cardiac implantable device nice

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Cardiac resynchronisation therapy for the treatment of heart failure 1 Guidance This guidance should be read in conjunction with ‘Implantable cardioverter defibrillators for arrhythmias’ (NICE technology appraisal guidance 95; see www.nice.org.uk/TA095). This guidance on cardiac resynchr onisation therapy provides additional treatment options for some of the groups of people covered in the guidance on implantable cardioverter defibrillators (ICDs). 1.1 Ca rd iac re sy nc hr onisation therapy wi th a pa ci ng device (CRT-P) is recommended as a treatment option for people with heart failure who fulfil all the following criteria. The y are current ly ex periencin g or ha ve recently experienced New York Heart Association (NYHA) class III–IV symptoms. They a re in si nu s rh yt hm: either with a QRS duration of 150 ms or longer estimated by standard electrocardi ogram (ECG) or with a QRS duration of 120–149 ms estimated by ECG and mechanical dyssynchr ony that is confirmed by echocardiography. They have a le ft ve ntric ular ejection fracti on o f 35% or less. They are receiving optimal pharmacolo gica l therapy. 1.2 Ca rd iac res yn ch ronisa ti on th er ap y wit h a defibrillator device (CRT-D) may be considered for people who fulfil the criteria for implantation of a CRT-P device in section 1.1 and who also separately fulfil the criteria for the use of an ICD device as recommended in NICE technology appraisal guidance 95. 2 Implementation NICE has developed tools to help organisations implemen t this guidance (listed below). These are available on our website (www.nice.org.uk/TA120). Loca l cos ting templ ate in corporating co sting report to estimate the savings and costs associated with implementation. Audit c rit eria to monit or local p rac tic e. NICE technology appraisal guidance 120 This guidance is written in the following context This guidance represents the view of the Institute, which was arrived at after careful consideration of the available evidence. Healthcare professionals are expected to take it fully into account when exercising their clinical judgement. This guidance does not, however, override the individual responsibility of healthcare professionals to make appropriate decisions in the circumstances of the individual patient, in consultation with the patient and/or guardian or carer. Issue date: May 2007 Review date: July 2010 1 Quick reference guide NHS National Institute for Health and Clinical Excellence 1 The guidance on this technology for people who do not have additional risk factors for sudden cardiac death will be considered for review in July 2010. Guidance on the use of a defibrillator device (CRT-D or ICD) for people with heart failure and additional risk factors for sudden cardiac death will be considered for review in 2008.

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8/3/2019 Cardiac Implantable Device NICE

http://slidepdf.com/reader/full/cardiac-implantable-device-nice 1/2

Cardiac resynchronisation therapy for thetreatment of heart failure

1 Guidance

This guidance should be read in conjunction with‘Implantable cardioverter defibrillators for arrhythmias’(NICE technology appraisal guidance 95; see

www.nice.org.uk/TA095). This guidance on cardiacresynchronisation therapy provides additional treatmentoptions for some of the groups of people covered in theguidance on implantable cardioverter defibrillators (ICDs).

1.1 Cardiac resynchronisation therapy with a pacingdevice (CRT-P) is recommended as a treatmentoption for people with heart failure who fulfil allthe following criteria.

• They are currently experiencing or haverecently experienced New York HeartAssociation (NYHA) class III–IV symptoms.

• They are in sinus rhythm:– either with a QRS duration of 150 ms or

longer estimated by standardelectrocardiogram (ECG)

– or with a QRS duration of 120–149 msestimated by ECG and mechanicaldyssynchrony that is confirmed byechocardiography.

• They have a left ventricular ejection fraction of35% or less.

• They are receiving optimal pharmacological

therapy.

1.2 Cardiac resynchronisation therapy with adefibrillator device (CRT-D) may be considered forpeople who fulfil the criteria for implantation of a

CRT-P device in section 1.1 and who alsoseparately fulfil the criteria for the use of an ICDdevice as recommended in NICE technologyappraisal guidance 95.

2 Implementation

NICE has developed tools to help organisations implementthis guidance (listed below). These are available on ourwebsite (www.nice.org.uk/TA120).

• Local costing template incorporating costing report toestimate the savings and costs associated with

implementation.

• Audit criteria to monitor local practice.

NICE technology appraisal guidance 120This guidance is written in the following context

This guidance represents the view of the Institute, which was arrived at after careful consideration of the availableevidence. Healthcare professionals are expected to take it fully into account when exercising their clinical judgement.This guidance does not, however, override the individual responsibility of healthcare professionals to make appropriatedecisions in the circumstances of the individual patient, in consultation with the patient and/or guardian or carer.

Issue date: May 2007

Review date: July 20101

Quick reference guide

NHS National Institute for 

Health and Clinical Excellence

1 The guidance on this technology for people who do not have additional risk factors for sudden cardiac death will be considered forreview in July 2010. Guidance on the use of a defibrillator device (CRT-D or ICD) for people with heart failure and additional riskfactors for sudden cardiac death will be considered for review in 2008.

8/3/2019 Cardiac Implantable Device NICE

http://slidepdf.com/reader/full/cardiac-implantable-device-nice 2/2

Further information

Quick reference guide

This has been distributed to healthcare professionalsworking in the NHS in England and Wales (seewww.nice.org.uk/TA120distributionlist). It is available fromwww.nice.org.uk/TA120quickrefguide

For printed copies, phone the NHS Response Line on0870 1555 455 (quote reference number N1265).

Full guidance

This contains the following sections:

1 Guidance

2 Clinical need and practice

3 The technology

4 Evidence and interpretation

5 Implementation

6 Recommendations for further research

7 Related NICE guidance

8 Review of guidance.

The full guidance also gives details of the AppraisalCommittee and the sources of evidence considered. It isavailable from www.nice.org.uk/TA120guidance

‘Understanding NICE guidance’

Information for patients and their carers is available fromwww.nice.org.uk/TA120publicinfo

For printed copies, phone the NHS Response Line on0870 1555 455 (quote reference number N1266).

Related NICE guidance

• MI: secondary prevention in primary and secondarycare for patients following a myocardial infarction.NICE clinical guideline 48 (2007). Available from:www.nice.org.uk/CG048

• Implantable cardioverter defibrillators for arrhythmias(review of technology appraisal guidance 11).NICE technology appraisal guidance 95 (2006).Available from: www.nice.org.uk/TA095

• Atrial fibrillation: the management of atrial fibrillation.NICE clinical guideline 36 (2006). Available from:www.nice.org.uk/CG036

• Chronic heart failure: management of chronic heartfailure in adults in primary and secondary care.NICE clinical guideline 5 (2003). Available from:www.nice.org.uk/CG005

National Institute for Health and Clinical ExcellenceMidCity Place, 71 High Holborn, London WC1V 6NA; www.nice.org.uk N1265 1P 15k May 07

Published by the National Institute for Health and Clinical Excellence, May 2007; ISBN 1-84629-420-7

© National Institute for Health and Clinical Excellence, May 2007. All rights reserved. This material may be freelyreproduced for educational and not-for-profit purposes. No reproduction by or for commercial organisations, or forcommercial purposes, is allowed without the express written permission of the Institute.