElvaney, N Gerard.
Afiliação
  • Miravitlles M; Pneumology Department, Health Care Provider of the European Reference Network On Rare Respiratory Diseases (ERN LUNG), Hospital Universitari Vall d'Hebron/Vall d'Hebron Research Institute (VHIR), Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain. marcm@separ.es.
  • Turner AM; Institute of Applied Health Research, University of Birmingham, Birmingham, UK.
  • Sucena M; University Hospitals Birmingham, Birmingham, UK.
  • Mornex JF; Pulmonology Department, Centro Hospitalar Universitário de Santo António, Porto, Portugal.
  • Greulich T; Université Claude Bernard Lyon 1, INRAE, UMR754, IVPC, Hospices Civils de Lyon, Inserm, CIC1407, F-69100, Lyon, France.
  • Wencker M; Department of Medicine, Pulmonary and Critical Care Medicine, Member of the German Center for Lung Research (DZL), University Medical Center Giessen and Marburg, Philipps-University, Marburg, Germany.
  • McElvaney NG; Conresp, Loerzweiler, Germany.
Respir Res ; 25(1): 318, 2024 Aug 19.
Article em En | MEDLINE | ID: mdl-39160517
ABSTRACT

BACKGROUND:

Currently, there is conflicting information and guidance on the effective management of Alpha 1 Antitrypsin Deficiency (AATD). Establishing a consensus of assessment and disease management specific to AATD is important for achieving a standardized treatment pathway and for improving patient outcomes. Here, we aim to utilize the Delphi method to establish a European consensus for the assessment and management of patients with severe AATD.

METHODS:

Two rounds of a Delphi survey were completed online by members of the European Alpha-1 Research Collaboration (EARCO). Respondents were asked to indicate their agreement with proposed statements for patients with no respiratory symptoms, stable respiratory disease, and worsening respiratory disease using a Likert scale of 1-7. Levels of agreement between respondents were calculated using a weighted average.

RESULTS:

Round 1 of the Delphi survey was sent to 103 members of EARCO and 38/103 (36.9%) pulmonologists from across 15 countries completed all 109 questions. Round 2 was sent to all who completed Round 1 and 36/38 (94.7%) completed all 79 questions. Responses regarding spirometry, body plethysmography, high-resolution computed tomography, and the initiation of augmentation therapy showed little variability among physicians, but there was discordance among other aspects, such as the use of low-dose computed tomography in both a research setting and routine clinical care.

CONCLUSIONS:

These results provide expert opinions for the assessment and monitoring of patients with severe AATD, which could be used to provide updated recommendations and standardized treatment pathways for patients across Europe.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Técnica Delphi / Deficiência de alfa 1-Antitripsina / Consenso Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Técnica Delphi / Deficiência de alfa 1-Antitripsina / Consenso Idioma: En Ano de publicação: 2024 Tipo de documento: Article