Abstract: TH-PO242
Symptom Burden with Calcium Carbonate Compared to Sevelamer in Haemodialysis Patients
Session Information
- Hemodialysis and Frequent Dialysis - II
November 07, 2019 | Location: Exhibit Hall, Walter E. Washington Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: Dialysis
- 701 Dialysis: Hemodialysis and Frequent Dialysis
Authors
- Pan, Fei Fei Mary, The Royal Melbourne Hospital, Parkville, Victoria, Australia
- Toussaint, Nigel David, The Royal Melbourne Hospital, Parkville, Victoria, Australia
- Moodie, Jo-anne M., The Royal Melbourne Hospital, Parkville, Victoria, Australia
- Isac, Tessy, Melbourne health, Melbourne, New South Wales, Australia
- Smith, Edward R., The Royal Melbourne Hospital, Parkville, Victoria, Australia
- Champion de Crespigny, Paul J., The Royal Melbourne Hospital, Parkville, Victoria, Australia
- Hewitson, Timothy D., The Royal Melbourne Hospital, Parkville, Victoria, Australia
- Holt, Stephen G., The Royal Melbourne Hospital, Parkville, Victoria, Australia
Background
Patients with CKD frequently experience a considerable symptom burden which interferes with quality of life. Gastrointestinal tract (GIT) symptoms, including nausea, vomiting, constipation and diarrhoea, affect 10-40% of CKD patients. Medications, including phosphate binders (PB), often contribute to this symptom burden. We compared symptoms on the calcium-based phosphate binder, calcium carbonate (CC) therapy with those on sevelamer in a clinical trial.
Methods
Prevalent haemodialysis (HD) patients were recruited into a randomised study (n=37). Total study duration was 37 weeks, including 1 week of PB ‘washout’. Participants were randomised to either i) 36 weeks of CC therapy or ii) 12 weeks of CC, followed by 24 weeks of sevelamer therapy. Patient symptoms were assessed with the Palliative Care Outcome Scale-Renal Version (POS) and analysed according to total scores and individual scores for specific GIT symptoms.
Results
26 participants completed the study, and were analysed according to intention-to-treat analysis. 10 participants were randomised to the CC only arm, whilst 16 to the CC/sevelamer arm. There were no statistically significant differences in baseline demographics or co-morbidities between the groups. At baseline, median total POS scores were 10 (interquartile range: [IQR] 7-14) in the CC only arm vs. 13 (IQR 3-19) in the CC/sevelamer arm. At study completion, median POS scores were 12 (IQR 7-13) in the CC only arm, vs 8 (IQR 2-13) in the CC/sevelamer arm, with no statistically significant differences between groups at any timepoint. With regards to GIT symptoms, the proportion of patients experiencing improvement in nausea from baseline to study end were 30% and 44% in the CC only and CC/sevelamer arms respectively, and for vomiting, 10% vs 25% experienced improvement in the respective groups. 20% of CC only patients had more severe constipation at study end vs 31% in the CC/sevelamer group; and for diarrhoea, 30% of CC only vs 35% of CBPB/sevelamer patients reported increased symptoms. None of the changes in specific GIT symptoms were statistically significant.
Conclusion
Symptom burden of patients on HD did not change significantly with different PB therapy in our study, with similar changes in GIT symptoms over time comparing CC and sevelamer therapy.
Funding
- Commercial Support –