| Home | E-Submission | Sitemap | Contact Us |  
Child Kidney Dis > Volume 22(2); 2018 > Article
Hwang, Kim, Kim, and Lee: Primary Polydipsia in Children: Two Case Reports


Primary polydipsia (PP) is marked by an increase in thirst, and most often presents in patients with psychiatric illnesses. Although uncommon in children, we experienced cases of PP in a 15-month-old boy and a 5-year-old girl. Both were admitted to the hospital with symptoms of polydipsia and polyuria that appeared 1–3 months before admission. Brain magnetic resonance imaging in both patients was normal. A water restriction test was performed after hospitalization and showed normal results. The symptoms improved after the parents were instructed to implement water-intake restriction for 2 weeks. Our report provides useful information for the treatment of PP in children.


Primary polydipsia (PP) is a clinical disorder characterized by excessive thirst leading to excessive fluid intake and consequential excessive excretion of urine without an obvious cause [1]. Polydipsia is defined as the consumption of water higher than 2 L/m2/24 h in children and characterized by a urine volume in excess of 2 L/m2/24 h or 150 mL/kg/24 h at birth, 100–110 mL/kg/24 h until the age of 2 years, and 40–50 mL/kg/24 h in older children and adults [2,3]. PP is commonly observed in patients with psychiatric problems such as schizophrenia, it is also known as psychogenic polydipsia [1].
Differential diagnosis based on the symptoms of polydipsia and polyuria is difficult because of the broad associated disease spectrum, including renal, endocrine, and neurological diseases [4]. For example, differentiating PP from diabetes insipidus (DI) can be difficult, and the diagnostic gold standard to understand this difference is a water restriction test. Water restriction tests for older infants and children should be performed in the hospital under close medical supervision. The patient should not be allowed to lose more than 5% of body weight. Monitoring of vital signs (temperature, pulse, and blood pressure), body weight, laboratory tests, urine and plasma osmolarities, and plasma sodium concentration are essential. Each urine void should be recorded and urine volume, specific gravity, and osmolality should be measured. While polyuria in true DI occurs because of defective secretion or response to the antidiuretic hormone (ADH), in PP, there is a disturbance in thirst control that is not related to impaired ADH production or release.
Here, we report the cases of a 15-month-old boy and a 5-year-old girl who presented with symptoms of PP. As there are few reports on the progression of polydipsia and polyuria in children with PP, the present report will inform the provision of care to PP patients.

Case report

1. Case 1

A 15-month-old boy presented to our clinic with symptoms of polydipsia (150 mL/kg) and polyuria that appeared 1 month prior to his visit. His consumption of water increased such that he woke up 3–4 times nightly to drink water. His thirst was unquenchable. Based on his history, it was apparent that he was born by cesarean section with a birth weight of 3,880 g [50–75 percentile (p)] at 40 weeks and 3 days of gestation age. When he visited our clinic, upon physical examination, his general status was good. His blood pressure was 100/60 mmHg, respiratory rate was 40 breaths/min, and body temperature was 37℃. His body weight was 13 kg (90–95 p), and his height was 77 cm (10–25 p). Upon neurological examination, his muscle tonus and deep tendon reflexes were normal. Other physical examination findings were nonspecific. His laboratory tests were as follows: white blood cell (WBC) count 15,230/μL, hemoglobin 13.1 g/dL, platelets 348,000/mm3, sodium 137 mEq/L, potassium 4.8 mEq/L, chloride 109 mEq/L, blood urea nitrogen (BUN) 9 mg/dL, creatinine 0.24 mg/dL, albumin 4.6 g/dL, hemoglobin A1c 5.1%, insulin 3.8 uIU/mL, and C-peptide 1.38 ng/mL. Cortisol level was normal, urine osmolarity was 196 mOsm/kg, and serum osmolarity was 284 mOsm/kg. The spot urine test showed a sodium level 20 mmol/L, potassium level 17.2 mmol/L, and creatinine level 22 mgl/dl. The fractional excretion of sodium was 0.2%. A water restriction test was performed after admission and the test result showed that serum osmolarity was unchanged at 277–287 mOsm/kg, while urine osmolarity was elevated at 737 mOsm/kg (Table 1). The ADH level was 6.25 pg/mL at the beginning of the test and 12 pg/mL at the end of the test. Urine output was 551 mL/day. The brain sellar MRI and kidney ultrasonography results were normal. At admission, he was instructed to alter his water-drinking behavior and was provided with psychiatric support. His parents did not allow the child to drink water before sleep and allowed him to play with toys instead of drinking water. Two weeks later, he was followed up at an outpatient clinic. His body weight was 14.3 kg and daily water intake was 70 mL/kg. Four weeks later, his body weight was 14.2 kg, daily water intake was 35–50 mL/kg, and daily urine output was 40–45 mL/kg.

