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(1)

Jen & Amit

With help from City heart failure CNS team

(2)

The last battleground of

heart disease!

∗Congenital / valvular disease - corrected by surgeons

∗Incidence of valvular disease - reduced by

immunisation

∗Endocarditis/ myocarditis - treated and prevented by

use antibiotics

∗HTN and high cholesterol - drug therapy

(3)

NICE 2010

Definition Chronic HF

∗Heart failure is a complex clinical syndrome of symptoms and

signs that suggest impairment of the heart as a pump supporting physiological circulation

∗Caused by structural / functional abnormality heart

∗Initially HF concentrated on pts with reduction systolic function ∗Over last decade more evident almost half of the patients with

HF syndrome do not have LVSD

(4)

Class I - Asymptomatic

Class II –

SOB/ fatigue with normal

activity

Class III - SOB/ fatigue with < ordinary

activity

Class IV – SOB/ fatigue at rest – end stage

(5)
(6)

∗900,000 people in the UK with HF

∗HF LVSD improved survival IHD & effective treatment HF

∗HFPEF ↑ due to increase in survival HTN DM AF ↑

obesity

NICE 2010

Incidence and

(7)

∗6 month mortality rate ↓ from 26 % in 1995 to 14

% 2005

∗Inpatient mortality ↓ 15 % 2005 to 12% 2009

∗Still significant mortality risk 5 year survival 58%

compared to 93% in the age –sex matched general population

∗HF still has a poor prognosis 30 -40 % of pts. die within 1

year

∗ After 1st year mortality is less than 10% per year

NICE 2010

Mortality over last

(8)

∗HF accounts for 2% inpatient bed and 5 % acute

admissions.

∗Over next 25 years predicted to rise by 50 % largely due to

ageing population / improved survival HF / IHD

∗Accounts 2% NHS budget 70 % due to hospitalisation.

∗Length of stay 7-8 days. 25% readmitted within 3 months

(9)

GP numbers

30 patients on list with HF

New diagnosis of 10 per year

2-3 visits to the GP per year

1/3 have severe and prolonged

(10)

Seasonal Variations

Increased deaths over the winter months

more prevalent over 75’s

9000 deaths CVD

Impact seasonal flu with chronic conditions

(11)
(12)
(13)

75% Coronary artery disease –Iscahemia/ MI/ HTN

Valvular & congenital heart disease

Arrhythmias

Diabetes mellitus - consider HF preserved systolic function

Alcohol & Drugs – Cardiac depressants Verapermil, Chemotherapy doxorubicin

Pericardial disease –Constrictive pericarditis pericardial effusions

High output failure – Anaemia Thyrotoxicosis

Pulmonary Disease – Right sided HF Pulmonary hypertension

Heart Failure Preserved ejection fraction - HFPEFcardiomyopathy

(14)

Cardiomyopathy

(15)

∗Normal

∗EF >60% ∗Hypokinesia

∗EF <40%

∗Akinetic

∗Aneurysm ∗∗DysynchronyDyskinesia ∗Aysynchrony

(16)
(17)

I feel old Broken

sleep

Frightened of pain

Tablets causing problems

Depressed Feeling

unwell

Can’t just get my head round

it all

Reliant on other people

Can’t drive

Not really in control

Can’t talk to family/ don’t want to burden

them Breathlessness

Spending too much time at hospitals

Concerns of patients & careers

(18)

Taking a History from Heart Failure

Patient

∗Presenting symptoms

∗Chest Pain - nature character

∗Dyspnoea - exertion/ rest/ sleeping ∗Syncope - collateral history

∗Palpitations - high % HF patients have arrhythmias ∗Cough - associated with co morbidity or medication ∗Oedema - 3kg can be in tissue before see oedema ∗Fatigue - acceptance of slowing down

∗Mood

∗Cardiac and medical history

(19)

