Cardiac Resynchronization Therapy Pacing (CRT-P) - risk of loss of pacing therapy
Manufactured by Medtronic – battery voltage may reduce to a point where the device is no longer able to provide patient pacing therapy - MDA/2015/038
Action
- Identify all affected patients.
- Schedule an early follow up to discuss this issue with the patient, with priority given to pacing dependent patients.
- Compare the risk presented by device failure against that associated with device replacement on an individual patient basis. Patient assessment should include review of the: * degree of pacing-dependency * estimated remaining device longevity/time to ERI * applicability of the average mortality risk associated with device failure and device replacement, given by Medtronic (see background).
- Be aware that the low risk of device failure does not justify prophylactic replacement for the majority of non-pacing dependent patients.
- Repeat the above assessment at each follow-up appointment (intervals of 6 months or less).
- Remind patients to contact their follow-up centre if they experience increased symptoms of bradycardia or heart failure (including breathlessness) as this may be an indication of device failure.
Actions by
All cardiologists and cardiac physiologists who manage patients implanted with Cardiac Resynchronization Therapy Pacing devices
Deadlines for actions
Actions underway: 23 December 2015, actions complete: 9 June 2016
Device details
InSync III Models 8042U:
| Product description | Unique device identifier |
|---|---|
| IPG 8042U INSYNC III UNI INTL | 00613994322524 |
| IPG 8042U INSYNC III DC UNI EAME | 00681490993364 |
| IPG 8042U INSYNC III DC UNI EN/SV/DA | 00681490993388 |
| IPG 8042U INSYNC III DC UNI 5L | 00681490993395 |
| IPG 8042U INSYNC III DC UNI INTL | 00681490993425 |
Problem/background
Medtronic has identified that an unpredictable, but very small, subset of InSync III devices may develop unexpectedly high and variable battery impedances, which can reduce the battery voltage to a point where the current is insufficient to support pacing output. Reported harms to date include bradycardia, dyspnoea, complete heart block, weakness and dizziness. Medtronic has received one report of a patient death where it is possible, but unconfirmed, that this issue was a contributing factor.
There is no provocative testing that can predict which specific devices may fail, and there is no programming that can mitigate this issue. The failure results from the development of a resistive film on the cathode current collector. Development of the film is erratic and it is, therefore, not possible to identify a specific current drain above which the film will not develop and hence at which the devices are not at risk.
To date Medtronic has received 30 reports of devices affected by this issue, which represents 0.03% of those distributed worldwide, all of which have involved devices with implant duration over 53 months. Medtronic predicts the failure rate will be between 0.16% and 0.6% for the remaining active devices, with an associated mortality risk of 0.007-0.02%. This should be compared to Medtronic’s estimated average mortality risk presented by early device replacement of around 0.005%, although clearly this will vary significantly depending upon the patient circumstances.
Unfortunately the InSync III models are not supported by Medtronic’s Carelink network, and so it is not possible to review patients remotely.
In the UK nearly 6,000 potentially affected devices have been supplied between June 2001 and October 2010 when this product was discontinued, and therefore most devices can be expected to have exceeded 4 years implant duration. To date there have been two incidents associated with this problem reported within the UK.
Medtronic issued an FSN to affected hospitals on 10 November 2015 which includes patient management recommendations to mitigate the risk associated with this issue.
Manufacturer contacts
Manufacturer:
Keith Taverner
Medtronic Limited
Building 9, Hatters Lane
Croxley Green Business Park
Watford
WD18 8WW
Telephone: 01923 212 213
Email: [email protected]
Distribution
If you are responsible for cascading these alerts in your organisation, these are our suggested distribution lists.
Trusts (NHS boards in Scotland)
CAS and SABS (NI) liaison officers for onward distribution to all relevant staff including:
- A&E consultants
- A&E departments
- A&E directors
- A&E nurses
- adult intensive care units
- ambulance services directors
- ambulance staff
- anaesthesia, directors of
- anaesthetic medical staff
- anaesthetic nursing staff
- anaesthetists
- biomedical engineering staff
- biomedical science departments
- cardiac laboratory technicians
- cardiac pacing technicians
- cardiologists
- cardiology departments
- cardiology nurses
- cardiology, directors of
- cardiothoracic departments
- cardiothoracic surgeons
- cardiothoracic surgery directors
- clinical governance leads
- coronary care departments
- coronary care nurses
- EBME departments
- intensive care nursing staff (adult)
- intensive care units
- intensive care, directors of
- medical directors
- mri units, directors of
- nursing executive directors
- outpatient clinics
- outpatient theatre managers
- outpatient theatre nurses
- renal medicine departments
- renal medicine, directors of
- risk managers
- theatre managers
- theatre nurses
- theatres
Public Health England
Directors for onward distribution to:
- risk manager
NHS England area teams
CAS liaison officers for onward distribution to all relevant staff including:
- general practitioners
- general practice managers
Independent distribution
Establishments registered with the Care Quality Commission (CQC) (England only)
- hospitals in the independent sector
- independent treatment centres
- private medical practitioners
Establishments registered with OFSTED
- children’s services
- educational establishments with beds for children
- residential special schools
Please note: CQC and OFSTED do not distribute these alerts. Independent healthcare providers and social care providers can sign up to receive MDAs directly from the Department of Health’s Central Alerting System (CAS) by sending an email to: [email protected] and requesting this facility.
Enquiries
England
Send enquiries about this notice to MHRA, quoting reference number MDA/2015/038 or 2015/011/010/131/003.
Technical aspects
Feza Haque or Simon Holmes
MHRA
Telephone: 020 3080 7066 or 7240
Email: [email protected] or [email protected]
Clinical aspects
Dr Camilla Fleetcroft
MHRA
Telephone: 020 3080 6097
Email: [email protected]
Reporting adverse incidents in England
Northern Ireland
Alerts in Northern Ireland are distributed via the NI SABS system.
Enquiries and adverse incident reports in Northern Ireland should be addressed to:
Northern Ireland Adverse Incident Centre
CMO Group,
Department of Health, Social Services and Public Safety
Telephone: 028 9052 3868
Fax: 028 9052 3900
Email: [email protected]
Northern Ireland Adverse Incident Centre (NIAIC)
Reporting adverse incidents in Northern Ireland
Please report directly to NIAIC using the forms on our website.
Scotland
Enquiries and adverse incident reports in Scotland should be addressed to:
Incident Reporting and Investigation Centre
Health Facilities Scotland
NHS National Services Scotland
Telephone: 0131 275 7575
Fax: 0131 314 0722
Email: [email protected]
Reporting adverse incidents in Scotland
NHS Boards and Local Authorities in Scotland – report to Health Facilities Scotland.
Contractors such as private hospitals carrying out NHS work and private care homes that accept social work funded clients – report to Health Facilities Scotland.
Private facilities providing care to private clients report to the Care Inspectorate and MHRA.
Wales
Enquiries in Wales should be addressed to:
Healthcare Quality Division
Welsh Government
Telephone: 02920 823 624/02920 825 510
Email: [email protected]
Reporting adverse incidents in Wales
Report to MHRA through Yellow Card and follow specific advice for reporting in Wales in MDA/2004/054 (Wales).
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