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Clinical |
Department of Medicine, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong, China
Correspondence to: C.C. Szeto, Department of Medicine & Therapeutics, Prince of Wales Hospital, Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China. ccszeto{at}cuhk.edu.hk
Objective: Cardiovascular disease (CVD) is the most
common cause of mortality in chronic peritoneal dialysis (PD) patients.
Increased arterial stiffness may be related to a high peritoneal permeability
resulting in fluid overload in PD patients. We studied the relations between
arterial stiffness, peritoneal transport, and radiographic parameters of
systemic fluid overload in a cohort of Chinese PD patients.
Design: Prospective cohort study.
Setting: University referral center.
Patients: We studied 107 PD patients. Vascular pedicle
width and cardiothoracic ratio were measured from a plain postero-anterior
chest radiograph. Pulse wave velocity (PWV) was determined at
carotid–femoral (C-F) and carotid–radial sites. Peritoneal
transport was determined by the dialysate-to-plasma ratio (D/P) of creatinine
at 4 hours of dwell. Patients were followed for 9.4 ± 4.6
months.
Outcome Measures: Duration of hospitalization;
actuarial and technique survival.
Results: There were no relationships between
radiographic measures, arterial PWV, and D/P creatinine. However, both C-F PWV
and D/P creatinine were independent predictors of the number of
hospitalizations for CVD. None of the parameters correlated with mortality in
this study.
Conclusions: There were no relationships between
radiological parameters of fluid overload, peritoneal transport
characteristics, and arterial PWV. Both C-F PWV and D/P creatinine were
independent predictors of the number of hospitalizations for CVD. Our result
suggests that arterial stiffness and high peritoneal transport each contribute
to the development of CVD in this group of patients.
KEY WORDS: Vascular pedicle width; cardiothoracic ratio; pulse wave velocity; peritoneal transport characteristics; cardiovascular disease.
Received 9 December 2008; accepted 25 March 2009.
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