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N-Acetylcysteine Instillation During Bronchoscopy for Patients Requiring Non-Cystic Fibrosis-Related Mucus Secretion Clearance: A Review of Clinical Effectiveness and Guidelines

CADTH Rapid Response Report: Summary with Critical Appraisal

and .

Abbreviations

CRD

Centre for Reviews and Dissemination

MeSH

Medical Subject Headings

NAC

N-acetylcysteine

PRISMA

Preferred Reporting Items for Systematic Reviews and Meta-Analyses

Context and Policy Issues

Bronchoscopy is a commonly-used procedure that allows for the visualization of the lungs and air passages using a bronchoscope, a narrow tube with attached lighting and real-time video equipment.1 Bronchoscopy may be performed for several reasons, including the diagnosis of disease (e.g., lung cancer, tuberculosis, pneumonia, infections), foreign body removal, stent insertion, and biopsy.1,2 These procedures may be impeded in cases where the patient is experiencing impaired mucus secretion clearance as a result of various pathologies. Mucolytic agents (a class of drugs which aid in the clearance of mucus in the airways), such as N-acetylcysteine (NAC), may be administered prior to bronchoscopic examination in order to increase visibility and access to the underlying tissue.3,4 NAC’s mechanism of action involves the cleavage of disulfide bonds in heavily cross-linked mucus glycoproteins, resulting in decreased mucus viscosity, thereby facilitating its clearance.5,6

The purpose of the current report is to evaluate the clinical effectiveness and evidence-based guidelines regarding NAC instillation during bronchoscopy for non-cystic fibrosis patients requiring mucus secretion clearance. The findings of this review are complimented by two additional reports on the use of NAC in patients requiring mucus secretion clearance (not specific to bronchoscopy), conducted separately by CADTH.7,8

Research Questions

  1. What is comparative clinical effectiveness of N-acetylcysteine instillation versus saline (normal or hypertonic) during bronchoscopy for non-cystic fibrosis patients requiring mucus secretion clearance?
  2. What are the evidence-based guidelines for N-acetylcysteine instillation during bronchoscopy for non-cystic fibrosis patients requiring mucus secretion clearance?

Key Findings

No relevant literature was identified regarding the comparative clinical effectiveness of N-acetylcysteine instillation versus saline (normal or hypertonic) during bronchoscopy for non-cystic fibrosis patients requiring mucus secretion clearance. Additionally, no evidence-based guidelines were identified regarding N-acetylcysteine instillation during bronchoscopy for non-cystic fibrosis patients requiring mucus secretion clearance.

Methods

Literature Search Methods

A limited literature search was conducted by an information specialist on key resources including MEDLINE, Embase, the Cochrane Library, University of York Centre for Reviews and Dissemination (CRD) databases, Canadian and major international health technology agencies, as well as a focused Internet search. The search strategy was comprised of both controlled vocabulary, such as the National Library of Medicine’s MeSH (Medical Subject Headings), and keywords. The main search concepts were acetylcysteine and mucus or mucous secretions. No filters were applied to limit the retrieval by study type. The search was also limited to English language documents published between January 1, 2014 and July 8, 2019.

Selection Criteria and Methods

One reviewer screened citations and selected studies. In the first level of screening, titles and abstracts were reviewed and potentially relevant articles were retrieved and assessed for inclusion. The final selection of full-text articles was based on the inclusion criteria presented in Table 1.

Table 1. Selection Criteria.

Table 1

Selection Criteria.

Exclusion Criteria

Articles were excluded if they did not meet the selection criteria outlined in Table 1, they were duplicate publications, or were published prior to 2014. Guidelines with unclear methodology were also excluded.

