TY - JOUR
T1 - Enzymatic therapy versus video-assisted thoracoscopic surgery for pleural infections
T2 - a systematic review and meta-analysis
AU - de Jonge, Weija R.
AU - Smits, Bo
AU - Ket, Johannes C. F.
AU - Altenburg, Josje
AU - Annema, Jouke
AU - Daniels, Johannes M. A.
AU - Dickhoff, Chris
AU - van Dorp, Martijn
AU - Braun, Jerry
AU - Korevaar, Daniel A.
AU - Heineman, David J.
N1 - Publisher Copyright:
© The authors 2025.
PY - 2025/3/1
Y1 - 2025/3/1
N2 - Aims Parapneumonic pleural infections are frequently encountered, but the optimal treatment regimen remains controversial. The aim of this systematic review was to investigate whether immediate video-assisted thoracoscopic surgery (VATS) has advantages over intrapleural enzymatic therapy (IET). Methods We searched MEDLINE, Embase and Web of Science Core Collection till November 2023 and included studies comparing IET and VATS in adult patients with parapneumonic pleural infections. Primary outcome was length of hospital stay (LOS); secondary outcomes included mortality and morbidity. Study quality was assessed using ROBINS-I and RoB 2. Inverse variance random-effects meta-analysis was performed. Results We screened 2263 articles; eight were included in the final analysis, covering 1023 patients (n=465 IET (mostly single agent IET); n=558 VATS). Six were non-randomised studies (n=5 with serious risk of bias) comprising 964 patients, and two were small, randomised feasibility studies (n=1 with high risk of bias), comprising 59 patients. In the meta-analysis, LOS in non-randomised studies was shorter for patients treated by VATS (mean difference 4.2 days; 95% CI 1.5–7.0). However, no significant difference was reported in the randomised feasibility studies. Mortality and morbidity rates showed no significant difference. Interpretation In this meta-analysis of non-randomised studies with a high risk of selection bias, VATS appears superior to IET regarding LOS in the treatment of parapneumonic pleural infections, without increased mortality and morbidity rate. Two recently published randomised feasibility studies failed to confirm this finding, but were not designed to detect a difference in LOS. This meta-analysis highlights the need for high-quality studies.
AB - Aims Parapneumonic pleural infections are frequently encountered, but the optimal treatment regimen remains controversial. The aim of this systematic review was to investigate whether immediate video-assisted thoracoscopic surgery (VATS) has advantages over intrapleural enzymatic therapy (IET). Methods We searched MEDLINE, Embase and Web of Science Core Collection till November 2023 and included studies comparing IET and VATS in adult patients with parapneumonic pleural infections. Primary outcome was length of hospital stay (LOS); secondary outcomes included mortality and morbidity. Study quality was assessed using ROBINS-I and RoB 2. Inverse variance random-effects meta-analysis was performed. Results We screened 2263 articles; eight were included in the final analysis, covering 1023 patients (n=465 IET (mostly single agent IET); n=558 VATS). Six were non-randomised studies (n=5 with serious risk of bias) comprising 964 patients, and two were small, randomised feasibility studies (n=1 with high risk of bias), comprising 59 patients. In the meta-analysis, LOS in non-randomised studies was shorter for patients treated by VATS (mean difference 4.2 days; 95% CI 1.5–7.0). However, no significant difference was reported in the randomised feasibility studies. Mortality and morbidity rates showed no significant difference. Interpretation In this meta-analysis of non-randomised studies with a high risk of selection bias, VATS appears superior to IET regarding LOS in the treatment of parapneumonic pleural infections, without increased mortality and morbidity rate. Two recently published randomised feasibility studies failed to confirm this finding, but were not designed to detect a difference in LOS. This meta-analysis highlights the need for high-quality studies.
UR - https://www.scopus.com/pages/publications/105008248359
U2 - 10.1183/23120541.00619-2024
DO - 10.1183/23120541.00619-2024
M3 - Article
C2 - 40040906
SN - 2044-6055
VL - 11
JO - ERJ Open Research
JF - ERJ Open Research
IS - 2
M1 - 00619-2024
ER -