∗SoB

∗Persistent cough

∗Nausea

∗Poor appetite

∗Weight gain ∗Bloated

∗Thirsty

∗Swollen limbs

Fatigue

Lack of mobility

Loss Independence Inability to sleep Reduced social activity

Poor memory Low in mood

(20)

Clinical assessment

∗Respiration / Breathing

∗ Have a conversation/

accessory muscles

∗ Crepitations ∗ Effusions ∗ Sats on air

∗Cardiac

∗ BP sitting & standing ∗ Signs overload

∗ HR - check apex

∗ Additional heart sounds

∗ Skin

∗ Temperature and colour limbs ∗ Cap refill

∗ Oedema

∗ Broken areas ∗ Muscle tone

∗ Nutrition

∗ Cachexia - checking LFT Albumin

(21)
(22)
(23)
(24)
(25)
(26)

∗ ACE inhibitors – lead to a fall in angiotensin II and

aldosterone

∗ Reversal of effects of vasoconstriction and sodium

retention

∗ Increases cardiac output

∗ Improved tissue perfusion

∗ Complex effects on tissue structure sensory nerve function,

help prevent poor structural remodelling .

∗ Wealth of evidence that ACE inhibitors improve symptoms,

morbidity and mortality in patients with systolic dysfunction

(27)
(28)

Symptomatic hypotension

headache dizziness fatigue increase risk

falls

ACE inhibitors - dry cough

Renal impairment - Hyperkalaemia

Rash associated pruritus and urticaria

Sinusitis rhinitis sore throat

Angio-oedema particularly Afro-Caribbean

(29)

∗Blockade of the direct toxic effects of catecholamines

∗Reduction of systemic vascular resistance (short term BB increase

SVR)

∗Anti - arrhythmic action (incidence sudden cardiac death NYHA II)

∗Reduction in renin secretion

∗Prolonged diastolic filling permitting increased effective

myocardial blood flow

∗Reduced myocardial ischemia

∗Slowing of the heart rate, reduction myocardial O2 demand

(30)

∗Evidence of systolic dysfunction – accurate diagnosis / aetiology.

∗Patients stable on ACE or AIIB inhibitors at least 2 weeks

No previous history of asthma/ wheeze or syncope

∗Caution:

∗ Concomitant medication that can reduce rate and increase

refraction AV node - Amiodarone, Digoxin, Amlodopine.

∗ PVD

∗ Insulin dependant diabetics history hypoglycaemia

∗Sexually active – may cause problems with impotence

(31)

∗Heart failure with persistent angina

∗HFPEF

∗ very cautious with pulmonary hypertension

∗Contradiction or intolerance to ACE or AIIB

∗Persistent arrhythmias

∗Generalised tachycardia

∗Persistent hypertension

Consideration for beta blockers

when not entirely evidence

(32)

Beta-Blocker in the

(33)

∗Fatigue

∗Low in mood

∗Abdominal upset/ nausea

∗Bradycardia - Brady arrhythmias due to AV block ∗Symptomatic hypotension

∗↓B/P ↓renal perfusion ↑Na+ retention ↑Plasma volume

∗Feeling cold - intermittant claudication ∗Disturbed sleep

∗Exacerbation Psoriasis ∗Wheeze

∗Changes in glucose tolerance ∗Sexual dysfunction loss libido ED

(34)

Seek specialist advice and consider adding one of the following if pt remains symptomatic despite optimal therapy with an ACE

inhibitor & b-blocker:

Aldosterone antagonist esp NYHA class III–IV or MI in past month

ARB licensed esp NYHA class II-III

Hydralazine in combination with nitrate esp in Afro-Carribeans with NYHA class III-IV

(35)

∗RALES study highlighted the possibility that inhibition of the action of

aldosterone may have an impact beyond that expected from further natriuresis and improved electrolyte balance.

∗Addition of Spironolactone to ACE reduced incidence of death by 35% in patients with grade III IV heart failure.

