GRAvity- versus Wall suction-drIven large volume Thoracentesis: a rAndomized controlled Study (GRAWITAS study).

complications pleural effusion suction thoracentesis

Journal

Chest
ISSN: 1931-3543
Titre abrégé: Chest
Pays: United States
ID NLM: 0231335

Informations de publication

Date de publication:
17 Jul 2024
Historique:
received: 12 12 2023
revised: 13 05 2024
accepted: 16 05 2024
medline: 20 7 2024
pubmed: 20 7 2024
entrez: 19 7 2024
Statut: aheadofprint

Résumé

Prior studies found no differences in procedural chest discomfort for patients undergoing manual syringe aspiration or drainage with gravity after thoracentesis. However, whether gravity drainage could protect against chest pain due to the larger negative pressure gradient generated by wall suction has not been investigated. Does wall suction drainage result in more chest discomfort compared to gravity drainage in patients undergoing large volume thoracentesis? In this multicenter, single-blinded, randomized controlled trial, patients with large free-flowing effusions of ≥500 mL were assigned to wall suction or gravity drainage in a 1:1 ratio. Wall suction was performed with suction system attached to the suction tubing and with vacuum pressure adjusted to full vacuum. Gravity drainage was performed with a drainage bag placed 100 cm below the catheter insertion site and connected via straight tubing. Patients rated chest discomfort on a 100-mm visual analog scale before, during, and after drainage. The primary outcome was postprocedural chest discomfort at 5 minutes. Secondary outcomes included measures of post procedure chest discomfort, breathlessness, procedure time, volume of fluid drained and complication rates. Of the 228 patients initially randomized, 221 were included in the final analysis. The primary outcome of procedural chest discomfort did not differ significantly between the groups (p = 0.08), nor did the secondary outcomes of postprocedural discomfort and dyspnea. Similar volumes were drained in both groups, but the procedure duration was longer in the gravity arm by approximately 3 minutes. No differences in rate of pneumothorax or re-expansion pulmonary edema were noted between the two groups. Thoracentesis via wall suction and gravity drainage results in similar levels of procedural discomfort and dyspnea improvement.

Sections du résumé

BACKGROUND BACKGROUND
Prior studies found no differences in procedural chest discomfort for patients undergoing manual syringe aspiration or drainage with gravity after thoracentesis. However, whether gravity drainage could protect against chest pain due to the larger negative pressure gradient generated by wall suction has not been investigated.
RESEARCH QUESTION OBJECTIVE
Does wall suction drainage result in more chest discomfort compared to gravity drainage in patients undergoing large volume thoracentesis?
STUDY DESIGN AND METHODS METHODS
In this multicenter, single-blinded, randomized controlled trial, patients with large free-flowing effusions of ≥500 mL were assigned to wall suction or gravity drainage in a 1:1 ratio. Wall suction was performed with suction system attached to the suction tubing and with vacuum pressure adjusted to full vacuum. Gravity drainage was performed with a drainage bag placed 100 cm below the catheter insertion site and connected via straight tubing. Patients rated chest discomfort on a 100-mm visual analog scale before, during, and after drainage. The primary outcome was postprocedural chest discomfort at 5 minutes. Secondary outcomes included measures of post procedure chest discomfort, breathlessness, procedure time, volume of fluid drained and complication rates.
RESULTS RESULTS
Of the 228 patients initially randomized, 221 were included in the final analysis. The primary outcome of procedural chest discomfort did not differ significantly between the groups (p = 0.08), nor did the secondary outcomes of postprocedural discomfort and dyspnea. Similar volumes were drained in both groups, but the procedure duration was longer in the gravity arm by approximately 3 minutes. No differences in rate of pneumothorax or re-expansion pulmonary edema were noted between the two groups.
INTERPRETATION CONCLUSIONS
Thoracentesis via wall suction and gravity drainage results in similar levels of procedural discomfort and dyspnea improvement.

Identifiants

pubmed: 39029784
pii: S0012-3692(24)04617-8
doi: 10.1016/j.chest.2024.05.046
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Samira Shojaee (S)

Division of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.

Jasleen Pannu (J)

Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, The Ohio State University Wexner Medical Center, Columbus, OH.

Lonny Yarmus (L)

Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.

Alberto Fantin (A)

Azienda Sanitaria Universitaria Friuli Centrale (AS UFC), Udine, Italy.

Christina MacRosty (C)

McKenzie Pulmonary Care Center, McKenzie-Willamette Medical Center, Springfield, OR.

Roland Bassett (R)

Biostatistics Department, The University of Texas MD Anderson Cancer Center, Houston, TX.

Labib Debiane (L)

Department of Medicine, Henry Ford Health System, Detroit, MI.

Zachary S DePew (ZS)

Division of Pulmonary, Critical Care, and Sleep Medicine, Creighton University, Omaha, NE.

Saadia A Faiz (SA)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Carlos A Jimenez (CA)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Sameer K Avasarala (SK)

University Hospitals, Case Western Reserve University School of Medicine, Cleveland, OH.

Erik Vakil (E)

University of Calgary, Calgary, Alberta, Canada.

Andrew DeMaio (A)

Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.

Lara Bashoura (L)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Keerthana Keshava (K)

New York-Presbyterian Brooklyn Methodist Hospital, Brooklyn, NY.

Travis Ferguson (T)

Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.

Roberto Adachi (R)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

George A Eapen (GA)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

David E Ost (DE)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Sami Bashour (S)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Asad Khan (A)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Vickie Shannon (V)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Ajay Sheshadri (A)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Roberto F Casal (RF)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Scott E Evans (SE)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Krystle Pew (K)

Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.

Nadia Castaldo (N)

Azienda Sanitaria Universitaria Friuli Centrale (AS UFC), Udine, Italy.

Diwakar D Balachandran (DD)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Vincenzo Patruno (V)

Azienda Sanitaria Universitaria Friuli Centrale (AS UFC), Udine, Italy.

Robert Lentz (R)

Division of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.

Cheryl Pai (C)

Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.

Fabien Maldonado (F)

Division of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.

Lance Roller (L)

Division of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.

Junsheng Ma (J)

Biostatistics Department, The University of Texas MD Anderson Cancer Center, Houston, TX.

Jhankruti Zaveri (J)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Jenna Los (J)

Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.

Luis Vaquero (L)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Eva Ordonez (E)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Gulmira Yermakhanova (G)

Division of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.

Jason Akulian (J)

Department of Pulmonary Medicine, University of North Carolina, North Carolina.

Cole Burks (C)

Department of Pulmonary Medicine, University of North Carolina, North Carolina.

Roel-Rolando Almario (RR)

Department of Medicine, Henry Ford Health System, Detroit, MI.

Marie Sauve (M)

Department of Medicine, Henry Ford Health System, Detroit, MI.

Jackson Pettee (J)

Department of Pulmonary Medicine, University of North Carolina, North Carolina.

Laila Z Noor (LZ)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Muhammad H Arain (MH)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Horiana B Grosu (HB)

Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX. Electronic address: hbgrosu@mdanderson.org.

Classifications MeSH