ABSTRACT
INTRODUCTION: Heart rate (HR) is often elevated in cats with cardiomyopathies (CMPs). Pharmacologic modulation of HR may reduce cardiac morbidity and mortality. OBJECTIVES: To investigate the effects of cilobradine vs. placebo, regarding time to cardiac mortality or morbidity in cats with first episode of congestive heart failure (CHF) due to primary CMP. ANIMALS: Three hundred and sixty-seven client-owned cats with primary CMP that had presented with a first episode of CHF at 50 centers in Europe. Per-protocol population comprised 193 cats (n = 89 cilobradine, n = 104 placebo). An interim analysis for futility was planned. METHODS: Prospective, randomized, placebo-controlled, double-blinded, multicenter clinical trial. Primary outcome variable was the time to a composite of cardiac mortality or cardiac morbidity. RESULTS: Median time to primary outcome was 84 days (95% confidence interval [CI]: 63-219 days) in the cilobradine group (CG) and 203 days in the placebo group (95% CI: 145-377 days) with observed hazard ratio of 1.44, indicating a higher hazard for the CG (P = 0.057). Mean HR was 28 beats per minute (bpm) lower at Day 7 (P < 0.0001) and remained 29 bpm lower at Day 360 (P = 0.026) in the CG than that in the placebo group. Although the number of adverse events did not differ, there were more serious adverse events in the CG. CONCLUSIONS: Heart rate reduction by cilobradine in cats with a first episode of CHF due to primary CMP did not reduce cardiac mortality and morbidity.
Subject(s)
Cardiomyopathies , Cat Diseases , Heart Failure , Animals , Cats , Benzazepines , Cardiomyopathies/complications , Cardiomyopathies/drug therapy , Cardiomyopathies/veterinary , Cat Diseases/drug therapy , Heart Failure/complications , Heart Failure/drug therapy , Heart Failure/veterinary , Piperidines , Prospective StudiesABSTRACT
BACKGROUND: Changes in clinical variables associated with the administration of pimobendan to dogs with preclinical myxomatous mitral valve disease (MMVD) and cardiomegaly have not been described. OBJECTIVES: To investigate the effect of pimobendan on clinical variables and the relationship between a change in heart size and the time to congestive heart failure (CHF) or cardiac-related death (CRD) in dogs with MMVD and cardiomegaly. To determine whether pimobendan-treated dogs differ from dogs receiving placebo at onset of CHF. ANIMALS: Three hundred and fifty-four dogs with MMVD and cardiomegaly. MATERIALS AND METHODS: Prospective, blinded study with dogs randomized (ratio 1:1) to pimobendan (0.4-0.6 mg/kg/d) or placebo. Clinical, laboratory, and heart-size variables in both groups were measured and compared at different time points (day 35 and onset of CHF) and over the study duration. Relationships between short-term changes in echocardiographic variables and time to CHF or CRD were explored. RESULTS: At day 35, heart size had reduced in the pimobendan group: median change in (Δ) LVIDDN -0.06 (IQR: -0.15 to +0.02), P < 0.0001, and LA:Ao -0.08 (IQR: -0.23 to +0.03), P < 0.0001. Reduction in heart size was associated with increased time to CHF or CRD. Hazard ratio for a 0.1 increase in ΔLVIDDN was 1.26, P = 0.0003. Hazard ratio for a 0.1 increase in ΔLA:Ao was 1.14, P = 0.0002. At onset of CHF, groups were similar. CONCLUSIONS AND CLINICAL IMPORTANCE: Pimobendan treatment reduces heart size. Reduced heart size is associated with improved outcome. At the onset of CHF, dogs treated with pimobendan were indistinguishable from those receiving placebo.
Subject(s)
Cardiotonic Agents/therapeutic use , Mitral Valve Prolapse/drug therapy , Pyridazines/therapeutic use , Animals , Cardiomegaly/drug therapy , Cardiomegaly/veterinary , Dog Diseases/drug therapy , Dogs , Echocardiography/veterinary , Heart Diseases/mortality , Heart Diseases/veterinary , Heart Failure/etiology , Heart Failure/veterinary , Mitral Valve Prolapse/diagnostic imaging , Mitral Valve Prolapse/pathology , Prospective Studies , Quality of LifeABSTRACT
BACKGROUND: Pimobendan is effective in treatment of dogs with congestive heart failure (CHF) secondary to myxomatous mitral valve disease (MMVD). Its effect on dogs before the onset of CHF is unknown. HYPOTHESIS/OBJECTIVES: Administration of pimobendan (0.4-0.6 mg/kg/d in divided doses) to dogs with increased heart size secondary to preclinical MMVD, not receiving other cardiovascular medications, will delay the onset of signs of CHF, cardiac-related death, or euthanasia. ANIMALS: 360 client-owned dogs with MMVD with left atrial-to-aortic ratio ≥1.6, normalized left ventricular internal diameter in diastole ≥1.7, and vertebral heart sum >10.5. METHODS: Prospective, randomized, placebo-controlled, blinded, multicenter clinical trial. Primary outcome variable was time to a composite of the onset of CHF, cardiac-related death, or euthanasia. RESULTS: Median time to primary endpoint was 1228 days (95% CI: 856-NA) in the pimobendan group and 766 days (95% CI: 667-875) in the placebo group (P = .0038). Hazard ratio for the pimobendan group was 0.64 (95% CI: 0.47-0.87) compared with the placebo group. The benefit persisted after adjustment for other variables. Adverse events were not different between treatment groups. Dogs in the pimobendan group lived longer (median survival time was 1059 days (95% CI: 952-NA) in the pimobendan group and 902 days (95% CI: 747-1061) in the placebo group) (P = .012). CONCLUSIONS AND CLINICAL IMPORTANCE: Administration of pimobendan to dogs with MMVD and echocardiographic and radiographic evidence of cardiomegaly results in prolongation of preclinical period and is safe and well tolerated. Prolongation of preclinical period by approximately 15 months represents substantial clinical benefit.
