Oct 052011
 

Clinical implications of switching from intensive to moderate statin therapy after acute coronary syndromes.

Int J Cardiol. 2011 Oct 6;152(1):56-60

Authors: Colivicchi F, Tubaro M, Santini M

Abstract
BACKGROUND AND AIMS: Intensive statin therapy represents an effective option after acute coronary syndromes (ACS). Despite evidence, switching to less effective statins frequently occurs in practice. Aim of this observational study was to assess the impact of switching from intensive to moderate statin therapy on clinical outcomes after ACS.
METHODS AND RESULTS: A cohort of 1321 consecutive ACS patients (886 men, age 71±.8years) discharged on atorvastatin 80mg/d in a 6.5year period was followed for 12months after discharge. During follow-up, 557 patients (42%) were switched by primary care physicians to moderate statin therapy, either for side effects (56%) or for safety concerns (44%). No major adverse reaction was reported. Increasing age (HR 1.52 per 10-year increase, 95% CI 1.23-1.78, p=0.01), and female gender (HR 1.11, 95% CI 1.06-1.23, p=0.02) were associated with a higher probability of switch. Patients following a cardiac rehabilitation program (HR 0.64 95% CI 0.49-0.86, p=0.02) and diabetic subjects (HR 0.81, 95% CI 0.67-0.92, p=0.02) were more likely to continue atorvastatin 80mg/d. During follow-up, a major adverse clinical event occurred in 331 patients (one-year probability 0.25, 95% CI 0.22-0.27). Multivariate analysis with Cox proportional hazards method, including statin switching as a time-dependent covariate, demonstrated that, after adjustment for demographic and clinical variables, reduction from intensive to moderate statin therapy was an independent predictor of adverse clinical outcomes (HR 2.7, 95% CI 1.7-5.1, p=0.004).
CONCLUSION: Switching from intensive to moderate statin therapy after ACS is associated with an increased incidence of adverse clinical events.

PMID: 20674999 [PubMed - in process]

Link to Article at PubMed

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Oct 052011
 

A comparison of ST elevation versus non-ST elevation myocardial infarction outcomes in a large registry database Are non-ST myocardial infarctions associated with worse long-term prognoses?

Int J Cardiol. 2011 Oct 6;152(1):70-77

Authors: Polonski L, Gasior M, Gierlotka M, Osadnik T, Kalarus Z, Trusz-Gluza M, Zembala M, Wilczek K, Lekston A, Zdrojewski T, Tendera M,

Abstract
BACKGROUND: Prognoses in STEMI and NSTEMI beyond one year from onset remain unclear. We aimed to compare the treatments and the two-year outcomes in patients with myocardial infarction (MI) enrolled at the Polish Registry of Acute Coronary Syndromes (PL-ACS). METHODS: A total of 13,441 patients with MI (8250 with STEMI, and 5191 with NSTEMI) underwent medical care between October 2003 and June 2005 in the Silesia region (4.8 million inhabitants). The events analyzed were death, MI, stroke and percutaneous (PCI) or surgical (CABG) revascularization. RESULTS: After two years, NSTEMI was associated with a higher incidence of death (hazard ratio (HR) of 1.09 (95% confidence interval (CI) 1.02-1.17, p<0.0001)); a higher incidence of reinfarction, stroke, CABG and a lower rate of PCI. Adjustments for baseline characteristics and treatment strategy (invasive vs. non-invasive) reversed the HR for mortality and eliminated the difference in MI and stroke. The adjusted HR for mortality was 0.76 (95% CI, 0.71-0.83, p<0.0001). STEMI and NSTEMI patients treated non-invasively were older and showed higher incidences of diabetes, obesity, pulmonary edema and cardiogenic shock than their invasively treated counterparts. Invasively treated patients received aspirin, beta-blockers, ACE inhibitors and statins more often during hospitalization and at discharge. CONCLUSIONS: The unadjusted long-term prognosis was worse in NSTEMI. After adjustment for the baseline characteristics and treatment strategy, the long-term prognosis was worse in STEMI. Patients with MI treated invasively showed more favorable clinical characteristics and received guideline-recommended therapy more often than patients who did not undergo invasive treatment.

PMID: 20684999 [PubMed - as supplied by publisher]

Link to Article at PubMed

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Oct 052011
 

Does modifying electrode placement of the 12 lead ECG matter in healthy subjects?