∗Dosage of Spironolactone was small to reduce the incidence of hyperkalaemia

∗ Regular follow up renal function

∗Eplerenone* post MI with clinical heart failure – for pts intolerant to

Spironolactone

(36)

∗22% CRF - Creatinine over 230

∗8 % K > 6.0 mmols  Reduce alternative days rather

than stopping

∗8% Gastric upset chronic diarrhoea/ gynaecomastia ∗4% Poor compliance

∗Labour intensive - little support in community for

vene-puncture

(37)

Symptomatic relief - reduction preload.

No evidence loop and thiazide diuretics offer any prognostic benefit

∗Loop diuretics

∗ Powerful action with rapid onset 5 min IV, 30 min orally lasting up to 4-6

hours.

∗Thiazides

∗ Less effect with reduced eGFR – more common in elderly patients ∗ Close monitoring risk hyponatraemia / hypokalaemia

∗ Useful in pts with persistent HTN ∗ Action 1-2 hours last up to 24 hours.

Diuretic use in systolic dysfunction

(38)

Diuretic therapy

∗Dose depending upon renal

function

∗Difficulty with diuretics ∗ Poor absorption

∗ Over diuresis ∗ Poor mobility ∗ Incontinence

∗Dignity commode in living room

∗Consider fluid/ salt intake ∗Monitor weight

∗Lowest dose possible to achieve

stable weight avoid dehydrated patient

(39)
(40)

Who should get which device

∗Titrate all patients to maximum tolerated evidence based

medical therapy

∗Patients with persistent NYHA III –IV symptoms EF <35%

and QRS >120ms with echo dyssynchrony but SR

considered for CRT

∗Those patients with above and conventional indications for ICD

documented ventricular arrhythmias CRTD

∗Those patients with EF <30% after myocardial infarction and

(41)
(42)

∗Max 2L/ day – where at least moderate overload and

congestion

∗Severely overloaded - 1.5L/day, tighter if hyponatraemia

∗Avoid causing distress – will have a natural thirst

∗Avoid dehydrating drinks ie caffeine, fizzy drinks

∗Advise cold drinks, small ice lollies, flavoured ice cubes, if not

diabetic a boiled sweet, extra soft fruit ie pear

∗Size of the cup - spread drinks

(43)

∗In acute heart failure rest can reduce symptoms and help

relieve oedema

∗ Improves renal blood flow and response to natriuretic response to

diuretics

∗ ↓ sympathetic and renin angiotensin systems

Little evidence that rest is any benefit in stable chronic

heart failure, rather numerous benefits from carefully increasing physical exertion

∗ Skeletal perfusion ∗ Respiratory function

∗Improves autonomic function reversing pathophysiological changes

(44)

∗Adequate and appropriate nutritional balance – consider co-morbidities

∗Poor nutrition may contribute to cardiac cachexia- high risk advanced heart failure - metabolic rate increased up to 20%

∗Poor appetite common

∗ Drug induced – Digoxin, amiodarone, aspirin, statins ∗ Hepatic congestion

∗ Co-morbidities – CRF

∗Specific advise on Salt 6g /Sodium 2g intake per day

(45)

Dietary

If obese weight loss should be encouraged ↑ BMI ↑ cardiac

(46)

∗Encourage all smokers to give up

∗Smoking has adverse haemodynamic effect ↓cardiac output

∗ Increase heart rate and blood pressure ↑ myocardial O2 demand

∗ ↑ carboxyhaemoglobin risk of emboli

∗Restrict alcohol and with related cardiomyopathy abstain completely

∗Alcohol has myocardial depressant properties – in excess predisposes to arrhythmias especially atrial fibrillation

∗Volume may also lead to alterations in fluid balance

(47)
(48)

