Adaptive-Servo-Ventilation Therapy 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 ResMed Limited 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

안전성 경고는 의료기기 제품과 관련된 중요한 정보와 권고사항을 담고 있습니다. 물론 안전성 경고가 배포되었다고 해서 해당 제품이 무조건 안전하지 않은 제품이라는 것은 아닙니다. 보건의료업계 종사자와 의료기기 사용자들에게 배포되는 안전성 경고에는 회수(recall)도 포함될 수 있습니다. 제조사가 안전성 경고를 작성하기도 하지만, 보건당국에서 작성하는 경우도 있습니다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Safety alert
  • 날짜
    2015-05-14
  • 사례 출판 날짜
    2015-05-14
  • 사례 국가
  • 사례 출처
    DH
  • 사례 출처 URL
  • 비고 / 경고
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Hong Kong.
  • 데이터 추가 비고
    Medical Device Safety Alert
  • 원인
    Medical device safety alert: resmed adaptive-servo-ventilation therapy medicines and healthcare products regulatory agency (mhra), united kingdom, has issued a medical device safety alert concerning ventilators with adaptive servo-ventilation (asv), manufactured by resmed limited. the affected devices are identified as follows:- autoset cs, autoset cs pacewave, autoset cs2, autoset cs-a, vpap adapt, vpap adapt sv, vpap adapt sv-a, vpap tx, s9 autoset cs, s9 autoset cs pacewave, s9 autoset cs-a, s9 autoset cs-a pacewave, s9 vpap adapt, s9 vpap adapt easv, s9 vpap adapt pacewave, s9 vpap tx, aircurve 10 asv, aircurve 10 cs pacewave, lumis tx a serious safety concern has been identified during the preliminary primary data analysis from the serve-hf clinical trial. this trial investigated the effect of asv therapy on the hospitalisation and mortality rate of patients with symptomatic, chronic heart failure (nyha 2-4) with reduced left ventricular ejection fraction (lvef ≤ 45%) and moderate to severe predominant central sleep apnea (ahi ≥ 15/h, cahi/ahi ≥ 50% and cai ≥ 10/h). the identified safety concern is a significant increase in the risk of cardiovascular death in patients with symptomatic, chronic heart failure (nyha 2-4) with reduced left ventricular ejection fraction (lvef ≤ 45%) being treated with asv. mhra recommends affected users to take the following actions:- physicians managing patients with symptomatic chronic heart failure with reduced ejection fraction who are using resmed asv devices should contact their patients to discuss discontinuation of treatment. physicians should assess all patients currently being treated with asv mode for symptomatic chronic heart failure and if necessary undertake an assessment of lvef. where appropriate discontinuation of treatment needs to be discussed with patients physicians should be aware that new at risk patients should not use asv. asv therapy is now contraindicated in these at risk patients for details, please refer to the mhra websites:https://mhra.Filecamp.Com/public/file/28rq-imk5u9imhttps://www.Gov.Uk/drug-device-alerts/specific-resmed-ventilators-with-adaptive-servoventilation-asv-increased-risk-of-cardiovascular-death-in-patients-who-have-a-specific-heart-condition posted on 14 may 2015.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: ResMed Adaptive-Servo-Ventilation Therapy
  • Manufacturer

Manufacturer