Hypersensitivity pneumonitis - experiences in treatment so far and opening up new possibilities

Introduction/Objective. Hypersensitivity pneumonitis is a diagnostic and therapeutic challenge. It occurs due to an excessive immune response to inhaling an antigen (bacteria, fungi, or protozoa) to which the patient was previously sensitized. This study analyzes the clinical characteristics of patients during a 10-year period (2014?2023) treated at the Institute for Pulmonary Diseases of Vojvodina. Methods. A retrospective study was conducted including 74 patients. The first phase included data collection, the second phase included statistical data processing, and the third included the description of the obtained statistical parameters and discussion. Results. The average age was 57.61 ? 12.6 years; 52.7% were men, and 56.8% were non-smokers. Most patients had one or more comorbidities (70.3%). There were only 27 (36.5%) patients hospitalized more than three times. Progression and regression occurred in 14 (28%) patients each, while cessation occurred in 22 (44%). Fatal outcomes occurred in 7 (9.5%). It was determined that in patients with three or more comorbidities, ? 3 hospitalizations (9; 34.6%) occurred more often than < 3 hospitalizations (2; 4.2%) (Fisher?s exact test = 14.46; p = 0.04). By comparing the prognosis of the disease with the number of hospitalizations, we found a statistically significant association (Fisher?s exact test = 13.95; p = 0.001). The progression of the disease in patients with ? 3 hospitalizations (10; 62.5%) occurred more often than in patients with < 3 hospitalizations (4; 11.8%). Conclusion. To obtain adequate data on the success of therapy and its impact on slowing down the disease, further monitoring of patients who are on antifibrotic therapy is necessary.

Authors

Institutions

Publication Details

Journal
Srpski arhiv za celokupno lekarstvo
Published
2025-01-01
DOI
https://doi.org/10.2298/sarh250429063v
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Hypersensitivity pneumonitis - experiences in treatment so far and opening up new possibilities

Dragica Kovačević, Dejan Miljković, Emilija Vujičić, Jovan Javorac et al.
Srpski arhiv za celokupno lekarstvo
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
article

Hypersensitivity pneumonitis - experiences in treatment so far and opening up new possibilities

Dragica Kovačević, Dejan Miljković, Emilija Vujičić, Jovan Javorac, Miroslav Ilić, Dejan Živanović, Nevena Savić, Marina Kovač
article en

Abstract

Introduction/Objective. Hypersensitivity pneumonitis is a diagnostic and therapeutic challenge. It occurs due to an excessive immune response to inhaling an antigen (bacteria, fungi, or protozoa) to which the patient was previously sensitized. This study analyzes the clinical characteristics of patients during a 10-year period (2014?2023) treated at the Institute for Pulmonary Diseases of Vojvodina. Methods. A retrospective study was conducted including 74 patients. The first phase included data collection, the second phase included statistical data processing, and the third included the description of the obtained statistical parameters and discussion. Results. The average age was 57.61 ? 12.6 years; 52.7% were men, and 56.8% were non-smokers. Most patients had one or more comorbidities (70.3%). There were only 27 (36.5%) patients hospitalized more than three times. Progression and regression occurred in 14 (28%) patients each, while cessation occurred in 22 (44%). Fatal outcomes occurred in 7 (9.5%). It was determined that in patients with three or more comorbidities, ? 3 hospitalizations (9; 34.6%) occurred more often than < 3 hospitalizations (2; 4.2%) (Fisher?s exact test = 14.46; p = 0.04). By comparing the prognosis of the disease with the number of hospitalizations, we found a statistically significant association (Fisher?s exact test = 13.95; p = 0.001). The progression of the disease in patients with ? 3 hospitalizations (10; 62.5%) occurred more often than in patients with < 3 hospitalizations (4; 11.8%). Conclusion. To obtain adequate data on the success of therapy and its impact on slowing down the disease, further monitoring of patients who are on antifibrotic therapy is necessary.

Srpski arhiv za celokupno lekarstvoVol. 153(7-8)
University of Novi Sad (RS), Institute for Pulmonary Diseases of Vojvodina (RS)
Openalex Percentile: Top 71%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.