Abstract
Introduction
With increased fluid intake and tolvaptan treatment, the growth rate of cysts can be theoretically decelerated in autosomal polycystic kidney disease. In this prospective study, it was planned to evaluate thirst sensation in these patients and the parameters affecting its intensity.
Methods
Forty-one ADPKD patients on tolvaptan and 40 ADPKD patients not on tolvaptan as the control group were evaluated for thirst distress sensation and intensity. The feeling of thirst and the discomfort caused by excessive fluid intake was assessed with Thirst Distress Scale-HF 12 questions (60/12). Thirst intensity was evaluated with a 100 mm visual scale.
Results
Of the whole group, 35.8% (29) were males, and 64.2% (52) were females. The mean age of the tolvaptan group was 39.17 ± 9.35 years and for the control group, it was 41.95 ± 12.29 years. There was a negative correlation between the thirst distress score of the patients and an increase in creatinine level after a year of tolvaptan treatment (r = − 0.335, p = 0.035). The patients not taking thiazide had higher thirst intensity scores (p = 0.004). There was no impact of tolvaptan dosage, total kidney volume, serum sodium, urinary osmolarity or eGFR on thirst distress and thirst intensity scores.
Discussion/conclusion
Only thiazide co-treatment had a positive impact on thirst distress and intensity when given tolvaptan. Thirst Distress Scale for ADPKD patients can be used to classify patients before and during tolvaptan treatment.
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Data availability
All data generated and analyzed during this study were included in this article. Further enquiries can be directed to the corresponding author.
Change history
10 July 2023
A Correction to this paper has been published: https://doi.org/10.1007/s10157-023-02375-5
References
Bergmann C, Guay-Woodford LM, Harris PC, et al. Polycystic kidney disease. Nat Rev Dis Primers. 2018. https://doi.org/10.1038/S41572-018-0047-Y.
Torres VE, Chapman AB, Devuyst O, et al. Tolvaptan in patients with autosomal dominant polycystic kidney disease. N Engl J Med. 2012;367:2407–18.
Torres VE, Chapman AB, Devuyst O, et al. Tolvaptan in later-stage autosomal dominant polycystic kidney disease. N Engl J Med. 2017;377:1930–72.
Müller RU, Messchendorp AL, Birn H, et al. An update on the use of tolvaptan for autosomal dominant polycystic kidney disease: consensus statement on behalf of the ERA working group on inherited kidney disorders, the European rare kidney disease reference network and polycystic kidney disease international. Nephrol Dial Transplant. 2022;37:825–39.
Torres VE. Pro: Tolvaptan delays the progression of autosomal dominant polycystic kidney disease. Nephrol Dial Transplant. 2019;34:30–4.
Torres VE, Higashihara E, Devuyst O, et al. Effect of tolvaptan in autosomal dominant polycystic kidney disease by CKD stage: results from the TEMPO 3:4 trial. Clin J Am Soc Nephrol. 2016;11:803–11.
Edwards ME, Chebib FT, Irazabal M, et al. Long-term administration of tolvaptan in autosomal dominant polycystic kidney disease. Clin J Am Soc Nephrol. 2018;13:1153–61.
Physiology of thirst and drinking: implication for nursing practice-PubMed.
Oberdhan D, Cole JC, Krasa HB, et al. Development of the autosomal dominant polycystic kidney disease impact scale: a new health-related quality-of-life instrument. Am J Kidney Dis. 2018;71:225–35.
Nutr A, Bichet DG. Vasopressin and the regulation of thirst. Ann Nutr Metab. 2018;72:3–7.
Waldréus N, Jaarsma T, van der Wal MHL, et al. Development and psychometric evaluation of the thirst distress scale for patients with heart failure. Eur J Cardiovasc Nurs. 2018;17:226–34.
WHODAS 2.0 Translation package whodas 2.0 translation package (version 1.0) translation and linguistic evaluation protocol and supporting material i. Preface.
Higashihara E, Nutahara K, Tanbo M, et al. Does increased water intake prevent disease progression in autosomal dominant polycystic kidney disease? Nephrol Dial Transplant. 2014;29:1710–9.