2. Case 2

A 5-year-old girl presented to our clinic with complaints of 180 mL/kg polydipsia and 150 mL/kg polyuria that appeared 3 months prior to her visit. At that time of the visit, her water intake had increased further, and she had started to wake up 3–4 times every night to drink water. She was born by vaginal delivery and had a birth weight of 3,300 g (50–75 p) at 40 weeks of gestation age. When she visited our clinic, upon physical examination, her general status was satisfactory. Her blood pressure was 95/60 mmHg, respiratory rate was 24 breaths/min, and body temperature was 36.4℃. Her body weight was 22.6 kg (90–95 p), and her height was 114 cm (70–95 p). Upon neurological examination, her muscle tonus and deep tendon reflexes were normal, as were other physical examination findings. Her laboratory tests were as follows: WBC count 7,610/μL, hemoglobin 13.6 g/dL, platelets 351,000/mm3, sodium 136 mEq/L, potassium 4.4 mEq/L, chloride 101 mEq/L, BUN 13 mg/dL, creatinine 0.32 mg/dL, albumin 4.9 g/dL, and HbA1C 5.4%. Cortisol levels were normal. Urine osmolarity was 226 mOsm/kg, and serum osmolarity was 280 mOsm/kg. The spot urine test showed a sodium level 11 mmol/L, potassium level 45.8 mmol/L, and creatinine level 21.88 mg/dL. The fraction excretion of sodium was 0.1%. A water restriction test was performed after admission, and her serum osmolarity was consequently unchanged at 283–288 mOsm/kg, while her urine osmolarity was elevated at 1,008 mOsm/kg (Table 2). The ADH level was 5.38 pg/mL at the beginning of the test and 8.06 pg/mL at the end of the test. The brain sellar MRI and kidney ultrasonography results were normal. She altered her water-drinking behavior and was provided with psychiatric support. Her parents were instructed to not allow her to drink water before sleep and daily water intake was limited to 1 L. If she wanted to drink water, it would not be provided immediately, and she would be offered her favorite doll to play with instead. If the interest in water was reduced through play, the amount of water intake could be correspondingly decreased. Two weeks later, follow-up was performed at an outpatient clinic. Her body weight was 23 kg, daily water intake was 40 mL/kg, and daily urine output was 40–45 mL/kg.