Int J Cardiol. 2011 Oct 20;152(2):184-91

Authors: Sheppard JP, Barker TA, Ranasinghe AM, Clutton-Brock TH, Frenneaux MP, Parkes MJ

Abstract
BACKGROUND: Limb electrodes for the 12 lead ECG are routinely placed on the torso during exercise stress testing or when limbs are clinically inaccessible. It is unclear whether such electrode modification produces ECG changes in healthy male or female subjects that are clinically important according to the 2009 AHA, ACCF, HRS guidelines. We therefore measured whether ECG modification produced clinically important or false positive ECG changes e.g., appearance of Q waves in leads V(1-3), ST changes greater than 0.1mV, T wave changes greater than 0.5mV (frontal plane) or 1mV (transverse plane), QRS axis shifts or alterations to QTc/P-R/QRS intervals.
METHODS: The 12 lead ECG was measured in 18 healthy and semi-recumbent subjects using the standard and Takuma modified limb placements.
RESULTS: In the frontal plane we demonstrate that the modification of limb electrode placement produces small Q, R and T wave amplitude and QRS axis changes that are statistically but not clinically significant. In the transverse plane it produces no statistically or clinically significant changes in the ECG or in ST segment morphology, P-R, QRS or QTc intervals.
CONCLUSIONS: We provide better and more robust evidence that routine modification of limb electrode placement produces only minor changes to the ECG waveform in healthy subjects. These are not clinically significant according to the 2009 guidelines and thus have no effect on the clinical specificity of the 12 lead ECG.

PMID: 20701990 [PubMed - in process]

Link to Article at PubMed

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Oct 052011
 

Effects of levosimendan on mortality and hospitalization. A meta-analysis of randomized controlled studies.

Crit Care Med. 2011 Sep 29;

Authors: Landoni G, Biondi-Zoccai G, Greco M, Greco T, Bignami E, Morelli A, Guarracino F, Zangrillo A

Abstract
OBJECTIVE:: Catecholaminergic inotropes have a place in the management of low output syndrome and decompensated heart failure but their effect on mortality is debated. Levosimendan is a calcium sensitizer that enhances myocardial contractility without increasing myocardial oxygen use. A meta-analysis was conducted to determine the impact of levosimendan on mortality and hospital stay. DATA SOURCES:: BioMedCentral, PubMed, Embase, and the Cochrane Central Register of clinical trials were searched for pertinent studies. International experts and the manufacturer were contacted. STUDY SELECTION:: Articles were assessed by four trained investigators, with divergences resolved by consensus. Inclusion criteria were random allocation to treatment and comparison of levosimendan vs. control. There were no restrictions on dose or time of levosimendan administration or on language. Exclusion criteria were: duplicate publications, nonadult studies, oral administration of levosimendan, and no data on main outcomes. DATA EXTRACTION:: Study end points, main outcomes, study design, population, clinical setting, levosimendan dosage, and treatment duration were extracted. DATA SYNTHESIS:: Data from 5,480 patients in 45 randomized clinical trials were analyzed. The overall mortality rate was 17.4% (507 of 2915) among levosimendan-treated patients and 23.3% (598 of 2565) in the control group (risk ratio = 0.80 [0.72; 0.89], p for effect < .001, number needed to treat = 17 with 45 studies included). Reduction in mortality was confirmed in studies with placebo (risk ratio = 0.82 [0.69; 0.97], p = .02) or dobutamine (risk ratio = 0.68 [0.52-0.88]; p = .003) as comparator and in studies performed in cardiac surgery (risk ratio = 0.52 [0.35; 0.76] p = .001) or cardiology (risk ratio = 0.75 [0.63; 0.91], p = .003) settings. Length of hospital stay was reduced in the levosimendan group (weighted mean difference = -1.31 [-1.95; -0.31], p for effect = .007, with 17 studies included). A trend toward a higher percentage of patients experiencing hypotension was noted in levosimendan vs. control (risk ratio = 1.39 [0.97-0.1.94], p = .053). CONCLUSIONS:: Levosimendan might reduce mortality in cardiac surgery and cardiology settings of adult patients.

