82 research outputs found
Clinical features and outcomes of elderly hospitalised patients with chronic obstructive pulmonary disease, heart failure or both
Background and objective: Chronic obstructive pulmonary disease (COPD) and heart failure (HF) mutually increase the risk of being present in the same patient, especially if older. Whether or not this coexistence may be associated with a worse prognosis is debated. Therefore, employing data derived from the REPOSI register, we evaluated the clinical features and outcomes in a population of elderly patients admitted to internal medicine wards and having COPD, HF or COPD + HF. Methods: We measured socio-demographic and anthropometric characteristics, severity and prevalence of comorbidities, clinical and laboratory features during hospitalization, mood disorders, functional independence, drug prescriptions and discharge destination. The primary study outcome was the risk of death. Results: We considered 2,343 elderly hospitalized patients (median age 81 years), of whom 1,154 (49%) had COPD, 813 (35%) HF, and 376 (16%) COPD + HF. Patients with COPD + HF had different characteristics than those with COPD or HF, such as a higher prevalence of previous hospitalizations, comorbidities (especially chronic kidney disease), higher respiratory rate at admission and number of prescribed drugs. Patients with COPD + HF (hazard ratio HR 1.74, 95% confidence intervals CI 1.16-2.61) and patients with dementia (HR 1.75, 95% CI 1.06-2.90) had a higher risk of death at one year. The Kaplan-Meier curves showed a higher mortality risk in the group of patients with COPD + HF for all causes (p = 0.010), respiratory causes (p = 0.006), cardiovascular causes (p = 0.046) and respiratory plus cardiovascular causes (p = 0.009). Conclusion: In this real-life cohort of hospitalized elderly patients, the coexistence of COPD and HF significantly worsened prognosis at one year. This finding may help to better define the care needs of this population
Cardiac autonomic dysfunction is associated with white matter lesions in patients with MCI
Background. Cardiac autonomic dysfunction has been associated with cognitive impairment, but the underlying
pathogenesis is complex and cerebral white matter lesions (WMLs) might be implicated.
Methods. Time and frequency heart rate variability (HRV) and visual rating of WMLs were carried out in 42 patients
with mild cognitive impairment.
Results. After adjustment for relevant demographic and clinical characteristics, including left ventricular mass, reduced
HRV indices of parasympathetic (root mean square of successive difference of RR intervals, RMSSD) and sympathetic
modulation (low-frequency [LF] power) were associated with increased WML score (RMSSD: B − 0.30, 95%
CI − 0.52 to − 0.08, p = .01; LF: B − 0.24, 95% CI − 0.46 to − 0.02, p = .05). In a multiple-adjusted model, RMSSD was the
major independent predictor of WMLs ( B − 0.35, 95% CI − 0.57 to − 0.13, p = .002).
Conclusion. The evidence for an independent association of cardiac autonomic dysfunction with WMLs might
suggest its role in the pathogenesis of WMLs
Picotamide, a dual TXB synthetase inhibitor and TXB receptor antagonist, reduces exercise-induced albuminuria in microalbuminuric patients with NIDDM.
Association of blood pressure and genetic background with white matter lesions in patients with mild cognitive impairment.
Background. White matter lesions (WMLs) may contribute to cognitive deficits in patients with mild cognitive
impairment (MCI), but their pathogenesis is complex. Fluctuations of blood pressure (BP) over 24 hours and genetic
predisposition to develop vascular damage have been implicated.
Methods. In 63 MCI patients 65 years old or older, BP was measured both clinically and with ambulatory BP
monitoring. Patients were classified in two groups: no/very mild (n ¼ 34) and mild to severe (n ¼ 29) WMLs, based on
a visual scale on magnetic resonance (mean age 71.8 6 4.7 vs 74.6 6 5.1, and female gender 53% vs 66%, respectively).
The volume of WMLs was measured by a semi-automatic method, separately for periventricular caps and rim,
periventricular confluent, subcortical punctate, and subcortical confluent. Polymorphisms of cystatin C (CST3) and
cholesterol 24-hydroxylase (CYP46) genes, putative risk factors for cerebrovascular disease, were determined.
Results. The prevalence of cerebrovascular risk factors was similar in the two MCI groups of different WML severity,
as well as clinic and ambulatory BP. In patients with mild to severe, but not in those with no/very mild WMLs, the volume
of periventricular confluent WMLs increased with increasing daytime systolic BP (regression coefficient .47, 95%
confidence interval [CI], .13 to .71 vs .02, 95% CI,.32 to .36, p¼.003 for the difference between slopes). The volume of
other WML subtypes was not associated with ambulatory BP. Participants carrying both CST3*B and CYP46*T alleles
were overrepresented in the MCI group with mild to severe WMLs (43% vs 17%, p .03).
Conclusions. BP and gene putative risk factors for cerebrovascular disease are differentially associated with WMLs in
two MCI groups of different WML severity. WMLs might develop for the convergence of innate with acquired factors
Multicenter randomized trial comparing meropenem (1.5 gr daily) and imipienem/cilastatin (2 g daily) in the hospital treatment of community-acquired pneumonia.
Single-access-laparoscopy and foregut-surgery from Giovanni Dapri
SCOPUS: ch.binfo:eu-repo/semantics/publishe
Consensus Document on substitution therapy with DHEA in the elderly. GISEG (Italian Study Group on Geriatric Endocrinology),
CONSENSUS DOCUMENT ON SUBSTITUTION THERAPY WITH DHEA IN THE ELDERLY
In this Consensus Document on substitution therapy with DHEA in the elderly we examine: the age-correlated decline, the mechanism of action and the biochemical assessment of dehydroepiandrosterone both in males and females; the potential biological effects of DHEA on the the different systems, functions and metabolisms in the elderly; the potential side effects of DHEA substitution therapy; the available preparations of DHEA. Eventually we suggest some final recommendations about DHEA
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