Subject(s)
Cardiomegaly/veterinary , Cardiotonic Agents/therapeutic use , Dog Diseases/drug therapy , Mitral Valve Insufficiency/veterinary , Pyridazines/therapeutic use , Animals , Cardiomegaly/drug therapy , Cardiotonic Agents/adverse effects , Dogs , Female , Heart Failure/drug therapy , Heart Failure/mortality , Heart Failure/veterinary , Male , Mitral Valve Insufficiency/drug therapy , Mitral Valve Insufficiency/mortality , Pyridazines/adverse effectsABSTRACT
BACKGROUND: Left atrial (LA) enlargement, congestive heart failure (CHF), and aortic thromboembolism (ATE) are associated with decreased survival in cats with hypertrophic cardiomyopathy (HCM), but the prognostic value of echocardiographic variables has not been well characterized. HYPOTHESIS/OBJECTIVES: We hypothesized that LA echocardiographic variables and assessment of left ventricular (LV) diastolic and systolic function would have prognostic value in cats with HCM. ANIMALS: Two hundred eighty-two cats diagnosed with HCM. METHODS: Clinical and echocardiographic records of affected cats seen at the Royal Veterinary College from 2004 to 2009 were retrospectively analyzed. Only cats with echocardiographic confirmation of LV diastolic wall thickness ≥ 6 mm were included. Outcomes were obtained from clinical records or referring veterinarians and owners. RESULTS: Deaths occurred in 164 cats, of which 107 were believed to have been cardiac deaths. Univariable predictors of an increased risk of cardiac death included older age, absence of a murmur, presence of a gallop sound or arrhythmia, presentation with either CHF or ATE, extreme LV hypertrophy (≥ 9.0 mm), LV fractional shortening (FS%) ≤ 30%, regional wall hypokinesis, increased left atrial size, decreased left atrial function, spontaneous echo-contrast/thrombus or both, absence of left ventricular outflow tract obstruction, and a restrictive diastolic filling pattern. Cox's proportional hazard analysis identified LA dysfunction, low LV systolic function, and extreme LV hypertrophy as independent predictors of decreased cardiac survival time. CONCLUSIONS AND CLINICAL IMPORTANCE: Echocardiographic measurement of LA function, extreme LV hypertrophy, and LV systolic function provides important prognostic information in cats with HCM.
Subject(s)
Cardiomyopathy, Hypertrophic/veterinary , Cat Diseases/physiopathology , Heart Atria/physiopathology , Heart Failure/veterinary , Thromboembolism/veterinary , Animals , Cardiomyopathy, Hypertrophic/diagnostic imaging , Cardiomyopathy, Hypertrophic/physiopathology , Cat Diseases/diagnostic imaging , Cats , Echocardiography, Doppler/veterinary , Female , Heart Atria/diagnostic imaging , Heart Failure/diagnostic imaging , Heart Failure/physiopathology , Kaplan-Meier Estimate , Male , Multivariate Analysis , Reproducibility of Results , Retrospective Studies , Thromboembolism/diagnostic imaging , Thromboembolism/physiopathologyABSTRACT
OBJECTIVES: To assess the influence of thyroid function on natriuretic peptide concentration in hyperthyroid cats before and after treatment. METHODS: Serum natriuretic peptide concentration was measured in 61 hyperthyroid cats recruited from first-opinion clinics before and after treatment. RESULTS: Following successful treatment, total thyroxine, heart rate, systolic blood pressure and packed cell volume all decreased and bodyweight and creatinine concentrations increased. Furthermore, a significant (P < 0·001) decline in NT-proBNP concentration but not NT-proANP was identified. CLINICAL SIGNIFICANCE: Thyroid function has a modest but significant effect on NT-proBNP concentration. Thyroid status should be taken into account when interpreting NT-proBNP concentrations in cats.
