Airway clearance techniques for adults receiving extracorporeal membrane oxygenation for severe acute respiratory failure: a scoping review protocol
Tom Lunn, Ema Swingwood, Hannah Cochrane, Steven Walker, Fiona Cramp

TL;DR
This paper outlines a scoping review protocol to examine airway clearance techniques used in adult patients on ECMO for severe respiratory failure.
Contribution
The study introduces a systematic approach to map and synthesize evidence on airway clearance interventions in ECMO-treated adults.
Findings
The review will identify types of airway clearance interventions and their parameters.
It will assess physiological effects, outcomes, and safety of these interventions.
The findings aim to highlight practice variations and guide future research.
Abstract
Patients receiving extracorporeal membrane oxygenation (ECMO) for severe acute respiratory failure (SARF) often experience significant challenges with airway clearance due to disease severity, ultra-protective ventilation strategies and suppression of mucociliary and cough mechanisms. Extremely low tidal volumes and minimal flow rates further hinder secretion mobilisation. Despite increasing global use of ECMO, there is currently no synthesis of evidence describing airway clearance practices, their physiological rationale or outcomes in this population. This scoping review aims to explore the extent and nature of evidence on airway clearance interventions in invasively ventilated adult patients receiving ECMO for SARF. Specific objectives include mapping the types of interventions described and specific parameters, their intended physiological effects, reported outcomes and safety…
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
| Inclusion | Exclusion |
|---|---|
| Patients receiving airway clearance techniques | Children (<16 years old) |
| Adults (≥16 years old) | Patients supported solely by extracorporeal carbon dioxide removal |
| Patients receiving ECMO for severe acute respiratory failure | Patients exclusively receiving extracorporeal support for primary cardiac failure |
| Patients receiving invasive mechanical ventilation | |
| Any study design, including but not limited to: Controlled trials Before-and-after studies Interrupted time-series studies | |
| Additional sources of information: Expert opinion pieces Policies and guidelines Healthcare standards Technical reports Conference proceedings Published abstracts | |
| Published from 2000 onwards |
| Variable | Description of what will be documented |
|---|---|
| Authors | Full names of the authors of the included studies |
| Title | Full title of each included publication |
| Publication year | Year in which the study was published or made publicly available |
| Objective(s) | A description of the primary aim(s) or objective(s) |
| Study design (where relevant) | Methodological approach used (eg, RCT, observational study, case study) |
| Country | Country where the study was conducted/experts were based |
| Population characteristics | Description of the population, including demographics (eg, age, sex/gender), underlying pathology (eg, ARDS, asthma), type of ECMO used (eg, VV-ECMO, VA-ECMO) and type of invasive mechanical ventilation (if provided) |
| Intervention(s) and prescription details | Description of the intervention(s), including type, timing, frequency and duration |
| Rationale | Stated physiological rationale for use of intervention(s) |
| Clinician profession | Professional role of the individual(s) delivering the intervention (eg, physiotherapist, nurse, doctor). Staffing requirement for the delivered intervention (if provided) |
| Outcome evaluated | Outcome measures used to assess intervention effectiveness (eg, secretion volume, oxygenation indices, lung compliance) |
| Risks and safety considerations | Any risks, adverse effects or safety considerations reported in relation to the intervention |
- —http://dx.doi.org/10.13039/100015250NIHR Bristol Biomedical Research Centre
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Taxonomy
TopicsMechanical Circulatory Support Devices · Respiratory Support and Mechanisms · Tracheal and airway disorders
Background
Secretion clearance is a fundamental component of respiratory care in critically ill patients, and it presents distinct challenges in those receiving extracorporeal membrane oxygenation (ECMO) for severe acute respiratory failure (SARF). ECMO, in this setting, serves as an advanced life support modality that provides gas exchange for patients with SARF who are unresponsive to conventional mechanical ventilation.
In patients receiving ECMO, the combination of profound lung pathology, ultra-lung protective ventilation strategies, deep sedation and neuromuscular blockade significantly impairs normal airway clearance mechanisms, including mucociliary transport and the cough reflex.1 Impaired clearance can lead to lung volume loss, worsening ventilation-perfusion mismatch, atelectasis and increased susceptibility to ventilator-associated pneumonia (VAP), with secretion retention recognised as a key contributing factor to infection development.2 VAP is associated with increased mortality, prolonged mechanical ventilation and extended intensive care unit stays, making the prevention and management of secretion accumulation a priority in critical care.