Katsumata M, Hirawa N, Sumida K, et al. Effects of tolvaptan in patients with chronic kidney disease and chronic heart failure. Clin Exp Nephrol. 2017;21:858–65.
Irazabal MV, Torres VE, Hogan MC, et al. Short-term effects of tolvaptan on renal function and volume in patients with autosomal dominant polycystic kidney disease. Kidney Int. 2011;80:295–301.
Eng SH, Waldréus N, González B, et al. Thirst distress in outpatients with heart failure in a Mediterranean zone of Spain. ESC Heart Fail. 2021;8:2492.
Porcu M, Fanton E, Zampieron A. Thirst distress and interdialytic weight gain: a study on a sample of haemodialysis patients. J Ren Care. 2007;33:179–81.
Kara B. Determinants of thirst distress in patients on hemodialysis. Int Urol Nephrol. 2016;48:1525–32.
Niu J-Y, Fan W-F, Zhang Q, et al. Study on the clinical significance and related factors of thirst and xerostomia in maintenance hemodialysis patients. Kidney Blood Press Res. 2013;37:464–74.
Altun İ, Çınar ND, Kaşıkçı MK. Self-reported quantity of daily water intake and urine output in healthy young. Int J Urol Nurs. 2012;6(2):91–3. https://doi.org/10.1111/j.1749-771X.2012.01143.x.
Thapa K, Das S, Pathak P, et al. Assessment of thirst intensity and thirst distress and the practices for its management among heart failure patients admitted to the cardiology unit. J Pract Cardiovas Sci. 2021;7:36.
Waldréus N, Chung ML, van der Wal MHL, et al. Trajectory of thirst intensity and distress from admission to 4-weeks follow up at home in patients with heart failure. Pat Prefer Adher. 2018;12:2223–31.
Hughes F, Mythen M, Montgomery H. The sensitivity of the human thirst response to changes in plasma osmolality: a systematic review. Periop Med. 2018. https://doi.org/10.1186/S13741-017-0081-4.
Rangan GK, Wong ATY, Munt A, et al. Prescribed water intake in autosomal dominant polycystic kidney disease. NEJM Evidence. 2021. https://doi.org/10.1056/EVIDOA2100021.
Torres VE. Vasopressin antagonists in polycystic kidney disease. Semin Nephrol. 2008;28:306.
Gabow PA, Kaehny WD, Johnson AM, et al. The clinical utility of renal concentrating capacity in polycystic kidney disease. Kidney Int. 1989;35:675–80.
Uchiyama K, Kitayama C, Yanai A, et al. The effect of trichlormethiazide in autosomal dominant polycystic kidney disease patients receiving tolvaptan: a randomized crossover controlled trial. Sci Rep. 2021;11:17666.
Kramers BJ, van Gastel MDA, Meijer E, et al. Case report: a thiazide diuretic to treat polyuria induced by tolvaptan. BMC Nephrol. 2018;19:1–5.
van Gastel MDA, Torres VE. Polycystic kidney disease and the vasopressin pathway. Ann Nutr Metab. 2017;70:43–50.
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Conception: SB, NW. Design: SB, NW. Supervision: SB. Data collection: NY, ME, MT, MI, IS, DGT, NE, BK, ED. Analysis and interpretation: Sibel Bek, Sibel Balcı. Literature review: Sibel Bek, Mahmut Islam, Nana Waldreus. Writer: Sibel Bek, Mahmud Islam.
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The study complies with the Declaration of Helsinki. Ethics approval for the study was obtained from the Ethics Committee of Kocaeli University Hospital (GOKAEK-2021/12.03). Written informed consent was obtained from the participants who volunteered to take the survey and participate in the study.
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The original online version of this article was revised: In the original publication, the corresponding author name has been inadvertently appeared as Sibel Gokcay Gokcay Bek.
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Gocay Bek, S.G., Yıldız, N., Islam, M. et al. Thirst intensity survey in ADPKD patients. Clin Exp Nephrol 27, 819–827 (2023). https://doi.org/10.1007/s10157-023-02373-7
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DOI: https://doi.org/10.1007/s10157-023-02373-7