Author(s):
Rose Mary Joshy, Ragi Rajan, Binu Jose, Binu Upendran
Email(s):
jollyveliath74@gmail.com
DOI:
10.52711/2231-5691.2026.00037
Address:
Rose Mary Joshy1, Ragi Rajan1, Binu Jose1, Binu Upendran2
1Department of Pharmacy Practice, St. Joseph’s College of Pharmacy, Cherthala, Alappuzha, 688524, Kerala, India.
2MD, DNB (MED), DM DNB, Head of Department Nephrology, Lourdes Hospital, Ernakulam, 682012, Kerala, India.
*Corresponding Author
Published In:
Volume - 16,
Issue - 3,
Year - 2026
ABSTRACT:
Background: Chronic kidney disease is characterised as a sustained and progressive loss of renal function, commonly progressing to end-stage renal disease (ESRD), where maintenance hemodialysis becomes a necessity. But hemodialysis can precipitate or exacerbate electrolyte imbalances. These disturbances particularly in phosphorus, potassium, and calcium, are linked to pruritus, mineral bone disorders, and increased cardiovascular risk. Objective: To evaluate the biochemical parameters (electrolyte imbalances) and clinical profile (Pruritus, CKD MBD) among CKD stage V patients on maintenance hemodialysis, and to assess the correlation between biochemical markers and clinical outcomes. Methodology: A prospective observational study was conducted at Lourdes Hospital, Kerala, enrolling 91 adults with Chronic renal failure on hemodialysis. Biochemical parameters (serum potassium, calcium, phosphorus and calcium–phosphorus product) were measured at baseline and at three months. Clinical assessments included pruritus – assessed using the 12-PSS and indicators of mineral bone disorder, muscle weakness. Statistical analysis was performed via SPSS and correlation between variables estimated. Results: Electrolyte abnormalities were highly prevalent at baseline, with hyperphosphatemia (73.6%) and hyperkalemia (36.3%) most common. After three months of dialysis and individualized management, the overall proportion of patients with any electrolyte abnormality decreased but remained substantial to 61.5% and 17.6% respectively. Pruritus affected roughly one quarter of patients(24.2%) and showed a significant association with elevated serum phosphorus and higher calcium–phosphorus product. It was also observed that higher calcium phosphate product correlated with increased risk of developing CKD-MBD. Hypocalcaemia-related muscle cramps were also reported in 9.9%, indicating the neuromuscular effects of disrupted calcium balance. Conclusions: Electrolyte disturbances remain frequent in hemodialysis patients despite ongoing therapy, with hyperphosphatemia and hyperkalemia particularly prominent. Regular monitoring and tailored interventions are essential to reduce long-term complications.
Cite this article:
Rose Mary Joshy, Ragi Rajan, Binu Jose, Binu Upendran. A Study to Assess Electrolyte Imbalances and related Complication in Chronic Kidney Disease patients undergoing Hemodialysis. Asian Journal of Pharmaceutical Research. 2026; 16(3):251-6. doi: 10.52711/2231-5691.2026.00037
Cite(Electronic):
Rose Mary Joshy, Ragi Rajan, Binu Jose, Binu Upendran. A Study to Assess Electrolyte Imbalances and related Complication in Chronic Kidney Disease patients undergoing Hemodialysis. Asian Journal of Pharmaceutical Research. 2026; 16(3):251-6. doi: 10.52711/2231-5691.2026.00037 Available on: https://www.asianjpr.com/AbstractView.aspx?PID=2026-16-3-5
REFERENCE:
1. Kidney Disease: Improving Global Outcomes (KDIGO) CKD Work Group. KDIGO 2024 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Kidney Int. 2024; 105(4S): S117–S314 https:/kdigo.org/wp content/uploads/2024/03/KDIGO-2024-CKD-Guideline.pdf
2. Timofte D, Tanasescu MD, Balcangiu-Stroescu AE, Balan DG, Tulin A, Stiru O, et al. Dyselectrolytemia—management and implications in hemodialysis: A review. Exp Ther Med. 2021; 21(1): 102. doi:10.3892/etm.2020.9430.
