Complicated Pleural Infection is Associated With Prolonged Recovery and Reduced Functional Ability.


Journal

Journal of bronchology & interventional pulmonology
ISSN: 1948-8270
Titre abrégé: J Bronchology Interv Pulmonol
Pays: United States
ID NLM: 101496866

Informations de publication

Date de publication:
01 Oct 2024
Historique:
received: 17 01 2024
accepted: 24 05 2024
medline: 22 7 2024
pubmed: 22 7 2024
entrez: 22 7 2024
Statut: epublish

Résumé

Management of complicated pleural infections (CPIs) had historically been surgical; however, following the publication of the second multicenter intrapleural sepsis trial (MIST-2), combination tissue plasminogen (tPA) and dornase (DNase) offers a less invasive and effective treatment. Our aim was to assess the quality of life (QOL) and functional ability of patients' recovery from a CPI managed with either intrapleural fibrinolytic therapy (IPFT) or surgery. We identified 565 patients managed for a CPI between January 1, 2013 and March 31, 2018. There were 460 patients eligible for contact, attempted through 2 phone calls and one mailer. Two questionnaires were administered: the Short Form 36-Item Health Survey (SF-36) and a functional ability questionnaire. Contact was made in 35% (159/460) of patients, and 57% (90/159) completed the survey. Patients had lower QOL scores compared to average US citizens; those managed with surgery had higher scores in physical functioning (surgery: 80, IPFT: 70, P=0.040) but lower pain scores (surgery: 58, IPFT: 68, P=0.045). Of 52 patients who returned to work, 48% (25) reported an impact on their work effectiveness during recovery, similarly between management strategies (IPFT: 50%, 13/26 vs. surgery: 46%, 12/26; P=0.781). Patients with a CPI had a lower QOL compared with average US citizens. Surgically managed patients reported improved physical functioning but worse pain compared with patients managed with IPFT. Patients returned to work within 4 weeks of discharge, and nearly half reported their ability to work effectively was impacted by their recovery. With further research into recovery timelines, patients may be appropriately counselled for expectations.

Sections du résumé

BACKGROUND BACKGROUND
Management of complicated pleural infections (CPIs) had historically been surgical; however, following the publication of the second multicenter intrapleural sepsis trial (MIST-2), combination tissue plasminogen (tPA) and dornase (DNase) offers a less invasive and effective treatment. Our aim was to assess the quality of life (QOL) and functional ability of patients' recovery from a CPI managed with either intrapleural fibrinolytic therapy (IPFT) or surgery.
METHODS METHODS
We identified 565 patients managed for a CPI between January 1, 2013 and March 31, 2018. There were 460 patients eligible for contact, attempted through 2 phone calls and one mailer. Two questionnaires were administered: the Short Form 36-Item Health Survey (SF-36) and a functional ability questionnaire.
RESULTS RESULTS
Contact was made in 35% (159/460) of patients, and 57% (90/159) completed the survey. Patients had lower QOL scores compared to average US citizens; those managed with surgery had higher scores in physical functioning (surgery: 80, IPFT: 70, P=0.040) but lower pain scores (surgery: 58, IPFT: 68, P=0.045). Of 52 patients who returned to work, 48% (25) reported an impact on their work effectiveness during recovery, similarly between management strategies (IPFT: 50%, 13/26 vs. surgery: 46%, 12/26; P=0.781).
CONCLUSION CONCLUSIONS
Patients with a CPI had a lower QOL compared with average US citizens. Surgically managed patients reported improved physical functioning but worse pain compared with patients managed with IPFT. Patients returned to work within 4 weeks of discharge, and nearly half reported their ability to work effectively was impacted by their recovery. With further research into recovery timelines, patients may be appropriately counselled for expectations.

Identifiants

pubmed: 39037060
doi: 10.1097/LBR.0000000000000974
pii: 01436970-202410010-00001
pii:
doi:

Substances chimiques

Tissue Plasminogen Activator EC 3.4.21.68
Fibrinolytic Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

Disclosure: There is no conflict of interest or other disclosures.

Références

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Auteurs

Austin M Meggyesy (AM)

Division of Thoracic Surgery and Interventional Pulmonology, Swedish Cancer Institute, Seattle, WA.

Candice L Wilshire (CL)

Division of Thoracic Surgery and Interventional Pulmonology, Swedish Cancer Institute, Seattle, WA.

Adam J Bograd (AJ)

Division of Thoracic Surgery and Interventional Pulmonology, Swedish Cancer Institute, Seattle, WA.

Shih Ting Chiu (ST)

Medical Data Research Center, Providence Health and Services, Portland, OR.

Christopher R Gilbert (CR)

Division of Thoracic Surgery and Interventional Pulmonology, Swedish Cancer Institute, Seattle, WA.

Najib M Rahman (NM)

NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.

Eihab O Bedawi (EO)

NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.

Eric Vallieres (E)

Division of Thoracic Surgery and Interventional Pulmonology, Swedish Cancer Institute, Seattle, WA.

Jed A Gorden (JA)

Division of Thoracic Surgery and Interventional Pulmonology, Swedish Cancer Institute, Seattle, WA.

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Classifications MeSH