Subject(s)
Cat Diseases/blood , Cats/blood , Hyperthyroidism/veterinary , Natriuretic Peptides/blood , Animals , Antithyroid Agents/therapeutic use , Biomarkers/blood , Blood Pressure/physiology , Case-Control Studies , Cat Diseases/drug therapy , Female , Heart Rate/physiology , Hyperthyroidism/blood , Hyperthyroidism/drug therapy , Male , Methimazole/therapeutic use , Natriuretic Peptide, Brain/blood , Peptide Fragments/blood , Thyroxine/blood , Treatment OutcomeABSTRACT
The records of 11 dogs with evidence of meningoencephalomyelitis of unknown origin were reviewed. Two of them had had a focal form of the disease and the other nine a disseminated form. The forebrain was involved in five of the nine dogs with disseminated disease, the brainstem in all nine and the cerebellum in one. They had been treated with courses of cytosine arabinoside every three weeks and immunosuppressive doses of prednisolone. Their response to the treatment, in terms of quality of life, was judged by their owners and referring veterinarians to have been excellent in five, good in five and poor in one; their survival times ranged from 78 days to more than 603 days. The cumulative probability of survival at two years was 58.4 per cent. No signs of myelosuppression or other side effects associated with cytosine arabinoside were observed.
Subject(s)
Anti-Inflammatory Agents/therapeutic use , Cytarabine/therapeutic use , Dog Diseases/drug therapy , Immunosuppressive Agents/therapeutic use , Meningoencephalitis/veterinary , Prednisolone/therapeutic use , Animals , Cytarabine/adverse effects , Dog Diseases/etiology , Dog Diseases/mortality , Dogs , Drug Therapy, Combination , Female , Male , Meningoencephalitis/drug therapy , Meningoencephalitis/etiology , Meningoencephalitis/mortality , Retrospective Studies , Survival Analysis , Treatment OutcomeSubject(s)
Dust/adverse effects , Respiratory Insufficiency/etiology , Wood , Acute Disease , Adult , Humans , MaleABSTRACT
The results of a survey conducted in a company employing 1850 persons working in air-conditioned premises are reported. One hundred and five persons were examined, including 790 who mostly complained of respiratory disorders and 20 controls. Regular check-ups during the last two years have failed to reveal any serious disease. The most frequent complaints were rhinitis and tracheitis, especially among female employees. No alveolitis was observed. The finding of Bacillus subtilis in samples of ambient air and air-conditioner filters in conjunction with the presence of precipitating antibodies against crude extracts from these samples, suggested that the respiratory disorders might have been due to this microorganism. A multifactorial analysis demonstrated a statistically significant correlation between clinical symptoms and immunological disorders. The air-conditioner disease, therefore, may present as a benign condition.
Subject(s)
Air Conditioning , Occupational Diseases/etiology , Respiratory Tract Diseases/etiology , Adult , Bacillus subtilis/isolation & purification , Female , Humans , Humidity/prevention & control , Male , Occupational Diseases/epidemiology , Respiratory Tract Diseases/epidemiology , Respiratory Tract Diseases/therapy , Respiratory Tract Infections/immunology , Rhinitis/etiology , Tracheitis/etiologySubject(s)
Drug-Related Side Effects and Adverse Reactions , Adolescent , Adult , Aged , Emergency Service, Hospital , Female , Humans , Male , Middle Aged , Patient AdmissionABSTRACT
The authors report their experience of 100 transbronchial pulmonary biopsies done during fibroscopy. The technique is easy; patients with respiratory insufficiency or bullous lesions are excluded. Biopsy is done blindly, without any brillance amplifier. A hundred biopsies were performed (34 in limited opacities, 66 in diffuse images). Pulmonary parenchyma was brought out in 77% of cases and a histological diagnosis was made in 52% of cases. Two pneumothorax and 5 minor hemoptysis occured as sequellae of these biopsies. This method of study is interesting mainly for alveolar or interstitial diffuse pneumopathies. In such cases, it represents a real improvement over the bronchial biopsy, often avoiding the need for a surgical biopsy.
Subject(s)
Biopsy/methods , Bronchoscopy/methods , Lung Diseases/diagnosis , Lung Neoplasms/diagnosis , Biopsy/adverse effects , Fiber Optic Technology , Hemoptysis/etiology , Humans , Lung Diseases/pathology , Lung Neoplasms/pathology , Pneumothorax/etiologyABSTRACT
Starting again a Rifampicin treatment gave rise to an acute renal insufficiency, reversible by hemodialysis. This incident resulted from an immunopathological conflict revealed by the presence of anti-Rifampicin antibodies. Renal needle biopsy did not show any immune deposits. The mechanism of these incidents is discussed. Authors draw attention to the necessity of avoiding discontinuous Rifampicin treatment.