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Dive into the research topics where C. O'Loughlin is active.

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Featured researches published by C. O'Loughlin.


European Journal of Heart Failure | 2005

Clinical deterioration in established heart failure: What is the value of BNP and weight gain in aiding diagnosis?

Jennifer Lewin; Mark Ledwidge; C. O'Loughlin; Clare McNally; Kenneth McDonald

Weight gain and increase in B‐Type Natriuretic Peptide have been advocated as means of aiding diagnosis of heart failure. However, there are few data to support the use of these criteria in diagnosing clinical deterioration in patients with established disease.


European Journal of Heart Failure | 2009

A comparative study of the palliative care needs of heart failure and cancer patients

Norma O'Leary; Niamh F. Murphy; C. O'Loughlin; Eoin Tiernan; Kenneth McDonald

Studies suggest that patients with advanced heart failure (HF) have unmet palliative care (PC) needs. However, many of these studies have been retrospective or based on patients receiving poorly coordinated ad hoc care. We aimed to demonstrate whether the PC needs of patients with advanced HF receiving specialist multidisciplinary coordinated care are similar to cancer patients deemed to have specialist PC needs; thereby justifying the extension of specialist PC services to HF patients.


European Journal of Heart Failure | 2009

Diagnosis of heart failure with preserved ejection fraction: improved accuracy with the use of markers of collagen turnover

Ramon Martos; John Baugh; Mark Ledwidge; C. O'Loughlin; Niamh F. Murphy; Carmel Conlon; Anil Patle; Seamas C. Donnelly; Kenneth McDonald

Heart failure with preserved ejection fraction (HF‐PEF) can be difficult to diagnose in clinical practice. Myocardial fibrosis is a major determinant of diastolic dysfunction (DD), potentially contributing to the progression of HF‐PEF. The aim of this study was to analyse whether serological markers of collagen turnover may predict HF‐PEF and DD.


International Journal of Cardiology | 2010

Quality of life predicts outcome in a heart failure disease management program

C. O'Loughlin; Niamh F. Murphy; Carmel Conlon; Aoife O'Donovan; Mark Ledwidge; Kenneth McDonald

BACKGROUND Chronic heart failure (HF) is associated with a poor Health Related Quality of Life (HRQoL). HRQoL has been shown to be a predictor of HF outcomes however, variability in the study designs make it difficult to apply these findings to a clinical setting. The aim of this study was to establish if HRQoL is a predictor of long-term mortality and morbidity in HF patients followed-up in a disease management program (DMP) and if a HRQoL instrument could be applied to aid in identifying high-risk patients within a clinical context. METHODS This is a retrospective analysis of HF patients attending a DMP with 18+/-9 months follow-up. Clinical and biochemical parameters were recorded on discharge from index HF admission and HRQoL measures were recorded at 2 weeks post index admission. RESULTS 225 patients were enrolled into the study (mean age=69+/-12 years, male=61%, and 78%=systolic HF). In multivariable analysis, all dimensions of HRQoL (measured by the Minnesota Living with HF Questionnaire) were independent predictors of both mortality and readmissions particularly in patients <80 years. A significant interaction between HRQoL and age (Total((HRQoL))age: p<0.001) indicated that the association of HRQoL with outcomes diminished as age increased. CONCLUSIONS These data demonstrate that HRQoL is a predictor of outcome in HF patients managed in a DMP. Younger patients (<65 years) with a Total HRQoL score of > or =50 are at high risk of an adverse outcome. In older patients > or =80 years HRQoL is not useful in predicting outcome.


European Journal of Heart Failure | 2008

Outpatient intravenous diuretic therapy; potential for marked reduction in hospitalisations for acute decompensated heart failure

Mary Ryder; Niamh F. Murphy; Dermot McCaffrey; C. O'Loughlin; Mark Ledwidge; Kenneth McDonald

Heart failure patients have frequent readmissions for acute decompensated heart failure (ADHF).


European Journal of Heart Failure | 2005

Heart failure care in a hospital unit: a comparison of standard 3-month and extended 6-month programs.

Mark Ledwidge; Enda Ryan; C. O'Loughlin; Mary Ryder; Bronagh Travers; Emma Kieran; Allison Walsh; Kenneth McDonald

We have previously shown that a structured in‐hospital and outpatient heart failure (HF) program reduces clinical events over a 3‐month period following hospital discharge.


American Journal of Cardiology | 2009

Causes and consequences of nonpersistence with heart failure medication.