∗Knowing stable weight

∗ same time day each day then couple of times a week

∗Watch for increased oedema

∗ Awareness what can cause increase fluid volume ↑Sodium / NSAID

∗Self adjusting of diuretics

∗ Pre set guidance to adjust by one dose loop diuretic for set day

∗Knowing when to cut back

∗ D&V/ hot weather

∗ Travelling if poor access to toilet facilities

∗Knowing who to contact

∗ How often need U&Es

∗ Contact numbers for exacerbation symptoms

(49)

Focus CNS HF Role

∗ Post Discharge Visit

∗ Education chronic disease life style and ADL’s

∗ Monitoring Complex Patients

∗ Titration Medication

∗ Concordance issues

∗ Review stable patients step down from service

∗ On going support poorly patients

∗ Palliative and terminal care .

(50)

HF CNS SOS review

∗In 1 month 16 SOS calls to HFN

∗9 would have called GP

∗7 would have called ambulance

∗All were discussed at monthly HF CNS team meeting

(51)

Initial diagnosis

Management of severe heart failure (NYHA class IV),

Not responding to treatment

Can no longer be managed at home

Planning a pregnancy or are pregnant

Heart failure due to valve disease

Consideration of devices

NICE 2010

(52)

Long term monitoring

patient

∗Despite widespread use of ACE

inhibitors and beta-blockers, both

shown to prolong survival and reduce mortality, optimal management

remains poor.

∗Randomised studies examining the

(53)

∗Different agendas - keeping consultations on track and remaining holistic

∗Adherence to medication – 0ver lifespan

∗Inconsistent advice – HF usually secondary already received advice

∗Recognising own limitations - working with MDT

∗Lack of resources, access to investigations

∗Lack respite facilities – limited resources palliative care

(54)
(55)

Cancer Heart failure

(56)

Phase 1 Symptom onset,

diagnosis and initiation of

medical treatment. Often started by hospital admission 

medication and education

Phase 2 Under the care of

community teams. Ongoing support and education for

patents and carers  promote autonomy, self care, adherence, when to call for help and reduce inappropriate admissions.

(57)

Phase 3 Periods of instability with

recurrence of symptoms due to deterioration in heart function 

Rebalancing of treatment, implantable cardiac devices.

Phase 4 Increasing symptoms &

declining physical capacity, despite optimal therapy.

Phase 5 Multi-organ failure 

Supportive and palliative care needs.

(58)

Trajectory of death

indications

Signs organ failure

∗ Worsening renal function

∗ Dropping Sodium and potassium ∗ Liver function congested pattern

Falling Haemoglobin – associated with CRF ∗ Gallop rhythm

∗ Persistent tachycardia -

∗ Increased activation and firing ICD if implanted

Unexplained weight loss

Worsening of co-morbidities

(59)
(60)

Supportive Care

∗ Identify & Treat Aetiology ∗ Additional investigations ∗ Active Treatment

∗ Devices

∗ Motivation - self belief ∗ Self manage, target risk

factors

∗ Encourage coping ∗ Enhance Hope

Palliative Care

∗QoL

∗Symptom management ∗Minimise medication ∗Anticipatory meds ∗Preparing for end of

natural life

∗Consider inactivate ICD ∗Consider place of death ∗Reduce fears, comfort

(61)

Palliative Care and Heart Failure

∗ Decision to discontinue active treatment and adopt palliative

approach is rarely encountered

∗ Lack of acknowledgement to change the emphasis of treatment to

symptom management

∗ Identification of the point of transition to a terminal phase is very

difficult, may have survived previous life threatening episode

∗ High prevalence of unexpected death, impact on carer and

(62)

∗Heart failure is a common disease and its on the increase

∗There are growing number of evidence based therapies

that can improve both prognosis and reduce morbidity.

∗Life style skills offered to patients can improve stability

∗The diagnosis is often missed and the patients are often

under treated

∗Provision for palliative care is under funded considering

the mortality and malignant nature of the disease

∗Lack dedicated workforce - aim to raise awareness to

wider MDT

References

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