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1.
ESC Heart Fail ; 9(1): 186-195, 2022 02.
Article in English | MEDLINE | ID: mdl-34877822

ABSTRACT

AIMS: This study aimed to describe haemodynamic features of patients with advanced heart failure with preserved ejection fraction (HFpEF) as defined by the Heart Failure Association (HFA) of the European Society of Cardiology (ESC). METHODS AND RESULTS: We used pooled data from two dedicated HFpEF studies with invasive exercise haemodynamic protocols, the REDUCE LAP-HF (Reduce Elevated Left Atrial Pressure in Patients with Heart Failure) trial and the REDUCE LAP-HF I trial, and categorized patients according to advanced heart failure (AdHF) criteria. The well-characterized HFpEF patients were considered advanced if they had persistent New York Heart Association classification of III-IV and heart failure (HF) hospitalization < 12 months and a 6 min walk test distance < 300 m. Twenty-four (22%) out of 108 patients met the AdHF criteria. On evaluation, clinical characteristics and resting haemodynamics were not different in the two groups. Patients with AdHF had lower work capacity compared with non-advanced patients (35 ± 16 vs. 45 ± 18 W, P = 0.021). Workload-corrected pulmonary capillary wedge pressure normalized to body weight (PCWL) was higher in AdHF patients compared with non-advanced (112 ± 55 vs. 86 ± 49 mmHg/W/kg, P = 0.04). Further, AdHF patients had a smaller increase in cardiac index during exercise (1.1 ± 0.7 vs. 1.6 ± 0.9 L/min/m2 , P = 0.028). CONCLUSIONS: A significantly higher PCWL and lower cardiac index reserve during exercise were observed in AdHF patients compared with non-advanced. These differences were not apparent at rest. Therapies targeting the haemodynamic compromise associated with advanced HFpEF are needed.


Subject(s)
Heart Failure , Atrial Pressure , Heart Failure/therapy , Hemodynamics , Humans , Stroke Volume , Ventricular Function, Left
3.
Int J Clin Pract ; 62(10): 1515-9, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18036168

ABSTRACT

BACKGROUND: Pericardial effusions frequently present challenging clinical dilemmas. Whether or not to drain an effusion, and if so by what method, are two common decisions facing cardiologists. We performed a survey to evaluate pericardiocentesis practice in the United Kingdom (UK). METHODS: A total of 640 questionnaires were sent to all cardiologists in the UK Directory of Cardiology in March 2003. RESULTS: A total of 274 (43%) completed questionnaires were returned, 88% from consultants, equally distributed between tertiary referral centres and district general hospitals. More than 1500 procedures were performed, largely using a paraxiphoid approach (89%). Clinical tamponade was the commonest indication for pericardiocentesis (83%). However, the majority of respondents (69%) considered echocardiographic features alone an indication for pericardiocentesis, even in the absence of clinical tamponade. The commonest perceived indications for drainage were right ventricular diastolic collapse and right atrial collapse (69% and 33% of respondents respectively). For guidance, 82% use echocardiography, either alone or with fluoroscopy or the electrocardiogram (ECG) injury trace. 11% employ fluoroscopy alone or with the ECG injury trace. The remaining 11% stated that they would use the ECG injury trace alone or use no guidance. Using the ECG injury trace alone is said by the European Society of Cardiology (ESC) guidelines to offer an inadequate safeguard. Reported complications included ventricular puncture (n = 12, 0.8%) and hepatic damage (n = 4, 0.3%). CONCLUSION: Pericardiocentesis practice varies substantially in the UK. Many cardiologists would perform pericardiocentesis based on echocardiographic features alone. 11% of cardiologists use guidance that is considered inadequate by the ESC guidelines.


