PERITONEAL TRANSPORT IN CAPD PATIENTS WITH PERMANENT LOSS OF ULTRAFILTRATION CAPACITY

被引:279
作者
HEIMBURGER, O
WANIEWSKI, J
WERYNSKI, A
TRANAEUS, A
LINDHOLM, B
机构
[1] KAROLINSKA INST,HUDDINGE UNIV HOSP,CTR CLIN RES,S-10401 STOCKHOLM 60,SWEDEN
[2] INST BIOCYBERNET & BIOMED ENGN,WARSAW,POLAND
关键词
D O I
10.1038/ki.1990.231
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
During a 10 year period, 14 out of 227 patients (6.2%) undergoing continuous ambulatory peritoneal dialysis (CAPD) developed permanent loss of ultrafiltration capacity (UFC). The risk of UFC loss increased from 2.6% after one year to 30.9% after six years of treatment. A six hour, single dwell study with glucose 3.86% dialysis fluid was carried out in nine of the UFC loss patients and in 18 CAPD patients with normal UFC. Intraperitoneal dialysate volumes were calculated using 131I-tagged albumin (RISA) as volume marker with a correction applied for its elimination from the peritoneal cavity. The RISA elimination coefficient (KE), which can serve as an estimation of the upper limit of the lymphatic flow, was also calculated. Diffusive mass transport coefficients (KBD) for investigated solutes (glucose, creatinine, urea, potassium, total protein, albumin and β2-microglobulin) were calculated during a period of dialysate isovolemia. Two patterns of UFC loss were observed: (a) seven patients had high KBD values for small solutes resulting in rapid uptake of glucose, whereas KBD values for proteins were normal; (b) two patients had normal KBD values but a threefold increase both in the fluid reabsorption rate and KE. We conclude that loss of the osmotic driving force (due to increased diffusive mass transport for small solutes) and increased fluid reabsorption (possibly due to increased lymphatic reabsorption) are the two major causes of permanent loss of UFC in CAPD patients.
引用
收藏
页码:495 / 506
页数:12
相关论文
共 63 条
  • [1] RESTORATION OF ULTRAFILTRATION CAPACITY OF PERITONEAL MEMBRANE IN PATIENTS ON CAPD
    BAZZATO, G
    COLI, U
    LANDINI, S
    LUCATELLO, S
    FRACASSO, A
    RIGHETTO, F
    SCANFERLA, F
    MORACHIELLO, P
    [J]. INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS, 1984, 7 (02) : 93 - 96
  • [2] BREBOROWICZ A, 1987, PERITON DIALYSIS INT, V7, P6
  • [3] CANTALUPPI A, 1986, ADV CONTINUOUS AMBUL, P12
  • [4] PHOSPHATIDYLCHOLINE AND PERITONEAL TRANSPORT DURING PERITONEAL-DIALYSIS
    DIPAOLO, N
    BUONCRISTIANI, U
    CAPOTONDO, L
    GAGGIOTTI, E
    DEMIA, M
    ROSSI, P
    SANSONI, E
    BERNINI, M
    [J]. NEPHRON, 1986, 44 (04): : 365 - 370
  • [5] FALLER B, 1984, PERITON DIALYSIS B, V4, P10
  • [6] Flessner M F, 1989, ASAIO Trans, V35, P178, DOI 10.1097/00002480-198904000-00016
  • [7] EXCHANGE OF MACROMOLECULES BETWEEN PERITONEAL-CAVITY AND PLASMA
    FLESSNER, MF
    DEDRICK, RL
    SCHULTZ, JS
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 248 (01): : H15 - H25
  • [8] PERITONEAL LYMPHATIC UPTAKE OF FIBRINOGEN AND ERYTHROCYTES IN THE RAT
    FLESSNER, MF
    PARKER, RJ
    SIEBER, SM
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1983, 244 (01): : H89 - H96
  • [9] GOKAL R, 1987, LANCET, V2, P1105
  • [10] HALLETT MD, 1989, PERITONEAL DIALYSIS, P380