PMID: 21963578 [PubMed - as supplied by publisher]

Link to Article at PubMed

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Oct 052011
 

Neglect of quality-of-life considerations in intensive care unit family meetings for long-stay intensive care unit patients.

Crit Care Med. 2011 Sep 29;

Authors: Douglas SL, Daly BJ, Lipson AR

Abstract
OBJECTIVE:: To examine the frequency with which quality of life and treatment limitation were discussed in formal family meetings for long-stay intensive care unit patients with high risk for mortality and morbidity. DESIGN:: Descriptive observational study. SETTING:: Five intensive care units. PATIENTS:: One hundred sixteen family surrogate decisionmakers of long-stay intensive care unit patients who participated in an intensive communication system that aimed to provide weekly meetings with family decisionmakers. The structure of each meeting was to address medical update, patient preferences, treatment plan, and milestones for evaluating the treatment plan. INTERVENTIONS:: None. MEASUREMENTS AND MAIN RESULTS:: We audiotaped initial family meetings for 116 family decisionmakers for a total of 180 meetings. On average, meetings were 24 mins long with a majority of time being devoted to nonemotional speech and little (12%) spent discussing patient preferences. Quality of life was discussed in 45% and treatment limitation in 23% of all meetings. Quality-of-life discussions were more likely to occur when patients were admitted to a medical intensive care unit (odds ratio [OR], 5.9; p = .005), have a family decisionmaker who is a spouse (OR, 9.4; p = .0001), were older (OR, 1.04; p = 01), have a shorter length of stay (OR, 0.93; p = .001), and have a family decisionmaker who was a spouse (OR, 5.1; p = .002). For those with a treatment limitation discussion, 67% had a do-not-resuscitation order, 40% were admitted to a medical intensive care unit, 56% had a family decisionmaker who had been their caregiver, and 48% of their family decisionmakers were their children. CONCLUSIONS:: To guide discussion with families of the subset of intensive care unit patients with high risk of mortality and long-term morbidity, quality of life was not consistently addressed. Continued efforts to assist clinicians in routinely including discussions of quality-of-life outcomes is needed.

PMID: 21963580 [PubMed - as supplied by publisher]

Link to Article at PubMed

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Oct 052011
 

Evaluation of screening risk and nonrisk patients for methicillin-resistant Staphylococcus aureus on admission in an acute care hospital.

Am J Infect Control. 2011 Sep 30;

Authors: Creamer E, Galvin S, Dolan A, Sherlock O, Dimitrov BD, Fitzgerald-Hughes D, Thomas T, Walsh J, Moore J, Smyth EG, Shore AC, Sullivan D, Kinnevey P, O'Lorcain P, Cunney R, Coleman DC, Humphreys H

Abstract
BACKGROUND: Screening for methicillin-resistant Staphylocccus aureus (MRSA) is advocated as part of control measures, but screening all patients on admission to hospital may not be cost-effective. OBJECTIVE: Our objective was to evaluate the additional yield of screening all patients on admission compared with only patients with risk factors and to assess cost aspects. METHODS: A prospective, nonrandomized observational study of screening nonrisk patients ?72 hours of admission compared with only screening patients with risk factors over 3 years in a tertiary referral hospital was conducted. We also assessed the costs of screening both groups. RESULTS: A total of 48 of 892 (5%) patients was MRSA positive; 28 of 314 (9%) during year 1, 12 of 257 (5%) during year 2, and 8 of 321 (2%) during year 3. There were significantly fewer MRSA-positive patients among nonrisk compared with MRSA-risk patients: 4 of 340 (1%) versus 44 of 552 (8%), P ? .0001, respectively. However, screening nonrisk patients increased the number of screening samples by 62% with a proportionate increase in the costs of screening. A backward stepwise logistic regression model identified age > 70 years, diagnosis of chronic pulmonary disease, previous MRSA infection, and admission to hospital during the previous 18 months as the most important independent predictors to discriminate between MRSA-positive and MRSA-negative patients on admission (94.3% accuracy, P < .001). CONCLUSION: Screening patients without risk factors increased the number of screenings and costs but resulted in few additional cases being detected. In a hospital where MRSA is endemic, targeted screening of at-risk patients on admission remains the most efficient strategy for the early identification of MRSA-positive patients.

PMID: 21962934 [PubMed - as supplied by publisher]

Link to Article at PubMed

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