Subject(s)
Cardiology/methods , Pericardiocentesis/methods , Professional Practice/standards , Consultants , Humans , Pericardial Effusion/etiology , Pericardial Effusion/therapy , Pericardiocentesis/adverse effects , Pericardiocentesis/standards , Surveys and Questionnaires , United Kingdom
4.
Obes Rev ; 19(9): 1189-1204, 2018 09.
Article in English | MEDLINE | ID: mdl-30051959

ABSTRACT

OBJECTIVE: Obesity is an independent risk factor for the development of heart failure, and the two commonly co-exist. The European Society of Cardiology does not provide guidance regarding weight loss strategies in heart failure. The aim of this study was to systematically review the evidence for outcomes following intentional weight loss in patients with heart failure and obesity. METHOD: A systematic review of English articles was undertaken using databases PubMed, Embase and CENTRAL. Randomized controlled trials and observational studies reporting outcomes following intentional weight loss by lifestyle, surgical or pharmacotherapy intervention in patients with obesity and heart failure were included. RESULTS: Four randomized controlled trials and seven observational studies were identified. Two randomized controlled trials used diet and exercise as an intervention, one used diet alone and one used a pharmacological intervention (orlistat). All but one reported significant weight loss. Two reported improvement in exercise capacity and quality of life. One reported improvement in New York Heart Association functional class in heart failure with preserved ejection fraction. The observational studies, five of which reported on outcomes following bariatric surgery, despite being small, heterogeneous and high risk of bias, suggested a trend in improvement of left ventricular function, quality of life and exercise capacity following weight loss. CONCLUSION: Weight loss is achievable with lifestyle intervention in those with heart failure and obesity and may result in improvements in New York Heart Association classification, quality of life and exercise capacity.


Subject(s)
Heart Failure/physiopathology , Obesity/therapy , Weight Loss/physiology , Anti-Obesity Agents/therapeutic use , Body Mass Index , Diet, Reducing , Exercise/physiology , Heart Failure/complications , Humans , Obesity/complications , Obesity/physiopathology , Orlistat/therapeutic use , Quality of Life
5.
Circulation ; 103(10): 1378-81, 2001 Mar 13.
Article in English | MEDLINE | ID: mdl-11245639

ABSTRACT

BACKGROUND: -Urotensin II (UII) is the ligand for the GPR14 receptor and the most potent vasoconstrictor in the cynomolgus monkey. UII also contracts rat thoracic aorta. We studied the effect of human UII (hUII) in human blood vessels Methods and Results-Small subcutaneous resistance arteries, internal mammary arteries, saphenous veins, and small subcutaneous veins were studied using standard techniques. Subcutaneous resistance arteries constricted in response to norepinephrine (maximum tension, 2.84+/-0.38 mN/mm; the concentration required to produce 50% of the maximum response [EC(50)], 0.52+/-0.07 micromol/L) and endothelin-1 (maximum tension, 4.19+/-0.93 mN/mm; EC(50), 1.6+/-0.1 nmol/L). hUII did not contract these arteries, internal mammary arteries, or either type of vein, but it was a potent vasoconstrictor in rat thoracic aorta (maximum tension, 2.36+/-0.2 mN/mm; EC(50), 1.13+/-0.36 nmol/L). CONCLUSIONS: -hUII has no vasoconstrictor action in human arteries and veins of different sizes and vascular beds. Marked species differences in the actions of UII question its importance in human cardiovascular regulation.


Subject(s)
Arteries/drug effects , Urotensins/pharmacology , Vasoconstriction/drug effects , Vasoconstrictor Agents/pharmacology , Veins/drug effects , Adult , Aged , Animals , Aorta, Thoracic/drug effects , Aorta, Thoracic/physiology , Arteries/physiology , Humans , Male , Middle Aged , Rats , Species Specificity , Veins/physiology
6.
Circulation ; 104(15): 1805-8, 2001 Oct 09.
Article in English | MEDLINE | ID: mdl-11591618