Summary of Evidence

Quantity of Research Available

A total of 374 citations were identified in the literature search. Following screening of titles and abstracts, 359 citations were excluded and 15 potentially relevant reports from the electronic search were retrieved for full-text review. In addition, one potentially relevant publication was retrieved from the grey literature search for full-text review. Of these 16 potentially relevant articles, all were excluded for various reasons; no publications met the inclusion criteria and were included in this report. Appendix 1 presents the PRISMA9 flowchart of the study selection. References of potential interest are provided in Appendix 2.

Summary of Findings

No relevant literature was identified regarding NAC instillation during bronchoscopy for non-cystic fibrosis patients requiring mucus secretion clearance; therefore, no summary can be provided.

Limitations

No relevant literature was identified regarding the clinical effectiveness of NAC instillation versus saline (normal or hypertonic) during bronchoscopy for non-cystic fibrosis patients requiring mucus secretion clearance. Additionally, no evidence-based guidelines were identified regarding NAC instillation during bronchoscopy for non-cystic fibrosis patients requiring mucus secretion clearance. This report is limited by the timeframe used for literature searches (extended only to 2014); it is possible that relevant literature was published more than five years ago and was excluded by the current date-limited search.

Conclusions and Implications for Decision or Policy Making

No relevant literature or evidence-based guidelines were identified regarding NAC instillation during bronchoscopy for non-cystic fibrosis patients requiring mucus secretion clearance; therefore, no conclusions regarding the clinical effectiveness or evidence-based guidelines can be provided.

Research examining the comparative clinical effectiveness of NAC instillation during bronchoscopy for non-cystic fibrosis patients is required in order to investigate this potential application of NAC. The lack of published evidence precludes the creation of appropriate guidelines for health care providers who perform bronchoscopy in this patient population.

References

1.
Dumoulin E. Recent advances in bronchoscopy. F1000Research. 2018;7:1646. [PMC free article: PMC6192444] [PubMed: 30364219]
2.
Paradis TJ, Dixon J, Tieu BH. The role of bronchoscopy in the diagnosis of airway disease. J Thorac Dis. 2016;8(12):3826–3837. [PMC free article: PMC5227188] [PubMed: 28149583]
3.
Millman M, Goodman AH, Goldstein IM, Millman FM, Van Campen SS. Status Asthmaticus: use of acetylcysteine during bronchoscopy and lavage to remove mucous plugs. Ann Allergy. 1983;50(2):85–93. [PubMed: 6824202]
4.
Mata AF, Sarnaik AA. Bronchoscopy With N-Acetylcysteine Lavage in Severe Respiratory Failure From Pertussis Infection. Pediatrics. 2013;132(5):e1418–e1423. [PubMed: 24167177]
5.
Sathe NA, Krishnaswami S, Andrews J, Ficzere C, McPheeters ML. Pharmacologic Agents That Promote Airway Clearance in Hospitalized Subjects: A Systematic Review. Respir Care. 2015;60(7):1061–1070. [PubMed: 25944943]
6.
Aldini G, Altomare A, Baron G, et al. N-Acetylcysteine as an antioxidant and disulphide breaking agent: the reasons why. Free Radic Res. 2018;52(7):751–762. [PubMed: 29742938]
7.
Banerjee S, McCormack S. Acetylcysteine for patients requiring mucous secretion clearance: a review of clinical effectiveness and safety. (CADTH rapid response report: summary with critical appraisal). Ottawa (ON): CADTH; 2019: https://www​.cadth.ca​/sites/default/files​/pdf/htis/2019/RC1135​%20Acetylcysteine%20for​%20Secretions%20Final.pdf Accessed 2019 Jul 24. [PubMed: 31503431]
8.
Banerjee S, McCormack S. Acetylcysteine for patients requiring mucous secretion clearance: a review of guidelines.. (CADTH rapid response report: summary with critical appraisal). Ottawa (ON): CADTH; 2019: https://www​.cadth.ca​/sites/default/files​/pdf/htis/2019/RC1149​%20Acetylcysteine%20for​%20Secretions-Guidelines%20Final.pdf. Accessed 2019 Jul 24. [PubMed: 31503431]
9.
Liberati A, Altman DG, Tetzlaff J, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. J Clin Epidemiol. 2009;62(10):e1–e34. [PubMed: 19631507]