Secretion clearance refers to the physiological and therapeutic processes aimed at mobilising and removing mucus and other airway secretions to maintain airway patency, optimise ventilation-perfusion matching and reduce the risk of infection. Under normal conditions, this process relies on an intact mucociliary escalator and effective cough reflex to transport secretions from the distal airways to the oropharynx for expectoration or swallowing. In mechanically ventilated patients, these mechanisms are frequently compromised, necessitating additional interventions. These may include lung hyperinflation, suctioning, patient positioning, manual techniques such as percussion and vibration, and the use of mucolytic agents.3 Each of these strategies aims to mobilise secretions, enhance the efficacy of airway suctioning and minimise associated complications.
While secretion management strategies are well established in mechanically ventilated patients with normal tidal volumes,3 these approaches have not been specifically evaluated in people receiving ECMO, where tidal volumes are frequently minimal, and respiratory mechanics are profoundly altered. ECMO use presents unique challenges, including the concept of the ‘baby lung’ (low functional lung capacity),4 heterogeneous time constants and the requirement to balance minimal ventilator settings with effective secretion clearance strategies. Traditional techniques for secretion mobilisation may not directly translate to this context, and interventions must be carefully adapted to avoid compromising lung protection or ECMO circuit dynamics.
To date, there is an absence of a comprehensive synthesis of the evidence regarding secretion clearance in people receiving invasive mechanical ventilation (IMV) and ECMO. Furthermore, there are no evidence-based national guidelines in the UK.
Objective
The primary objective of this review is to identify which airway clearance interventions are currently being used in patients receiving IMV and ECMO for SARF, how they are being applied, and the physiological and clinical rationales underpinning their use.
The scoping review will also aim to address the following secondary objectives:
What are the intervention parameters (eg, timing, dosage), and how do these align with different stages of the ECMO patient pathway?What outcomes are used to evaluate the effects of airway clearance interventions (eg, secretion volume, oxygenation indices, lung compliance, ventilation–perfusion matching, physiological response)?How are safety and adverse effects monitored and managed during airway clearance interventions?Which health professionals deliver the interventions, and what specific training or competencies are required (eg, physiotherapists, nurses, respiratory therapists, medical staff)?
Method
Study design
A scoping review was selected to address the study questions and is considered appropriate due to the complex evidence base including the potential heterogeneity of primary research data and need to map the extent, range and nature of available research rather than to answer a narrowly defined question.5 This methodology enables a comprehensive overview of existing research, highlights uncertainty and identifies priorities for future inquiry.
This scoping review will be conducted in accordance with the Joanna Briggs Institute (JBI) methodology for scoping reviews5 and reported in line with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews (PRISMA-ScR).6 Following this approach will help to ensure a rigorous, transparent and reproducible process for study selection, data extraction and synthesis.
Protocol and registration
This scoping review was registered on the Open Science Framework on the 1 September 2025 Unique identification number: osf.io/ptfr7
Patient and public involvement
Individuals with lived experience of intensive care, including those who had undergone ECMO, contributed to this review through a group patient and public involvement and engagement (PPIE) meeting. During the session, they endorsed the importance of the topic and helped refine the review focus. They will also be invited to provide feedback on the preliminary findings to support interpretation and dissemination.
Eligibility criteria
Inclusion criteria for the review were identified using the Population; Concept; Context framework for scoping reviews in accordance with the JBI methodology framework.5
Population
This scoping review will focus exclusively on the adult population receiving IMV and ECMO. Therefore, studies will be included only if the patient population is aged ≥16 years or where results are reported separately for adults.
Studies will be included if they focus on patients receiving ECMO for respiratory failure. This may encompass those initially managed with ultra-lung protective ventilation using very low tidal volumes, as well as patients in recovery phases marked by improving pulmonary compliance and the return of spontaneous ventilation. Studies exclusively involving patients receiving extracorporeal support for primary cardiac failure will be excluded, as they do not reflect the target population with primary respiratory pathology.
Paediatric studies will be excluded due to fundamental anatomical and physiological lung differences. These include smaller and more compliant airways, increased chest wall compliance, ongoing alveolar development, immature respiratory musculature and differing disease aetiology. These factors significantly alter respiratory pathophysiology and response to interventions, rendering findings in paediatric populations non-transferable to adults.
Studies involving patients supported solely by extracorporeal carbon dioxide removal (ECCO₂R) will also be excluded, as ECCO₂R is typically used in the context of isolated hypercapnic respiratory failure and does not reflect the population of interest.
Concept
This review will include studies that evaluate interventions aimed at airway clearance techniques in people receiving ECMO, delivered by clinicians from any professional discipline (eg, Physiotherapist, Nurse or Doctor).
Airway clearance refers to the mobilisation and removal of pulmonary secretions with the intent to improve respiratory mechanics, restore or maintain lung volumes and optimise ventilation-perfusion (V/Q) matching.
Interventions may include, but are not limited to, manual or mechanical physiotherapy techniques, suctioning methods, ventilator strategies, pharmacological adjuncts (eg, mucolytics), positioning approaches and bronchoscopy.