ABSTRACT

BACKGROUND: [Pro(11)(D)-Ala(12)] angiotensin I is an ACE-resistant substrate specific for chymase. We used this peptide to determine whether a functionally significant non-ACE angiotensin (Ang) II-generating pathway exists in human dorsal hand veins. METHODS AND RESULTS: Using a modified Aellig technique, we studied the response to Ang I and [Pro(11)(D)-Ala(12)] Ang I in dorsal hand veins in vivo in patients with coronary heart disease. We measured the venoconstrictor effect of each peptide given before and after a 6.25-mg oral dose of the ACE inhibitor captopril or matching placebo. Placebo or captopril was given in a double-blind, randomized fashion. Ang I induced a mean+/-SEM venoconstrictor response of 45+/-11%, 40+/-10%, 55+/-8%, and 4+/-4% before placebo, after placebo, before captopril, and after captopril, respectively. Hence, the response to Ang I was reproducible and was reduced significantly only after treatment with captopril (P=0.002). [Pro(11)(D)-Ala(12)] Ang I induced a mean venoconstrictor response of 42+/-9%, 49+/-9%, 48+/-10%, and 54+/-11% before placebo, after placebo, before captopril, and after captopril, respectively. Hence, captopril had no significant effect on the response to [Pro(11)(D)-Ala(12)] Ang I. CONCLUSIONS: We have demonstrated that [Pro(11)(D)-Ala(12)] Ang I is able to induce venoconstriction in humans in vivo. With this specific pharmacological probe, we have shown that a non-ACE pathway capable of generating Ang II exists in human veins in vivo and is potentially functionally important. This pathway is likely to involve the enzyme chymase.


Subject(s)
Angina Pectoris/physiopathology , Angiotensin I/analogs & derivatives , Angiotensin I/pharmacology , Vasoconstriction/drug effects , Veins/drug effects , Veins/physiopathology , Administration, Oral , Angina Pectoris/drug therapy , Angiotensin I/metabolism , Angiotensin II/biosynthesis , Angiotensin Receptor Antagonists , Angiotensin-Converting Enzyme Inhibitors/administration & dosage , Antihypertensive Agents/administration & dosage , Biphenyl Compounds/administration & dosage , Captopril/administration & dosage , Chronic Disease , Chymases , Dose-Response Relationship, Drug , Double-Blind Method , Hand/blood supply , Humans , Infusions, Intravenous , Irbesartan , Middle Aged , Peptidyl-Dipeptidase A/metabolism , Reproducibility of Results , Serine Endopeptidases/metabolism , Substrate Specificity , Tetrazoles/administration & dosage
7.
J Am Coll Cardiol ; 37(4): 1056-61, 2001 Mar 15.
Article in English | MEDLINE | ID: mdl-11263608

ABSTRACT

OBJECTIVES: We sought to demonstrate non-angiotensin converting enzyme (ACE) dependent angiotensin II (AII) generating pathways in resistance arteries from patients with chronic heart failure (CHF). BACKGROUND: Non-ACE dependent AII generation occurs in resistance arteries from normal volunteers. Inhibition of non-ACE dependent AII generation may have therapeutic potential in CHF. METHODS: Resistance arteries were dissected from gluteal biopsies from patients with coronary heart disease (CHD) and preserved left ventricular function and from patients with CHF. Using wire myography, concentration response curves to angiotensin I (AI) and AII were constructed in the presence of 1) vehicle, 2) chymostatin [an inhibitor of chymase], 3) enalaprilat, and 4) the combination of chymostatin and enalaprilat. RESULTS: In resistance arteries from patients with CHD, the vasoconstrictor response to AI was not inhibited by either inhibitor alone (chymostatin [p > or = 0.05] or enalaprilat [p > or = 0.05]) but was significantly inhibited by the combination (p < 0.001). In arteries from patients with CHF, AI responses were inhibited by enalaprilat (p < 0.05) but not by chymostatin alone (p > 0.05). The combination ofchymostatin and enalaprilat markedly inhibited the response to AI (p < 0.001) to a greater degree than enalaprilat alone (p < or = 0.01). CONCLUSIONS: Non-ACE dependent AII generating pathways exist in resistance arteries from patients with both CHF and CHD. In resistance arteries from patients with CHD, inhibition of either the ACE or chymase pathway alone has no effect on AII generation, and both pathways must be blocked before the vasoconstrictor action of AI is inhibited. In CHF, blockade of ACE results in marked inhibition of responses to AI, but this is enhanced by coinhibition of chymase. These studies suggest that full suppression of the renin-angiotensin system cannot be achieved by ACE inhibition alone and provide a rationale for developing future therapeutic strategies.


