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Treatment and management of primary antibody deficiency: German interdisciplinary evidence���based consensus guideline

Authors :
Jana Pachlopnik-Schmid
Kirsten Wittke
Horst von Bernuth
Rainer Müller
Klaus Warnatz
Fabian Hauck
Pirmin Habermehl
Leif G. Hanitsch
Claudia Wehr
Gerd Klock
Ulrike Burkhard-Meier
Kaan Boztug
Ulrich Baumann
Maria Fasshauer
Oliver Meyer
Dorothea Pfeiffer-Kascha
Johannes G. Liese
Tim Niehues
University of Zurich
Hanitsch, Leif
Publication Year :
2020
Publisher :
Charit�� - Universit��tsmedizin Berlin, 2020.

Abstract

This evidence‐based clinical guideline provides consensus‐recommendations for the treatment and care of patients with primary antibody deficiencies (PADs). The guideline group comprised 20 clinical and scientific expert associations of the German, Swiss, and Austrian healthcare system and representatives of patients. Recommendations were based on results of a systematic literature search, data extraction, and evaluation of methodology and study quality in combination with the clinical expertise of the respective representatives. Consensus‐based recommendations were determined via nominal group technique. PADs are the largest clinically relevant group of primary immunodeficiencies. Most patients with PADs present with increased susceptibility to infections, however immune dysregulation, autoimmunity, and cancer affect a significant number of patients and may precede infections. This guideline therefore covers interdisciplinary clinical and therapeutic aspects of infectious (e.g., antibiotic prophylaxis, management of bronchiectasis) and non‐infectious manifestations (e.g., management of granulomatous disease, immune cytopenia). PADs are grouped into disease entities with definitive, probable, possible, or unlikely benefit of IgG‐replacement therapy. Summary and consensus‐recommendations are provided for treatment indication, dosing, routes of administration, and adverse events of IgG‐replacement therapy. Special aspects of concomitant impaired T‐cell function are highlighted as well as clinical data on selected monogenetic inborn errors of immunity formerly classified into PADs (APDS, CTLA‐4‐, and LRBA‐deficiency).

Details

Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....7d38bc4b6224e82f4d7403393c82cbed
Full Text :
https://doi.org/10.17169/refubium-33689