Context
This review will be situated within the context of severe respiratory failure managed in the critical care environment. Specifically, it will focus on patients receiving ECMO for life-threatening hypoxaemia. These clinical scenarios are frequently complicated by sepsis, cardiovascular instability and other factors that challenge the safe and effective delivery of routine respiratory care interventions.
Identifying relevant studies
The search strategy will aim to locate both published and unpublished studies via a three-step search strategy. First, an initial limited search of Embase (Ovid) and Google Scholar was undertaken to identify articles on the topic. The second component will be a comprehensive search strategy based on the text words contained in the titles and abstracts of relevant articles, and the index terms used to describe the articles. The draft search strategy for Embase (Ovid) was submitted for peer review by a second librarian in accordance with the Peer Review of Electronic Search Strategies guidelines.7 The peer-reviewed search strategy is provided as online supplemental additional file 1. This search strategy will be customised for each database, including MEDLINE (Ovid), Emcare (Ovid) and CINAHL (EBSCOhost). Step three will ensure searching of grey literature using a modified search strategy on TRIP and Google Scholar. We will consider search results from the first 10 pages of TRIP and Google Scholar for inclusion in the review. Inclusion and exclusion criteria are shown in table 1. Non-English language publications will be excluded due to resource limitations. Studies published in English from 2000 onwards will be included. A 25-year review period has been selected because the clinical use of ECMO for respiratory failure expanded substantially following the 2009 H1N1 influenza pandemic, which underscored ECMO’s efficacy in managing severe acute respiratory distress syndrome.
Selection of studies
Following the search, all identified citations will be collated and uploaded into Rayyan (a web-based review management platform) and duplicates removed. Titles and abstracts will be screened by two or more independent reviewers for assessment against the inclusion criteria for the review. Where one or more reviewers identify a citation as potentially relevant, sources will be retrieved and imported into Rayyan. The full text of selected citations will be assessed in detail against the inclusion criteria by two independent reviewers. Reasons for exclusion of sources of evidence at full text, that do not meet the inclusion criteria, will be recorded and reported in the scoping review. Any disagreements that arise between the reviewers at full text stage will be resolved through discussion, or with an additional reviewer.
Data charting process
Data will be extracted from sources included in the scoping review by two or more independent reviewers using a data extraction tool developed by the reviewers. The data extracted will include specific details about the participants, concept, context, study methods and key findings relevant to the review questions as per the JBI Manual of Evidence Synthesis V.10.2.7.5
The draft data extraction tool will be modified and revised during the process of extracting data from each included evidence source (see table 2). Modifications will be detailed in the scoping review. Any disagreements that arise between the reviewers will be resolved through discussion, or with an additional reviewer/s. If necessary, authors will be contacted to request missing or additional data.
Analysis and presentation of findings
The results of the search and the study inclusion process will be reported in full in the final scoping review and presented in a PRISMA flow diagram.8 Findings will be mapped by descriptive statistics (frequency counts) and presented using visualisation techniques (eg, tables, charts and/or figures) as appropriate. A narrative summary will accompany quantitative results. Basic qualitative content analysis will be conducted to identify key characteristics of the interventions used, plus the rationale, frequency, safety assessment and outcomes recorded. Reviewers will take an inductive approach to content analysis to allow better representation of these primary and secondary objectives of the scoping review.
Amendments
The study will adhere to the protocol as planned, with regular team-wide progress reviews. Any deviations or amendments made during the review will be documented and clearly reported in the final publication.
Ethics and dissemination
Ethical approval was not required as this study represents a protocol for a scoping review and does not involve human participants. Local research governance oversight and support were provided by the Research and Development Department, University Hospitals Bristol and Weston NHS Foundation Trust ([email protected]). Findings will be disseminated through publication in a peer-reviewed journal and presentation at relevant academic and professional meetings. The results are expected to highlight variations in practice and provide a foundation for future research aimed at optimising respiratory care and improving outcomes for patients receiving ECMO for SARF.
Supplementary material
10.1136/bmjopen-2025-111032online supplemental file 1
The reference list from the paper itself. Each links out to its DOI / PubMed record.
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- 5Aromataris E Lockwood C Porritt K et al JBI Manual for Evidence Synthesis JBI 2024
- 6Tricco AC Lillie E Zarin W et al PRISMA extension for scoping reviews (prisma-scr): checklist and explanation Ann Intern Med 20181694677310.7326/M 18-085030178033 · doi ↗ · pubmed ↗
- 7Mc Gowan J Sampson M Salzwedel DM et al PRESS peer review of electronic search strategies: 2015 guideline statement J Clin Epidemiol 20167540610.1016/j.jclinepi.2016.01.02127005575 · doi ↗ · pubmed ↗
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