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Low-Sodium Versus Standard-Sodium Peritoneal Dialysis Solution in Hypertensive Patients: A Randomized Controlled Trial.
Rutkowski, Boleslaw; Tam, Paul; van der Sande, Frank M; Vychytil, Andreas; Schwenger, Vedat; Himmele, Rainer; Gauly, Adelheid.
Afiliação
  • Rutkowski B; Department of Nephrology, Medical University of Gdansk, Gdansk, Poland.
  • Tam P; Scarborough General Hospital, Toronto, Ontario, Canada.
  • van der Sande FM; Division of Nephrology, Department of Internal Medicine, Maastricht University Medical Center, Maastricht, the Netherlands.
  • Vychytil A; Division of Nephrology and Dialysis, Department of Medicine III, Medical University of Vienna, Vienna, Austria.
  • Schwenger V; Department of Nephrology, University of Heidelberg, Heidelberg, Germany.
  • Himmele R; Fresenius Medical Care North America, Waltham, MA.
  • Gauly A; Fresenius Medical Care, Bad Homburg, Germany. Electronic address: adelheid.gauly@fmc-ag.com.
Am J Kidney Dis ; 67(5): 753-61, 2016 May.
Article em En | MEDLINE | ID: mdl-26388284
ABSTRACT

BACKGROUND:

Peritoneal dialysis (PD) solutions with reduced sodium content may have advantages for hypertensive patients; however, they have lower osmolarity and solvent drag, so the achieved Kt/Vurea may be lower. Furthermore, the increased transperitoneal membrane sodium gradient can influence sodium balance with consequences for blood pressure (BP) control. STUDY

DESIGN:

Prospective, randomized, double-blind clinical trial to prove the noninferiority of total weekly Kt/Vurea with low-sodium versus standard-sodium PD solution, with the lower confidence limit above the clinically accepted difference of -0.5. SETTING &

PARTICIPANTS:

Hypertensive patients (≥ 1 antihypertensive drug, including diuretics, or office systolic BP ≥ 130 mmHg) on continuous ambulatory PD therapy from 17 sites. INTERVENTION 108 patients were randomly assigned (11) to 6-month treatments with either low-sodium (125 mmol/L of sodium; 1.5%, 2.3%, or 4.25% glucose; osmolarity, 338-491 mOsm/L) or standard-sodium (134 mmol/L of sodium; 1.5%, 2.3%, or 4.25% glucose; osmolarity, 356-509 mOsm/L) PD solution.

OUTCOMES:

Primary end point weekly total Kt/Vurea; secondary

outcomes:

BP control, safety, and tolerability. MEASUREMENTS Total Kt/Vurea was determined from 24-hour dialysate and urine collection; BP, by office measurement.

RESULTS:

Total Kt/Vurea after 12 weeks was 2.53 ± 0.89 in the low-sodium group (n = 40) and 2.97 ± 1.58 in the control group (n = 42). The noninferiority of total Kt/Vurea could not be confirmed. There was no difference for peritoneal Kt/Vurea (1.70 ± 0.38 with low sodium, 1.77 ± 0.44 with standard sodium), but there was a difference in renal Kt/Vurea (0.83 ± 0.80 with low sodium, 1.20 ± 1.54 with standard sodium). Mean daily sodium removal with dialysate at week 12 was 1.188 g higher in the low-sodium group (P < 0.001). BP changed marginally with standard-sodium solution, but decreased with low-sodium PD solution, resulting in less antihypertensive medication.

LIMITATIONS:

Broader variability of study population than anticipated, particularly regarding residual kidney function.

CONCLUSIONS:

The noninferiority of the low-sodium PD solution for total Kt/Vurea could not be proved; however, it showed beneficial clinical effects on sodium removal and BP.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sódio / Soluções para Hemodiálise / Diálise Peritoneal Ambulatorial Contínua / Hipertensão / Falência Renal Crônica / Anti-Hipertensivos Tipo de estudo: Clinical_trials Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Kidney Dis Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Polônia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sódio / Soluções para Hemodiálise / Diálise Peritoneal Ambulatorial Contínua / Hipertensão / Falência Renal Crônica / Anti-Hipertensivos Tipo de estudo: Clinical_trials Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Kidney Dis Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Polônia