Mary Mockler; C. O'Loughlin; Niamh F. Murphy; Mary Ryder; Carmel Conlon; Kenneth McDonald; Mark Ledwidge

Persistence with therapy may be more easily and objectively identified in the clinical setting than compliance and recent work has shown it to be linked to mortality in heart failure (HF). The aim of this study was to determine the extent, causes, and clinical impact of nonpersistence with disease-modifying therapy in a retrospective cohort study of 183 patients with systolic HF participating in a disease management program. The main outcome measurements were reasons/determinants of nonpersistence and its impact on hospitalizations. Fifty-three patients (29%) had 74 separate occurrences of nonpersistence with disease-modifying therapy. There was no medical reason for discontinuing medications in 50% of occurrences, whereas medication was discontinued for an adverse reaction in 30% and for a justified medical reason in 15% of occurrences. Nonpersistence was a significant predictor of all-cause readmission (hazard ratio 3.20, 95% confidence interval 1.74 to 11.37) and cardiovascular readmission (hazard ratio 4.45, 95% confidence interval 1.74 to 11.37). In the adjusted model, there was no significantly increased risk of HF readmission (hazard ratio 2.41, 95% confidence interval 0.88 to 6.62). In conclusion, nonpersistence with HF therapy is common, is often not medically justified, and is associated with an increased risk of hospitalization.


Journal of Cardiac Failure | 2008

Multiple Neurohumoral Modulating Agents in Systolic Dysfunction Heart Failure: Are We Lowering Blood Pressure Too Much?

G. Mak; Niamh F. Murphy; Akbar Ali; Alison Walsh; C. O'Loughlin; Carmel Conlon; Dermot McCaffrey; Mark Ledwidge; Kenneth McDonald

BACKGROUND Disease-modifying drug treatment in heart failure (HF) reduces blood pressure. Titration of these agents is guided by clinic blood pressure readings; however, the impact of such treatment on blood pressure is unknown because diurnal blood pressure patterns remain poorly described. The aim of this study was to examine the impact of additional neurohumoral modulating agents on ambulatory blood pressure monitoring (ABPM) control in patients with systolic HF and examine the relationship between the burden of hypotension and clinical outcomes. METHODS AND RESULTS In a prospective analysis on 45 patients undergoing initiation and optimization of additional medications (angiotensin-converting enzyme inhibitors, angiotensin II receptor blockers, or beta-blockers), mean daytime systolic (P = .035) and mean daytime and nocturnal diastolic hypotensive episodes (both P < .001) increased significantly posttitration. There was no change in clinic blood pressure before and after titration. In a cross-sectional analysis on 144 patients, those with the most diastolic hypotensive episodes had higher rates of HF readmissions (P = .01) and the composite end point of all-cause mortality and all-cause readmissions (P = .03). CONCLUSIONS Additional neurohumoral modulating agents could produce significant increases in 24-hour hypotension burden despite reassuring clinic blood pressure readings. The burden of diastolic hypotension is independently predictive of HF readmissions and the composite end point of all-cause mortality and emergency readmissions.


European Journal of Heart Failure | 2007

Improvement but no cure of left ventricular systolic dysfunction in treated heart failure patients.

Niamh F. Murphy; C. O'Loughlin; Mark Ledwidge; Dermot McCaffrey; Kenneth McDonald

Recent advances in pharmacological and pacemaker‐based treatments for heart failure (HF) have brought about significant improvements in left ventricular function.


Clinical Chemistry and Laboratory Medicine | 2011

B-type natriuretic peptide measurement in primary care; magnitude of associations with cardiovascular risk factors and their therapies. Observations from the STOP-HF (St. Vincent's Screening TO Prevent Heart Failure) study.

Carmel Conlon; Ian Dawkins; C. O'Loughlin; Denise Gibson; Cecily Kelleher; Mark Ledwidge; Kenneth McDonald

Abstract Background: An effective prevention strategy for heart failure in primary care requires a reliable screening tool for asymptomatic ventricular dysfunction. Preliminary data indicate that B-type natriuretic peptide (BNP) may be suitable for this task. However, for the most effective use of this peptide, the interrelationships between associated risk factors and their therapies on BNP, and in particular their magnitude of effect, needs to be established in a large primary care population. Therefore, the objective of the study was to establish the extent of the association between BNP, cardiovascular risk factors and their therapies. Methods: BNP measurement and clinical review was preformed on 1122 primary care patients with cardiovascular risk factors. Multivariate analyses identified significant associates of BNP concentrations which were further explored to establish the magnitude of their association. Results: Associates of BNP were age (1.36-fold increase in BNP/decade), female (1.28), β-blockers (1.90), myocardial infarction (1.36), arrhythmia (1.98), diastolic blood pressure; all p<0.01. A novel method was devised that plotted median BNP per sliding decade of age for the various combinations of these principal associates. Conclusions: The data presented underline the importance of considering several clinical and therapeutic factors when interpreting BNP concentrations. Most of these variables were associated with increased concentrations, which may in part explain the observed false-positive rates for detecting ventricular dysfunction using this peptide. Furthermore, the design of studies or protocols using BNP as an endpoint or a clinical tool should take particular account of these associations. This analysis provides the foundation for age, risk factor and therapy adjusted reference ranges for BNP in this setting.

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Mark Ledwidge

University College Dublin

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C. Conlon

University College Cork

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Carmel Conlon

University College Dublin

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Cecily Kelleher

University College Dublin

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G. Mak

University College Dublin

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Mary Ryder

University College Dublin

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John Baugh

University College Dublin

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