Subject(s)
Angina Pectoris/physiopathology , Angiotensin II/metabolism , Angiotensin-Converting Enzyme Inhibitors/pharmacology , Arteries/metabolism , Heart Failure/metabolism , Peptidyl-Dipeptidase A/metabolism , Acetylcholine/pharmacology , Aged , Angiotensin I/metabolism , Angiotensin I/pharmacology , Angiotensin II/antagonists & inhibitors , Angiotensin II/pharmacology , Arteries/drug effects , Arteries/physiopathology , Bradykinin/pharmacology , Chymases , Enalaprilat/pharmacology , Female , Heart Failure/drug therapy , Heart Failure/physiopathology , Humans , In Vitro Techniques , Losartan/pharmacology , Male , Middle Aged , Oligopeptides/pharmacology , Serine Endopeptidases/metabolism , Vascular Resistance , Vasoconstriction/drug effects
8.
J Hypertens ; 18(1): 61-4, 2000 Jan.
Article in English | MEDLINE | ID: mdl-10678544

ABSTRACT

OBJECTIVE: Adrenomedullin inhibits angiotensin II stimulated aldosterone production in vitro and in vivo in experimental animals. The aim of this study was to investigate the effect of adrenomedullin on angiotensin II and adrenocorticotrophic hormone-stimulated aldosterone production in vivo in healthy humans. DESIGN AND METHODS: Seven volunteers were studied in a quiet, temperature-controlled laboratory. After 35 min of rest, an infusion of placebo or adrenomedullin (3 pmol/kg per min) was given over 60 min; 15 min after starting this first infusion, a second infusion of angiotensin II (0.96 fmol/kg per min) or adrenocorticotrophic hormone (0.1 mIU/kg per min) was co-infused and continued for 45 min. RESULTS: Adrenomedullin significantly inhibited angiotensin II stimulated aldosterone production: the increment in aldosterone on the placebo day was 691 pmol/l compared with 552 pmol/l on the adrenomedullin day (P< 0.004). Adrenomedullin did not inhibit adrenocorticotrophic hormone-stimulated aldosterone or cortisol release. CONCLUSION: Adrenomedullin selectively inhibits angiotensin II-stimulated aldosterone production.


Subject(s)
Aldosterone/metabolism , Angiotensin II/pharmacology , Mineralocorticoid Receptor Antagonists/pharmacology , Peptides/pharmacology , Adrenocorticotropic Hormone/pharmacology , Adrenomedullin , Adult , Blood Pressure/drug effects , Female , Humans , Hydrocortisone/metabolism , Male , Peptides/blood
9.
Eur J Heart Fail ; 3(2): 183-7, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11246055

ABSTRACT

BACKGROUND: Breathlessness is a common symptom experienced by patients with chronic heart failure (CHF) but its etiology remains controversial. Various molecular and histological adaptations have been reported for the diaphragm in CHF but their functional consequences are poorly described. AIMS: This study aims to determine the position and function of the diaphragm in CHF patients. METHODS: The diaphragm position was measured, relative to the renal pelvis, by ultrasound in 20 CHF patients and ninety controls matched for age and body mass. The extent and velocity of diaphragm movement was also measured during quiet breathing and sniffing. RESULTS: At the end of expiration, the diaphragm was significantly nearer to the renal pelvis in CHF patients (89.3+/-16.8 vs. 96.3+/-19.2 mm, P<0.05) and also moved further during quiet breathing (18.2+/-4.4 vs. 12.7+/-4.6 mm, P<0.001) and sniffing (23.9+/-7.4 vs. 18.2+/-5.7 mm, P<0.005). Velocity of diaphragm movement was also increased in CHF patients during quiet breathing (26.5+/-8.2 vs. 15.9+/-6.1 mm s(-1), P<0.001). CONCLUSIONS: These data demonstrate that the position and function of the diaphragm is altered in CHF.


Subject(s)
Diaphragm/diagnostic imaging , Dyspnea/diagnostic imaging , Echocardiography , Heart Failure/diagnostic imaging , Aged , Chronic Disease , Diaphragm/physiopathology , Dyspnea/physiopathology , Female , Heart Failure/physiopathology , Humans , Male , Middle Aged , Ventricular Dysfunction, Left/diagnostic imaging , Ventricular Dysfunction, Left/physiopathology
10.
Eur J Heart Fail ; 1(1): 25-9, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10937975

ABSTRACT

The clinical success of neurohumoral manipulation by ACE inhibitors and beta blockers in heart failure has led to new therapeutic approaches. New neurohumoral factors are now viewed as offering the potential for treatment interventions. Not only do we consider blocking the production of deleterious hormones, but also, more recently, consideration has been given to augmenting the actions of factors with potentially beneficial actions. Hopefully such manipulation of ADM and ET-1 can result in further improvement in the well-being of heart failure patients.