Appendix 1. Selection of Included Studies

Image app1f1

Appendix 2. Additional References of Potential Interest

Systematic Reviews and Meta-Analyses

    Alternative Population - Patients Not Undergoing Bronchoscopy

Review Articles

About the Series

CADTH Rapid Response Report: Summary with Critical Appraisal
ISSN: 1922-8147

Version: 1.0

Funding: CADTH receives funding from Canada’s federal, provincial, and territorial governments, with the exception of Quebec.

Suggested citation:

N-Acetylcysteine Instillation During Bronchoscopy for Patients Requiring Non-Cystic Fibrosis-Related Mucus Secretion Clearance: A Review of Clinical Effectiveness and Guidelines. Ottawa: CADTH; 2019 Aug. (CADTH rapid response report: summary with critical appraisal).

Disclaimer: The information in this document is intended to help Canadian health care decision-makers, health care professionals, health systems leaders, and policy-makers make well-informed decisions and thereby improve the quality of health care services. While patients and others may access this document, the document is made available for informational purposes only and no representations or warranties are made with respect to its fitness for any particular purpose. The information in this document should not be used as a substitute for professional medical advice or as a substitute for the application of clinical judgment in respect of the care of a particular patient or other professional judgment in any decision-making process. The Canadian Agency for Drugs and Technologies in Health (CADTH) does not endorse any information, drugs, therapies, treatments, products, processes, or services.

While care has been taken to ensure that the information prepared by CADTH in this document is accurate, complete, and up-to-date as at the applicable date the material was first published by CADTH, CADTH does not make any guarantees to that effect. CADTH does not guarantee and is not responsible for the quality, currency, propriety, accuracy, or reasonableness of any statements, information, or conclusions contained in any third-party materials used in preparing this document. The views and opinions of third parties published in this document do not necessarily state or reflect those of CADTH.

CADTH is not responsible for any errors, omissions, injury, loss, or damage arising from or relating to the use (or misuse) of any information, statements, or conclusions contained in or implied by the contents of this document or any of the source materials.

This document may contain links to third-party websites. CADTH does not have control over the content of such sites. Use of third-party sites is governed by the third-party website owners’ own terms and conditions set out for such sites. CADTH does not make any guarantee with respect to any information contained on such third-party sites and CADTH is not responsible for any injury, loss, or damage suffered as a result of using such third-party sites. CADTH has no responsibility for the collection, use, and disclosure of personal information by third-party sites.

Subject to the aforementioned limitations, the views expressed herein are those of CADTH and do not necessarily represent the views of Canada’s federal, provincial, or territorial governments or any third party supplier of information.

This document is prepared and intended for use in the context of the Canadian health care system. The use of this document outside of Canada is done so at the user’s own risk.

This disclaimer and any questions or matters of any nature arising from or relating to the content or use (or misuse) of this document will be governed by and interpreted in accordance with the laws of the Province of Ontario and the laws of Canada applicable therein, and all proceedings shall be subject to the exclusive jurisdiction of the courts of the Province of Ontario, Canada.

Copyright © 2019 Canadian Agency for Drugs and Technologies in Health.

The copyright and other intellectual property rights in this document are owned by CADTH and its licensors. These rights are protected by the Canadian Copyright Act and other national and international laws and agreements. Users are permitted to make copies of this document for non-commercial purposes only, provided it is not modified when reproduced and appropriate credit is given to CADTH and its licensors.

Except where otherwise noted, this work is distributed under the terms of a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International licence (CC BY-NC-ND), a copy of which is available at http://creativecommons.org/licenses/by-nc-nd/4.0/

Bookshelf ID: NBK549208PMID: 31682390

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