Follow Us:

social twitter box white 32 social facebook box blue 32social linkedin box blue 32 Youtube

Friday, 12 July 2019 15:38

ISN-ACT Global Trials Focus: CKD, dialysis and hypertension Featured

By  ISN Advancing Clinical Trials
Rate this item
(1 Vote)

This month, the first series of clinical trials curated by the ISN-Advancing Clinical Trials (ISN-ACT) team will get us thinking about nephrology research and encourage more discussion about chronic kidney disease, dialysis and hypertension: from PD catheter exit site care, the effectiveness of Roxadustat, to the initial treatment of hypertension in Sub-Saharan Africans and the role of CKD nurses in primary care.

The ISN-ACT team has collected some of the latest randomized research from nephrologists worldwide. Here, we focus on dialysis, hypertension and chronic kidney disease.

Join the debate @ISNeducation. Let us know if these trials will affect your practice? Are the results valid? How could the trials have been improved? What further studies are needed? If you would like to suggest any trials for inclusion in future editions, please send suggestions to research@theisn.org.

Read the main key points and outcomes of the following clinical trials. A list of all the ISN-ACT trial lists is also available on the ISN Academy, HERE.

Polyhexanide: an alternative to iodine for PD catheter exit site care

Topical antibiotic and antiseptic agents have been documented to reduce exit-site infection (ESI) and peritonitis in PD. The aim of this randomized controlled study was to evaluate the efficacy of polyhexanide in the prevention of ESI and peritonitis.

Effect of Local Polyhexanide Application in Preventing Exit-Site Infection and Peritonitis: A Randomized Controlled Trial. Ceri, et al. Ther Apher Dial. 2019 May 8. doi: 10.1111/1744-9987.12836.1283

Key points

  • Population: 93 peritoneal dialysis patients
  • Intervention vs Comparator: Regular exit-site application of polyhexanide vs. povidone-iodine
  • Time: 12 months.

Outcome

ESIs were similar, with 3 ESIs in the polyhexanide group and 5 ESIs in the povidone-iodine group (0.06 episodes/patient-year vs. 0.12 episodes/patient-year; P=NS).

Peritonitis rates were also similar, with 12 episodes with polyhexanide and 13 with povidone-iodine (0.26 episodes/patient-year vs. 0.32 episodes/patient-year, P=NS).

Polyhexanide appeared similarly effective to povidone-iodine for infection prophylaxis in patients on PD. However, the small size and methodological limitations of this study mean these findings should be interpreted with caution.

Roxadustat may be effectively dosed three times per week or weekly

This study evaluated the efficacy and safety/tolerability of Roxadustat, an oral hypoxia-inducible factor prolyl hydroxylase inhibitor, in Japanese anemic non-dialysis-dependent chronic kidney disease (NDD-CKD) patients.

Roxadustat Treatment of Chronic Kidney Disease-Associated Anemia in Japanese Patients Not on Dialysis: A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial. Akizawa, et al. Adv Ther. 2019;36(6):1438-1454Akizawa, et al. Adv Ther. 2019;36(6):1438-1454

Key points

  • Population: 107 patients with non-dialysis dependent CKD and anemia
  • Intervention vs Comparator: Roxadustat (thrice-weekly, variable dosing) vs. placebo
  • Time: 24 weeks.

Outcome

The response rate (Hb > 100g/L or >10g/L above baseline) was 94% in the Roxadustat group vs. 15% in the placebo group (P<0.001).

A subgroup of 56 participants who achieved Hb>110g/L on Roxadustat were re-randomized to continue thrice-weekly dosing or to reduce to once-weekly dosing. Both approaches resulted in a mean Hb > 10g/L at week 24.

In addition to providing further evidence of the efficacy of Roxadustat, this study suggests that less frequent dosing is feasible, although the long-term safety of this approach is not yet known.

CKD practice nurse and regular medical record audit does not affect progression of CKD in primary care

This cluster randomized trial aims to assess the effect of a nurse-led and primary care-based CKD management program to improve the outcomes of patients with CKD.

The Primary-Secondary Care Partnership to Improve Outcomes in Chronic Kidney Disease (PSP-CKD) Study: A Cluster Randomized Trial in Primary Care

Key points

  • Population: 46 primary care practices
  • Intervention vs Comparator: CKD nurse-specialist support to review and improve CKD care plus biannual medial record audit of renal function, blood pressure and related parameters vs. unsupported provision of biannual audit data
  • Time: 42 months.

Outcome

There was no difference in change in eGFR. However, coding accuracy improved and, at most timepoints, patients in the intervention practices were more likely to achieve blood pressure targets.

Nurse-supported CKD management in primary care did not protect renal function, but improvements in some aspects of care were noted.

Perindopril-amlodipine equal to perindopril-indapamide in pilot BP lowering study in Sub-Saharan diabetics

This trial investigated the short-term effects of two combination therapies on blood pressure control in sub-Saharan African type 2 diabetic individuals.

Short-term effects of perindopril-amlodipine vs perindopril-indapamide on blood pressure control in sub-Saharan type 2 diabetic individuals newly diagnosed for hypertension: A double-blinded randomised controlled trial. Sobngwi, et al. J Clin Hypertens (Greenwich). 2019 Jun 8. doi: 10.1111/jch.13557

Key points

  • Population: 30 type 2 diabetic participants with Grade I-II hypertension (treatment naïve)
  • Intervention vs Comparator: Perindopril 5mg-amlodipine 5mg vs. perindopril 5mg-indapamide 1.25mg
  • Time: 6 weeks.

Outcome

There was no difference in blood pressure (BP) lowering between two arms (24-hour systolic BP 144mmHg to 128mmHg [P=0.003] with perindopril/amlodipine vs. 145mmHg to 126mmHg with perindopril/indapamide [P=0.003]).

There were also no significant adverse events.

This pilot study suggests perindopril-amlodipine and perindopril-indapamide are equally efficacious in a sub-Saharan population. Although of insufficient size and duration to adequately assess adverse effects, this study may aid in the design of future trials in this population.

About the ISN-ACT monthly clinical trial list

The ISN-ACT sets out to leverage existing infrastructures within ISN, in order to improve global nephrology community participation in clinical trial research, through a series of activities and initiatives.

Read 1443 times Last modified on Monday, 15 July 2019 16:01

Global Operations Center

Avenue des Arts 1-2
1210 Brussels, Belgium
Tel: +32 2 808 04 20
Fax: +32 2 808 4454
Email contact

               

Americas Operations Center

340 North Avenue 3rd Floor
Cranford, NJ 07016-2496, United States
Tel: +1 567 248 9703
Fax: +1 908 272 7101
Email contact