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1.
Crit Care ; 16(2): R43, 2012 Mar 09.
Article in English | MEDLINE | ID: mdl-25927574

ABSTRACT

INTRODUCTION: Despite evidence-based guidelines for venous thromboembolism prevention, substantial variability is found in practice. Many economic evaluations of new drugs for thromboembolism prevention do not occur prospectively with efficacy studies and are sponsored by the manufacturers, raising the possibility of bias. We performed a systematic review of economic analyses of venous thromboembolism prevention in hospitalized patients to inform clinicians and policy makers about cost-effectiveness and the potential influence of sponsorship. METHODS: We searched MEDLINE, EMBASE, Cochrane Databases, ACP Journal Club, and Database of Abstracts of Reviews of Effects, from 1946 to September 2011. We extracted data on study characteristics, quality, costs, and efficacy. RESULTS: From 5,180 identified studies, 39 met eligibility and quality criteria. Each addressed pharmacologic prevention: low-molecular-weight heparins versus placebo (five), unfractionated heparin (12), warfarin (eight), one or another agents (five); fondaparinux versus enoxaparin (11); and rivaroxaban and dabigatran versus enoxaparin (two). Low-molecular-weight heparins were most economically attractive among most medical and surgical patients, whereas fondaparinux was favored for orthopedic patients. Fondaparinux was associated with increased bleeding events. Newer agents rivaroxaban and dabigatran may offer additional value. Of all economic evaluations, 64% were supported by manufacturers of a "new" agent. The new agent had a favorable outcome in 38 (97.4%) of 39 evaluations [95% confidence interval [CI] (86.5 to 99.9)]. Among studies supported by a pharmaceutical company, the sponsored medication was economically attractive in 24 (96.0%) of 25 [95% CI, 80.0 to 99.9)]. We could not detect a consistent bias in outcome based on sponsorship; however, only a minority of studies were unsponsored. CONCLUSION: Low-molecular-weight heparins and fondaparinux are the most economically attractive drugs for venous thromboembolism prevention in hospitalized patients. Approximately two thirds of evaluations were supported by the manufacturer of the new agent; such drugs were likely to be reported as economically favorable.


Subject(s)
Anticoagulants/therapeutic use , Enoxaparin/therapeutic use , Heparin, Low-Molecular-Weight/therapeutic use , Hospitalization/economics , Polysaccharides/therapeutic use , Practice Guidelines as Topic , Venous Thromboembolism/economics , Cost-Benefit Analysis , Enoxaparin/administration & dosage , Fondaparinux , Heparin, Low-Molecular-Weight/administration & dosage , Humans , Polysaccharides/administration & dosage , Venous Thromboembolism/drug therapy , Venous Thromboembolism/prevention & control
2.
J Am Diet Assoc ; 109(8): 1406-10, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19631047

ABSTRACT

The impact of heart failure and its treatment on specific nutrient requirements is unknown. Furthermore, depletion of water-soluble B vitamins that play key roles in the production of cellular energy in patients with heart failure can contribute to depletion of energy reserves observed in the failing heart. A cross-sectional study recently reported that approximately one third of hospitalized patients with heart failure had tissue levels suggestive of thiamin deficiency (vitamin B-1). Riboflavin (vitamin B-2) and pyridoxine (vitamin B-6) are similar to thiamin in that they are water-soluble, subject to renal excretion, have limited tissue storage, and are dependent on intake. Therefore, it was hypothesized that the status of these B vitamins may also be adversely affected by heart failure. As a result, the prevalence of patients at risk of vitamin B-2 (erythrocyte glutathione reductase activity coefficient > or = 1.2) and B-6 deficiency (plasma B-6 < or = 20 nmol/L) was determined in a cross-section of 100 patients hospitalized with heart failure between April 2001 and June 2002 as well as in a group of volunteers without heart failure. Twenty-seven percent of patients with heart failure had biochemical evidence of vitamin B-2 deficiency, while 38% had evidence of B-6 deficiency. These prevalence rates were significantly higher than those observed in the volunteers without heart failure (2% and 19%, respectively; P < or = 0.02). Use of common B-vitamin-containing supplements by patients with heart failure did not significantly reduce deficiency rates in comparison with those who did not use supplements (B-2 P=0.38 or B-6 P=0.18)). Finally, while 80% of patients with heart failure took diuretics, neither the dose nor the duration of furosemide use was related to the presence of either B-2 or B-6 deficiency. Given the physiologic importance of these vitamins, further investigations aimed at determining the effect of heart failure on specific nutrient requirements as well as the safety and efficacy of B-vitamin supplementation are warranted.


Subject(s)
Heart Failure/blood , Nutritional Requirements , Nutritional Status , Riboflavin Deficiency/epidemiology , Vitamin B 6 Deficiency/epidemiology , Aged , Chi-Square Distribution , Cross-Sectional Studies , Dietary Supplements , Female , Heart Failure/epidemiology , Heart Failure/etiology , Hospitalization , Humans , Logistic Models , Male , Middle Aged , Odds Ratio , Ontario/epidemiology , Prevalence , Riboflavin/administration & dosage , Riboflavin/blood , Riboflavin Deficiency/blood , Riboflavin Deficiency/drug therapy , Risk Factors , Statistics, Nonparametric , Thiamine/administration & dosage , Thiamine/blood , Thiamine Deficiency/blood , Thiamine Deficiency/drug therapy , Thiamine Deficiency/epidemiology , Vitamin B 6/administration & dosage , Vitamin B 6/blood , Vitamin B 6 Deficiency/blood , Vitamin B 6 Deficiency/drug therapy
3.
Br J Hosp Med (Lond) ; 68(9): 477-81, 2007 Sep.
Article in English | MEDLINE | ID: mdl-17953297

ABSTRACT

Patients who survive critical illness are at risk of permanent physical and functional deficits which decrease the health-related quality of life. The reasons for physical morbidity include the nature of and treatment for the inciting critical illness, new decrements in organ function and worsening of pre-existing organ dysfunction, and prolonged physical immobility and long intensive care unit stay.


Subject(s)
Critical Care , Critical Illness/therapy , Quality of Life , Cachexia/etiology , Critical Care/standards , Exercise Tolerance , Humans , Muscle Weakness/etiology , Respiratory Distress Syndrome/physiopathology , Respiratory Distress Syndrome/therapy , Survivors
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