3. Waziri B, Duarte R, Naicker S. Chronic kidney disease–mineral and bone disorder (CKD MBD): current perspectives. Int J Nephrol Renovasc Dis. 2019; 12: 263–276. doi:10.2147/IJNRD.S191156
4. Block GA, Klassen PS, Lazarus JM, Ofsthun N, Lowrie EG, Chertow GM. Mineral metabolism, mortality, and morbidity in maintenance hemodialysis. J Am Soc Nephrol. 2004 Aug; 15(8): 2208-18
5. Palmer SC, Hayen A, Macaskill P, Pellegrini F, Craig JC, Elder GJ, et al. Serum levels of phosphorus, parathyroid hormone, and calcium and risks of death and cardiovascular disease in individuals with chronic kidney disease: a systematic review and meta-analysis. JAMA. 2011 Mar 16; 305(11): 1119-27.
6. Hasan SM, Kumar HD, Prasher PK, Goel R. A study of complications encountered in patients undergoing hemodialysis procedure. Int J Adv Res. 2017; 5(11): 877-884. doi:10.21474/IJAR01/5843
7. Pisoni RL, Wikström B, Elder SJ, Akizawa T, Asano Y, Keen ML, et al. Pruritus in haemodialysis patients: international results from the Dialysis Outcomes and Practice Patterns Study (DOPPS). Nephrol Dial Transplant. 2006 Dec; 21(12): 3495-505.
8. Narita I, Iguchi S, Omori K, Gejyo F. Uremic pruritus in chronic hemodialysis patients. J Nephrol. 2008 Mar-Apr;21(2):161-5.
9. Mettang T, Kremer AE. Uremic pruritus. Kidney Int. 2015 Apr; 87(4): 685-91.
10. Tsuchiya K, Akihisa T. The importance of phosphate control in chronic kidney disease. Nutrients. 2021; 13(5): 1670. doi:10.3390/nu1305167039.
11. Goodman WG, Goldin J, Kuizon BD, Yoon C, Gales B, Sider D, et al. Coronary-artery calcification in young adults with end-stage renal disease who are undergoing dialysis. N Engl J Med. 2000 May 18; 342(20): 1478-83.
12. Guttee V, Nie Y, Wang Y, Ding X. Impact of abnormal serum electrolyte levels and acid-base disorders on clinical outcomes among maintenance hemodialysis patients. Open Access Libr J. 2017; 4: 1-13. doi:10.4236/oalib.1103623
13. Ketteler M, Block GA, Evenepoel P, Fukagawa M, Herzog CA, McCann L, et al. Executive summary of the 2017 KDIGO Chronic Kidney Disease–Mineral and Bone Disorder (CKD-MBD) Guideline Update: what’s changed and why it matters. Kidney Int. 2017 Jul; 92(1): 26-36.
14. Evenepoel P, Cunningham J, Ferrari S, Haarhaus M, Javaid MK, Lafage-Proust MH, et al. European Consensus Statement on the diagnosis and management of hyperphosphataemia in patients with chronic kidney disease. Nephrol Dial Transplant. 2016 Sep; 31(9): 1392-9.
15. Chertow GM, Levin NW, Beck GJ, Depner TA, Eggers PW, Gassman JJ, et al. In-Center Hemodialysis Six Times per Week versus Three Times per Week. N Engl J Med. 2010 Dec 9; 363(24): 2287-300
16. Reich A, Bożek A, Janiszewska K, Szepietowski JC. 12‑Item Pruritus Severity Scale: development and validation of new itch severity questionnaire. Biomed Res Int. 2017; 2017: 3896423. doi:10.1155/2017/3896423
17. Bover J, Ureña P, Aguilar A, Mazzaferro S, Benito S, López-Báez V, et al. Alkaline Phosphatases in the Complex Chronic Kidney Disease-Mineral and Bone Disorders. Calcif Tissue Int. 2018 Jul;103(1):111-124
18. Monisha M. Impact of dialysis on serum electrolytes in end stage renal disease. IOSR J Biotechnol Biochem.2018; 4(4): 49-53. doi:10.9790/264X-0404024953.
19. Rayner HC, Larkina M, Wang M, Graham-Brown M, van der Veer SN, Ecder T, et al. International Comparisons of Prevalence, Awareness, and Treatment of Pruritus in People on Hemodialysis. Clin J Am Soc Nephrol. 2017 Dec 7; 12(12): 2000-2007
20. Momose A , Kudo S, Sato M, Nagai H, Yasuo T. Calcium ions are abnormally distributed in skin of haemodialysis patients with uremic pruritus. Nephrol Dial Transplant. 2004; 19(8): 2061-66