Key result
Peritoneal dialysis exchange triggers regional wall motion abnormalities in only ~5% of myocardial segments.
Why the study?
Hemodynamic changes during hemodialysis can cause subclinical myocardial ischemia, but it is unclear if peritoneal dialysis induces similar myocardial ischemia.
Does a peritoneal dialysis exchange induce subclinical myocardial ischemia in patients on peritoneal dialysis?
Observational (n=10)
Does a peritoneal dialysis exchange induce subclinical myocardial ischemia in patients on peritoneal dialysis?
Unlike hemodialysis, peritoneal dialysis exchange does not induce acute subclinical myocardial ischemia, as evidenced by a lack of regional wall motion abnormalities and improved shortening fraction.
Supports safety of peritoneal dialysis exchanges regarding acute ischemia; leaves open confirmation in randomized trials.
BACKGROUND: Hemodynamic changes during hemodialysis can precipitate subclinical myocardial ischemia, which over time contributes to the development of cardiac failure and is associated with a poor prognosis. Peritoneal dialysis (PD) is also associated with acute changes in systemic hemodynamics and a similarly high incidence of cardiovascular disease; we therefore sought to examine whether the hemodynamic effects of a PD exchange would be sufficient to induce subclinical myocardial ischemia. METHODS: 10 patients on PD entered a prospective observational study to determine whether left ventricular (LV) regional wall motion abnormalities (RWMAs) developed following a dialysate exchange. Serial echocardiography with quantitative analysis was used to assess ejection fraction and regional systolic LV function (shortening fraction). Blood pressure (BP) and hemodynamic variables were measured using continuous pulse wave analysis. RESULTS: We observed a very low frequency of RWMA development (5/100 regions). Only 1 patient had more than 1 RWMA and 6 patients were entirely unaffected. Overall mean shortening fraction increased when comparing pre and post values for both 2-chamber (from 3.06% ± 1.5% to 4.26% ± 1.3%, p = 0.001) and 4-chamber (from 3.00% ± 0.7% to 3.67% ± 0.9%, p = 0.021) analyses. Mean arterial pressure fell by a small degree during drainage of dialysate, with a larger rise in BP observed during instillation. These changes were driven by changes in peripheral resistance that fell during drainage and rose during instillation. CONCLUSIONS: In contrast to hemodialysis, the acute effects of PD do not result in subclinical myocardial ischemia.
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Selby et al. (2010) conducted an observational in End-stage renal disease on peritoneal dialysis (n=10). Peritoneal dialysis exchange vs. Pre-exchange baseline was evaluated on Development of left ventricular regional wall motion abnormalities (RWMAs). A peritoneal dialysis exchange induced a very low frequency of regional wall motion abnormalities (5/100 regions), indicating it does not result in acute subclinical myocardial ischemia.
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