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Dialysis Quality Improvement Needs Dialysis Registry: A Follow-up Study of Incident Hemodialysis Patients
Address for correspondence: Dr. Asheesh Kumar, Department of Nephrology, All India Institute of Medical Sciences Vijaypur, Jammu, India. E-mail: asheesh03.kapil@gmail.com
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Received: ,
Accepted: ,
This article was originally published by Wolters Kluwer - Medknow and was migrated to Scientific Scholar after the change of Publisher.
Dear Editor,
In India, kidney replacement therapy (RRT) is largely limited to urban areas.[1] An Indian study stated that definitive RRT was instituted in 34% of eligible patients.[2] Hemodialysis (HD) is the most common RRT modality. A dialysis registry is needed to monitor patients on HD.[3] As data on incident hemodialysis is scarce, we conducted this prospective observational study from November 2020 to December 2021. Adult patients having chronic kidney disease stage 5 (CKD-5) who presented with uremic symptoms and who were initiated on HD for the first time were included. All patients and their caregivers were counseled for regular HD and early arteriovenous fistula (AVF) creation till renal transplantation. After shared decision-making, a tunneled cuffed catheter was inserted for those ready for regular HD. Patients or attendants were contacted by phone at three monthly intervals. The concerned information included their well-being, current vascular access, and AVF creation status. There were 193 patients with a mean age of 61.5 ± 13.4 years [Table 1]. The follow-up time was 6–16 months. Twenty-four (12.4%) patients were lost to follow-up and 46 (23.8%) patients expired within 3 months. Among 123 (63.7%) patients who continued on hemodialysis after three months, the mortality was 47.2%. In India, these patients are not monitored because of the lack of a national registry for hemodialysis patients. In our study, the HD-dependent population was younger (75% being <64 years of age, which is higher than that stated in the ERS registry [~50%]) and had higher mortality (47.2%) at one year compared to other registries (50%) in four years.[4] With the implementation of the national dialysis program, the financial burden has decreased. Still, many factors need to be addressed for giving quality dialysis services. A government-supported centralized registry of dialysis patients and user-operated mobile apps can be possible solutions. Providing training, motivation, and incentives to the staff involved in dialysis for maintenance of records are other possible solutions for the same. A small sample size, limited follow-up, and patients being dialyzed at different dialysis centers in follow-up were the limitations. In conclusion, this study may pave large prospective studies to monitor and maintain quality dialysis services.
Variables | n=193 |
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Age (years), mean±SD | 61.5±13.4 |
18–20 years, n (%) | 2 (1.0) |
20–44 years, n (%) | 48 (24.9) |
45–64 years, n (%) | 98 (50.8) |
>65 years, n (%) | 45 (23.3) |
Sex (male-to-female ratio) | 1.7:1 |
Comorbidities | |
Hypertension, n (%) | 125 (64.7) |
Diabetes, n (%) | 65 (33.7) |
Hemoglobin (g%), mean+SD | 7.9±1.1 |
Follow-up duration (range) | 6-16 months |
Patients having follow-up and dialysis >90 days, n | 123 |
Dialysis duration (months), median (IQR) | 12 (6, 13) |
Continued on maintenance dialysis, n (%) | 65 (52.8) |
AVF created, n (%) | 39 (60) |
Death, n (%) | 58 (47.2) |
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
References
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