Subject(s)
Endothelin-1/physiology , Heart Failure/physiopathology , Peptides/physiology , Adrenomedullin , Atrial Natriuretic Factor/physiology , Humans , Natriuretic Peptide, Brain/physiology , Vasoconstriction/physiology
11.
BMJ ; 321(7255): 215-8, 2000 Jul 22.
Article in English | MEDLINE | ID: mdl-10903655

ABSTRACT

OBJECTIVES: To characterise the clinical features of patients with suspected heart failure but preserved left ventricular systolic function to determine if they have other potential causes for their symptoms rather than being diagnosed with "diastolic heart failure." DESIGN: Prospective descriptive study. SETTING: Outpatient based direct access echocardiography service. PARTICIPANTS: 159 consecutive patients with suspected heart failure referred by general practitioners. MAIN OUTCOME MEASURES: Symptoms (including shortness of breath, ankle oedema, and paroxysmal nocturnal dyspnoea) and history of coronary heart disease and chronic pulmonary disease. Transthoracic echocardiography, body mass index, pulmonary function tests, and electrocardiography. RESULTS: 109 of 159 participants had suspected heart failure in the absence of left ventricular systolic dysfunction, valvular heart disease, or atrial fibrillation. Of these 109, 40 were either obese or very obese, 54 had a reduction in forced expiratory volume in 1 second to

Subject(s)
Cardiac Output, Low/diagnosis , Cardiac Output, Low/physiopathology , Ventricular Function, Left/physiology , Angina Pectoris/physiopathology , Body Mass Index , Diagnosis, Differential , Diagnostic Errors , Dyspnea/etiology , Dyspnea/physiopathology , Edema/etiology , Electrocardiography/methods , Female , Forced Expiratory Volume/physiology , Humans , Male , Middle Aged , Myocardial Infarction/physiopathology , Obesity/physiopathology , Prospective Studies , Respiration Disorders/diagnosis , Respiration Disorders/physiopathology
12.
BMJ ; 323(7315): 715-8, 2001 Sep 29.
Article in English | MEDLINE | ID: mdl-11576977

ABSTRACT

OBJECTIVES: To determine whether specialist nurse intervention improves outcome in patients with chronic heart failure. DESIGN: Randomised controlled trial. SETTING: Acute medical admissions unit in a teaching hospital. PARTICIPANTS: 165 patients admitted with heart failure due to left ventricular systolic dysfunction. The intervention started before discharge and continued thereafter with home visits for up to 1 year. MAIN OUTCOME MEASURES: Time to first event analysis of death from all causes or readmission to hospital with worsening heart failure. RESULTS: 31 patients (37%) in the intervention group died or were readmitted with heart failure compared with 45 (53%) in the usual care group (hazard ratio=0.61, 95% confidence interval 0.33 to 0.96). Compared with usual care, patients in the intervention group had fewer readmissions for any reason (86 v 114, P=0.018), fewer admissions for heart failure (19 v 45, P<0.001) and spent fewer days in hospital for heart failure (mean 3.43 v 7.46 days, P=0.0051). CONCLUSIONS: Specially trained nurses can improve the outcome of patients admitted to hospital with heart failure.


Subject(s)
Heart Failure/nursing , Nurse Clinicians , Aged , Chronic Disease , Disease-Free Survival , Female , Heart Failure/mortality , House Calls , Humans , Male , Proportional Hazards Models , Treatment Outcome
15.
Neth Heart J ; 11(11): 437-439, 2003 Nov.
Article in English | MEDLINE | ID: mdl-25696156
16.
QJM ; 101(5): 345-9, 2008 May.
Article in English | MEDLINE | ID: mdl-18281365

