دورية أكاديمية

Meta-Analysis: Low-Dose Dopamine Increases Urine Output but Does Not Prevent Renal Dysfunction or Death.

التفاصيل البيبلوغرافية
العنوان: Meta-Analysis: Low-Dose Dopamine Increases Urine Output but Does Not Prevent Renal Dysfunction or Death.
المؤلفون: Friedrich, Jan O., Adhikari, Neill, Herridge, Margaret S., Beyene, Joseph
المصدر: Annals of Internal Medicine; 4/5/2005, Vol. 142 Issue 7, p510-W-86, 22p
مصطلحات موضوعية: DOPAMINE, URINE, KIDNEY diseases, CREATINE, BIOGENIC amines, CATECHOLAMINES
مستخلص: Background: Surveys have documented the continued popularity of low-dose dopamine to influence renal dysfunction even though few data support it and editorials and reviews have discouraged its use. Purpose: To evaluate the effects of low-dose dopamine (⩽5 μg/kg of body weight per minute) compared with placebo or no therapy in patients with or at risk for acute renal failure. Data Sources: MEDLINE (1966-January 2005), EMBASE (1980-week 5, 2005), CANCERLIT (1975-2002), CINAHL (1982-January 2005), and CENTRAL (The Cochrane Library, fourth quarter, 2004); bibliographies of retrieved publications; and additional information from 50 trials. Study Selection: Two reviewers independently selected parallelgroup randomized and quasi-randomized controlled trials of lowdose dopamine versus control. Data Extraction: Study methods, clinical and renal physiologic outcomes, and adverse events (arrhythmias and myocardial, limb, and cutaneous ischemia) were extracted. Data Synthesis: 61 trials that randomly assigned 3359 patients were identified. Meta-analyses using random-effects models showed no effect of low-dose dopamine on mortality (relative risk, 0.96 [95% CI, 0.78 to 1.19]), need for renal replacement therapy (relative risk, 0.93 [CI, 0.76 to 1.15]), or adverse events (relative risk, 1.13 [CI, 0.90 to 1.41]). Low-dose dopamine increased urine output by 24% (CI, 14% to 35%) on day 1. Improvements in serum creatinine level (4% relative decrease [CI, 1% to 7%]) and measured creatinine clearance (6% relative increase [CI, 1% to 11%]) on day 1 were clinically insignificant. There were no significant changes on days 2 and 3 of therapy. Limitations: Statistically significant between-study heterogeneity in physiologic but not clinical outcomes was unexplained by prespecified hypotheses. Conclusion: Low-dose dopamine offers transient improvements in renal physiology, but no good evidence shows that it offers important clinical benefits to patients with or at risk for acute renal failure. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:00034819
DOI:10.7326/0003-4819-142-7-200504050-00010