PMID- 17992382 OWN - NLM STAT- MEDLINE DCOM- 20080718 LR - 20190606 IS - 1678-4170 (Electronic) IS - 0066-782X (Linking) VI - 89 IP - 4 DP - 2007 Oct TI - Hypertonic saline solution for renal failure prevention in patients with decompensated heart failure. PG - 251-5 AB - BACKGROUND: Hyponatremia and congestive phenomena indicate a bad prognosis in decompensated heart failure. The occurrence of renal failure is associated to an increased death risk. OBJECTIVE: To evaluate the safety and efficacy of the hypertonic saline solution in patients with decompensated heart failure for renal failure prevention. METHODS: Patients with decompensated heart failure, congestion and hyponatremia participated in the study. In addition to the standard treatment, the patients received hypertonic saline solution and were submitted to clinical as well as laboratory assessment. RESULTS: Nine patients were enrolled in the study. Mean age was 55 + 14.2 years, being 5 male (55.5%) and 4 (44.5%) female patients. All of them presented functional class III-IV of the New York Heart Association (NYHA), and 5 (55.5%) received dobutamine. All of them presented initial creatinine > 1.4 mg/dl. The mean tonicity of the solution was 4.39% + 0.018% (2.5% to 7.5%) and the duration of treatment was 4.9 days + 4.1 days (1-15 days). There were no severe adverse effects; none of the patients presented clinical worsening or neurologic disorders; hypokalemia occurred in 4 cases (44.5%). The comparison of the variables before and after treatment showed a decrease in urea (105 mg/dl + 74.8 mg/dl vs. 88 mg/dl + 79.4 mg/dl; p = 0.03) and increase in the urinary volume (1,183 ml/day vs. 1,778 ml/day; p = 0.03); there was no tendency to creatinine decrease (2.0 mg/dl + 0.8 mg/dl vs. 1.7 mg/dl + 1.0 mg/dl; p = 0.08). Despite the elevation in sodium levels (131 mEq/l + 2.8 mEq/l vs. 134 mEq/l + 4.9 mEq/l) and weight decrease (69.5 kg + 18.6 kg vs. 68.2 kg + 17.1 kg), there was no statistically significant difference. CONCLUSION: The use of hypertonic saline solution in patients with decompensated heart failure can be a safe therapeutic method and potentially related to clinical improvement and renal failure prevention. FAU - Issa, Victor Sarli AU - Issa VS AD - Instituto do Coracao, Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, Brasil. victorissa@cardiol.br FAU - Bacal, Fernando AU - Bacal F FAU - Mangini, Sandrigo AU - Mangini S FAU - Carneiro, Rodrigo Moreno Dias AU - Carneiro RM FAU - Azevedo, Cristiano Humberto Naves de Freitas AU - Azevedo CH FAU - Chizzola, Paulo Roberto AU - Chizzola PR FAU - Ferreira, Silvia Moreira Ayub AU - Ferreira SM FAU - Bocchi, Edimar Alcides AU - Bocchi EA LA - eng LA - por PT - Clinical Trial PT - Journal Article PL - Brazil TA - Arq Bras Cardiol JT - Arquivos brasileiros de cardiologia JID - 0421031 RN - 0 (Biomarkers) RN - 0 (Cardiotonic Agents) RN - 0 (Diuretics) RN - 0 (Saline Solution, Hypertonic) RN - 3S12J47372 (Dobutamine) RN - 7LXU5N7ZO5 (Furosemide) RN - 8W8T17847W (Urea) RN - 9NEZ333N27 (Sodium) RN - AYI8EX34EU (Creatinine) RN - RWP5GA015D (Potassium) SB - IM MH - Biomarkers/blood MH - Cardiotonic Agents/therapeutic use MH - Creatinine/blood MH - Diuretics/therapeutic use MH - Dobutamine/therapeutic use MH - Female MH - Furosemide/therapeutic use MH - Heart Failure/blood/*drug therapy MH - Humans MH - Hypokalemia/etiology MH - Hyponatremia/blood/*drug therapy MH - Male MH - Middle Aged MH - Potassium/blood MH - Renal Insufficiency/*prevention & control MH - Saline Solution, Hypertonic/adverse effects/*therapeutic use MH - Severity of Illness Index MH - Sodium/blood MH - Time Factors MH - Treatment Outcome MH - Urea/blood EDAT- 2007/11/10 09:00 MHDA- 2008/07/19 09:00 CRDT- 2007/11/10 09:00 PHST- 2006/12/12 00:00 [received] PHST- 2007/04/16 00:00 [accepted] PHST- 2007/11/10 09:00 [pubmed] PHST- 2008/07/19 09:00 [medline] PHST- 2007/11/10 09:00 [entrez] AID - S0066-782X2007001600007 [pii] AID - 10.1590/s0066-782x2007001600007 [doi] PST - ppublish SO - Arq Bras Cardiol. 2007 Oct;89(4):251-5. doi: 10.1590/s0066-782x2007001600007.