A NEW METHOD TO INCREASE ULTRAFILTRATION IN PERITONEAL DIALYSIS: STEADY CONCENTRATION PERITONEAL DIALYSIS

被引:10
|
作者
Perez-Diaz, Vicente [1 ,2 ]
Perez-Escudero, Alfonso [3 ]
Sanz-Ballesteros, Sandra [1 ]
Rodriguez-Portela, Guadalupe [1 ]
Valenciano-Martinez, Susana [1 ]
Palomo-Aparicio, Sofia [1 ]
Hernandez-Garcia, Esther [4 ]
Sanchez-Garcia, Luisa [5 ]
Gordillo-Martin, Raquel [1 ]
Marcos-Sanchez, Hortensia [6 ]
机构
[1] Hosp Clin Univ Valladolid, Dept Nephrol, Valladolid, Spain
[2] Univ Valladolid, Fac Med, Dept Med, Dermatol & Toxicol, Valladolid, Spain
[3] MIT, Dept Phys, Cambridge, MA 02139 USA
[4] Complejo Asistencial Palencia, Dept Nephrol, Palencia, Spain
[5] Hosp Univ Rio Hortega Valladolid, Dept Nephrol, Valladolid, Spain
[6] Hosp Clin Univ Valladolid, Dept Clin Anal, Valladolid, Spain
来源
PERITONEAL DIALYSIS INTERNATIONAL | 2016年 / 36卷 / 05期
关键词
Ultrafiltration; glucose concentration; fluid overload; technique failure; fluid transport kinetics; osmotic gradient; intraperitoneal pressure; hydrostatic pressure; INTRAPERITONEAL PRESSURE; FILL VOLUME; FLUID; ICODEXTRIN; SOLUTE; ABSORPTION; TRANSPORT; GLUCOSE; VARIABILITY; NUTRITION;
D O I
10.3747/pdi.2016.00007
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Peritoneal dialysis (PD) has limited power for liquid extraction (ultrafiltration), so fluid overload remains a major cause of treatment failure. Methods: We present steady concentration peritonal dialysis (SCPD), which increases ultrafiltration of PD exchanges by maintaining a constant peritoneal glucose concentration. This is achieved by infusing 50% glucose solution at a constant rate (typically 40 mL/h) during the 4-hour dwell of a 2-L 1.36% glucose exchange. We treated 21 fluid overload episodes on 6 PD patients with high or average-high peritoneal transport characteristics who refused hemodialysis as an alternative. Each treatment consisted of a single session with 1 to 4 SCPD exchanges (as needed). Results: Ultrafiltration averaged 653 +/- 363 mL/4 h - twice the ultrafiltration of the peritoneal equilibration test (PET) (300 +/- 251mL/4h, p < 0.001) and 6-fold the daily ultrafiltration (100 +/- 123 mL/4h, p < 0.001). Serum and peritoneal glucose stability and dialysis efficacy were excellent (glycemia 126 +/- 25 mg/dL, peritoneal glucose 1,830 +/- 365 mg/dL, D/P creatinine 0.77 +/- 0.08). The treatment reversed all episodes of fluid overload, avoiding transfer to hemodialysis. Ultrafiltration was proportional to fluid overload (p < 0.01) and inversely proportional to final peritoneal glucose concentration (p < 0.05). Conclusion: This preliminary clinical experience confirms the potential of SCPD to safely and effectively increase ultrafiltration of PD exchanges. It also shows peritoneal transport in a new dynamic context, enhancing the influence of factors unrelated to the osmotic gradient.
引用
收藏
页码:555 / 561
页数:7
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