ABSTRACT

BACKGROUND: Echocardiography is one of the cornerstones of cardiovascular investigation. The escalating demands on echocardiography services necessitate close examination of how we organize our departments on a day-to-day basis, in order to provide a consistent, high-quality service. AIM: To evaluate current transthoracic echocardiography practice in the UK. DESIGN: National postal survey. METHODS: A questionnaire was sent to the chief cardiac physiologist (CP) of every hospital in the UK with echocardiographic facilities. RESULTS: Three hundred and thirty six echocardiographic departments were identified. One hundred and twenty six (37.5%) completed questionnaires were returned. In 87% of hospitals, CPs both performed and reported over 80% of echocardiograms. Fifty-seven percent of CPs and 22% of doctors performing echocardiography held an accreditation in echocardiography. Only 60% of hospitals had formal criteria that had to be met prior to an operator being allowed to report echocardiograms unsupervised. Fewer than half of hospitals regularly audited their echocardiography service. Both outpatient and inpatient waiting times for echocardiography were highly variable and frequently excessive. Fewer than half of hospitals used modern techniques for assessing diastolic function, mechanical dyssynchrony or severity of mitral regurgitation. CONCLUSION: In the UK, many transthoracic echocardiograms are performed and reported by operators without formally assessed competence. Fewer than half of hospitals regularly audited their service or used modern echocardiographic techniques. Services are likely to be improved by developing and instituting mandatory national guidelines.


Subject(s)
Cardiology/standards , Clinical Competence/standards , Echocardiography/statistics & numerical data , Delivery of Health Care/standards , Delivery of Health Care/statistics & numerical data , Echocardiography/standards , Heart Diseases/diagnosis , Hospitals , Humans , Professional Practice/standards , Surveys and Questionnaires , United Kingdom
19.
Heart ; 90(5): 511-7, 2004 May.
Article in English | MEDLINE | ID: mdl-15084546

ABSTRACT

OBJECTIVE: To determine the concordance of different Doppler echocardiographic criteria for "diastolic dysfunction" in patients with suspected heart failure but preserved left ventricular systolic function. DESIGN: Prospective, descriptive study. SETTING: Outpatient based direct access echocardiography service. PATIENTS: Consecutive patients referred with suspected heart failure but preserved left ventricular systolic function. MEASUREMENTS: Echocardiographic measurements of systolic and diastolic function. Eight published studies giving age and sex specific ranges for measures of diastolic function in healthy subjects were reviewed and the proportion of patients outside the normal limits for each of these published ranges was calculated. RESULTS: There was very poor concordance between measures with up to a 16-fold difference in the prevalence of diastolic dysfunction in the overall patient cohort. Even for a given measure, there was relatively poor agreement between the published reference ranges. In subsets likely to include patients at high risk of having diastolic dysfunction, an increased prevalence of diastolic dysfunction was not evident with any measure in any patient subset. CONCLUSIONS: Our findings challenge the use of the diagnosis of diastolic heart failure based on the most commonly used echocardiographic criteria. Physicians should be cautious about echocardiographic reports describing diastolic dysfunction and only apply the diagnosis of diastolic heart failure with great care.


Subject(s)
Cardiac Output, Low/diagnostic imaging , Ventricular Dysfunction, Left/diagnostic imaging , Aged , Cardiac Output, Low/physiopathology , Diastole/physiology , Echocardiography , Echocardiography, Doppler , Female , Humans , Male , Prospective Studies , Reference Values , Risk Factors , Systole/physiology , Ventricular Dysfunction, Left/physiopathology
20.
Eur Heart J ; 19 Suppl P: P9-16, 1998 Dec.
Article in English | MEDLINE | ID: mdl-9886707

ABSTRACT

Clinically overt heart failure is common, costly, disabling, and deadly; it remains so despite the tremendous benefit of angiotensin-converting enzyme inhibitors. Better treatments for and earlier detection of heart failure are needed if the situation to improve. However, even this may not be enough. The dramatic deterioration in quality of life and prognosis when a patient progresses from asymptomatic left ventricular dysfunction to overt heart failure suggests that only a programme of screening and prevention will effectively reduce the public health burden of heart failure. Moreover, the economic consequences of developing overt heart failure suggest that such an approach is likely to be cost-effective.


Subject(s)
Heart Failure/epidemiology , Echocardiography , Epidemiologic Methods , Forecasting , Humans , Prevalence , Quality of Life , Ventricular Dysfunction, Left/epidemiology
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