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Ventilator change in children on home mechanical ventilation affected by the Philips respironics trilogy ventilator
Heather Brandt1, Dawn M Simon1, Ajay S Kasi1
1Division of Pediatric Pulmonology, Department of Pediatrics, Children's Healthcare of Atlanta, Emory University, Atlanta, Georgia, USA.
Insights
The Philips Respironics recall impacted Trilogy ventilators used in children requiring home positive airway pressure ventilation via tracheostomy (PPV-T). A collaborative protocol helped transition these patients to new portable home ventilators (PHV) efficiently.
Area of Science:
- Pediatric Respiratory Care
- Medical Device Recalls
- Home Ventilation
Background:
- The 2021 Philips Respironics recall affected Trilogy ventilators crucial for pediatric home positive airway pressure ventilation via tracheostomy (PPV-T).
- Optimal strategies for replacing recalled ventilators in this vulnerable population were unclear.
Purpose of the Study:
- To evaluate the effectiveness of a collaborative institutional protocol for transitioning children using recalled Trilogy ventilators to non-recalled portable home ventilators (PHV).
Main Methods:
- Retrospective study of children with recalled Trilogy ventilators requiring home PPV-T.
- Analysis of patients who underwent inpatient ventilator change to PHV using a collaborative protocol.
- Data collected on hospitalization duration for ventilator change.
Main Results:
- 19 children transitioned from recalled Trilogy ventilators to PHV during the study period.
- The median hospitalization duration for ventilator change was 2 days (IQR: 6 days).
- Patients admitted solely for ventilator change had a median hospitalization of 1 day.
Conclusions:
- A systematic, collaborative protocol involving patients, physicians, and durable medical equipment companies can optimize the transition to non-recalled portable home ventilators for children.
- This approach addresses critical needs following significant medical device recalls in pediatric home ventilation.
Abstract:
The Philips Respironics recall notification issued in June 2021 affected many of their positive airway pressure devices and mechanical ventilators including the Trilogy 100 and 200 ventilators that are often utilized in children using home positive pressure ventilation via tracheostomy (PPV-T). Optimal strategies to replace ventilators in children using home PPV-T affected by the Philips recall are unknown. We conducted a retrospective study of children using home PPV-T with recalled Trilogy ventilators who underwent inpatient ventilator change to non-recalled portable home ventilators (PHV) using our collaborative institutional protocol. During the study period, there were 40 children using PPV-T with recalled Trilogy ventilators and 19 patients underwent inpatient ventilator change either during an elective hospitalization (n = 8) or during an unscheduled or postoperative hospitalization (n = 11). The median duration of hospitalization for ventilator change was 2 days (interquartile range: 6 days) and generally 1 day for patients admitted solely for ventilator change. In children using PPV-T with recalled Trilogy ventilators, a systematic protocol collaborating with the patients, physicians, and durable medical equipment companies may optimize transition to nonrecalled PHVs.
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