Cardiac Remodelling in Patients Undergoing in-Centre Nocturnal Haemodialysis: Results from the MIDNIGHT Study, a
Matthew P M Graham-Brown1, Darren R Churchward, Katherine L Hull
1National Centre for Sport and Exercise Medicine, Loughborough, UK.
Insights
Extended-hours haemodialysis (HD) offers significant cardiovascular benefits. In-centre nocturnal haemodialysis (INHD) improved left ventricular remodelling and reduced myocardial fibrosis compared to conventional HD.
Area of Science:
- Nephrology
- Cardiology
- Medical Imaging
Background:
- Extended-hours haemodialysis (HD) may enhance patient outcomes.
- In-centre nocturnal haemodialysis (INHD) is an underutilized HD method.
- Cardiovascular health is a key concern for HD patients.
Purpose of the Study:
- To assess the impact of INHD on left ventricular (LV) structure, function, and myocardial fibrosis.
- To compare INHD with conventional HD regarding cardiovascular and clinical markers.
- To evaluate changes in quality-of-life and clinical measures.
Main Methods:
- A 6-month, non-randomized controlled trial comparing 13 INHD patients with 12 conventional HD controls.
- Cardiac magnetic resonance imaging and native T1 mapping were used to assess LV remodelling and fibrosis.
- Quality-of-life questionnaires and clinical parameters were collected.
Main Results:
- INHD significantly reduced LV mass (p=0.02) and global T1 values (p=0.05) compared to controls.
- Significant reductions in non-septal native T1 values (p=0.02) indicated decreased myocardial fibrosis with INHD.
- INHD also improved serum phosphate levels (p=0.03) and reduced ultrafiltration rates (p=0.05).
Conclusions:
- Six months of INHD promotes favorable left ventricular remodelling.
- INHD is associated with reduced myocardial fibrosis compared to conventional HD.
- INHD shows potential for improving cardiovascular health in dialysis patients.
Abstract:
Evidence suggests extended-hours haemodialysis (HD) may improve cardiovascular, medical and quality-of-life outcomes. In-centre nocturnal haemodialysis (INHD) is an established but underutilized method of providing extended-hours treatment. This 6-month, non-randomized controlled trial (ISRCTN16672784) recruited 13 INHD patients and 12 control patients on conventional HD. The effects of treatment on left ventricular (LV) structure, function and myocardial fibrosis were assessed using cardiac magnetic resonance imaging and native T1 mapping. Quality-of-life and clinical measures were also collected. INHD led to significant reductions in LV mass (-14.75 vs. +6.54 g; p = 0.02), global T1 (-30.62 vs. 0.4 ms; p = 0.05) and non-septal native T1 values (-30.93 vs. 8.96 ms; p = 0.02) over time. There were also significant improvements in serum phosphate (-0.39 vs. +0.02 mmol/L; p = 0.03) and reductions in ultrafiltration rates (-2.32 vs. +0.70 mL/h/kg p = 0.05) between INHD and controls. Six-months of INHD was associated with favourable LV remodelling and reduced myocardial fibrosis compared to patients on conventional haemodialysis.
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