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Risk factors and prevention strategies for medical device-related pressure injuries in critically ill patientsNew research identifies key risks for medical device pressure injuries

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Key Takeaway
Note that risk factors and prevention for MDRPIs involve device, patient, and care-related categories.

This scoping review examines the characteristics, risk factors, and prevention measures associated with medical device-related pressure injuries (MDRPIs) in critically ill patients. The review synthesizes data from a sample of 15,341 patients to identify common clinical patterns and management strategies.

Key findings indicate that responsible medical devices for these injuries include endotracheal, orotracheal, and nasotracheal intubation tubes. The most commonly affected anatomical locations involve the nose, nasal mucosa, mouth, lips, and ear. Risk factors are categorized into three distinct domains: medical devices, patient-specific factors, and treatment- and care-related factors.

Preventative and nursing measures are similarly categorized into medical devices, patient-specific factors, and treatment- and care-related factors. Core interventions for managing MDRPIs include risk assessment, device optimization, positioning management, and skin care. The review identifies these categories of risk factors and interventions rather than specific statistical associations between individual factors and outcomes. Clinical application of these findings focuses on standardizing nursing protocols and device management in intensive care settings.

How this fits prior evidence

This scoping review addresses a gap in the systematic categorization of risk factors and nursing interventions for medical device-related pressure injuries (MDRPIs) in critically ill patients. While prior coverage noted very uncertain evidence for CO therapy in wound healing, this review focuses on the specific management of injuries caused by medical devices such as intubation tubes.

When patients are critically ill, they often rely on life-saving equipment like breathing tubes. However, these devices can cause painful and serious skin damage known as medical device-related pressure injuries. This type of injury is particularly common in areas like the nose, mouth, lips, and ears.

A review of over 15,000 cases helped map out what causes these injuries. Researchers found that risks fall into three main buckets: the specific medical devices used, factors unique to the patient, and the way care is delivered. Identifying these factors helps teams focus on where the most danger lies.

To keep patients safe, the review highlights four main areas of focus: risk assessment, optimizing the devices used, managing how patients are positioned, and consistent skin care. These steps are essential for protecting the skin of patients who are too ill to move or speak for themselves.

What this means for you:
Care teams can reduce skin damage from medical devices by focusing on risk assessment, device optimization, and skin care.

Common questions

What are medical device-related pressure injuries?

These are injuries to the skin caused by medical equipment. In this review of 15,341 cases, the most common areas affected were the nose, nasal mucosa, mouth, lips, and ear. These injuries often happen to critically ill patients who require tubes for breathing or other life-saving treatments.

What factors increase the risk of these injuries?

Risk factors for these injuries are grouped into three categories: the specific medical devices used, factors unique to the patient, and factors related to the treatment and care provided. Identifying these helps medical teams better protect the skin of patients in critical care.

How can medical teams prevent these injuries?

There are four core ways to prevent these injuries: risk assessment, device optimization, positioning management, and skin care. These measures are essential for protecting patients from damage caused by items like endotracheal, orotracheal, or nasotracheal intubation tubes.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedAug 2026
View Original Abstract ↓
BackgroundStudies on medical device-related pressure injuries (MDRPIs) in critically ill patients still face some nonnegligible challenges, impeding the development and implementation of evidence-based interventions.ObjectivesThe purpose of this review is to investigate MDRPIs in critically ill patients, from the aspects of characteristics, risk factors, prevention and nursing measures, to improve high-quality assessment, treatment, and management of critically ill patients with MDRPIs.MethodsA systematic literature search was conducted across major electronic databases to identify relevant studies. In addition, the websites and materials from relevant associations, professional organizations, and official departments were also searched for further information. Necessary manual search for references of the retrieved articles was performed to capture potential eligible studies. Two reviewers independently conducted study selection based on the inclusion and exclusion criteria, and then data extraction was carried out by using a pre-designed form. A comprehensive summary of the findings from the final included studies in relation to MDRPIs in critically ill patients was achieved through narrative data synthesis.ResultsEighteen articles were finally included, which were conducted in Brazil, Australia, New Zealand, Turkey, Norway, Jordan, and China, respectively, covering 15,341 critically ill patients. Various medical devices are responsible for MDRPIs in critically ill patients, mainly including endotracheal/orotracheal/nasotracheal intubation tubes. The most commonly affected anatomical locations involving the nose/nasal mucosa, mouth, lips, and ear. The MDRPIs in critically ill patients are caused by the interaction of multiple factors, which can be generally classified into three categories: medical devices, patient-specific factors, and treatment- and care-related factors. Correspondingly, the synthesized preventative and nursing measures were also categorized into the abovementioned three categories.ConclusionMDRPIs exhibit device-dependent injury characteristics, with risk factors involving multi-dimensional interactions among medical devices, patients, and treatment and care procedures. Risk assessment, device optimization, positioning management, and skin care are core interventions for the occurrence of MDRPIs in critically ill patients. In order to provide safe and effective treatment and care services for critically ill patients, the prevention and control of MDRPIs should be guided by existing evidence, integrate innovative technologies and practical wisdom, improve the professional competence of medical staff, and enhance multidisciplinary collaboration.
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