PP is a specific disorder related to thirst that rarely occurs in childhood. Most PP cases described in the literature concern adults who also have severe psychiatric comorbidities [5]. In patients with PP, symptoms generally develop in three phases. They begin with polydipsia and polyuria, followed by hyponatremia (water is retained as the kidneys fail to excrete excess fluid, resulting in low sodium serum values), and finally water intoxication [6]. Acute hyponatremia develops when excessive fluid consumption leads to a rapid fall of serum sodium. An acute drop in serum sodium level of 10 mEq/L over a few hours may produce recognizable clinical symptoms, including diarrhea, salivation, nausea, ataxia, stupor, and coma. The above three stages did not appear in our patients because the symptoms had recently begun, the kidneys were functioning normally, and the serum sodium levels were normal. In the cases described here, urine concentration normalized when water intake was restricted. PP is most often associated with behavioral dysregulation of water intake in infancy or early childhood. In children without laboratory signs of diabetes, PP is most often confused with DI. PP can cause physiological suppression of serum ADH, which results in increased output of hypo-osmolar urine [2]. The primary means of distinguishing between DI and PP is the water deprivation test, which is more sensitive than an exogenous ADH challenge.
Consequently, PP is more often confused with central DI than with nephrogenic DI. Several clinical and laboratory findings can aid in the differentiation between these two conditions. In addition, in cases of PP caused by psychogenic factors, drinking water is compulsive; therefore, when water intake is restricted, urine becomes concentrated. Cases of psychogenic PP can be identified by measuring vasopressin concentrations in the absence of any underlying disease if differentiation based on water restriction is insufficient.
Grunberg et al [7]. reported one patient who began to consume excessive water at 20 months of age and was diagnosed with PP at 3 years of age. The authors reported that their patient with PP had recovered 2 months later with the help of water restriction only and without any other treatment. Moreover, that patient underwent a water restriction test for the differentiation between DI and PP [8]. Diagnosis in children with PP is challenging because of difficulties with the water restriction test. The water restriction test is intended to restrict the infant’s need to drink water and to monitor urine and blood osmotic concentrations every hours for any changes. It is generally difficult to perform this on an outpatient basis. A urinary osmolarity greater than 600 mOsm/kg during the water restriction test is sufficient for a diagnosis of PP [9]. We described here two patients with PP who were diagnosed via a water restriction test. Additionally, we reported in these cases the progress of polydipsia and its recovery without any pharmacological treatment. The treatment of PP aims to alter the patient’s drinking behavior, and fluid restriction and psychiatric support are sufficient for treatment in most cases [10]. Restriction of up to 50% to 60% of daily fluid requirements may be required to achieve the goal of inducing a negative water balance [8] .
Our patients were found to have no additional underlying disease based on the water restriction test, brain MRI, or ADH level test. Their symptoms improved within 1 month of observation without any pharmacological treatment. Few studies have reported progress in the treatment of PP patients with water restriction. Our findings suggest that PP treatment in children requires at least 2 weeks of consistent habitual correction via water restriction. The present report provides useful information for the treatment of pediatric PP cases. Notably, our findings suggest that PP treatment in children requires at least two weeks of habitual correction via water restriction.


This paper was supported by funds from the Biomedical Research Institute, Chonbuk National University Hospital.


Patient consent
This study was approved by the institutional review board (CUH 2018-05-041), and the requirement for informed consent was waived due to the retrospective nature of the study.


Conflict of interest
No potential conflict of interest relevant to this article was reported.


1. Tournikioti K, Voumvourakis K, Moussas G, Plachouras D, Michopoulos I, Douzenis A, et al. Primary polydipsia: A case report. J Nerv Ment Dis. 2013;201: 709-1.
crossref pmid
2. van Santen HM, Jöbsis JJ, Kamp G. A practical algorithm for polydipsia in children. Ned Tijdschr Geneeskd. 2014;158: A7595.
3. Di Iorgi N, Napoli F, Elsa Maria Allegri A, Olivieri I, Bertelli E, Gallizia A, et al. Diabetes insipidus – Diagnosis and management. Horm Res Paediatr. 2012;77: 69-84.
crossref pmid
4. Metropulos D, Antoon JW. Primary polydipsia in a child. Clin Pediatr (Phila). 2015;54: 1396-8.
crossref pmid
5. Cronin RE. Psychogenic polydipsia with hyponatremia: Report of eleven cases. Am J Kidney Dis. 1987;9: 410-6.
crossref pmid
6. Şahin ve ark. A case of primary polydipsia presenting with severe malnutrition. Turk Arch Ped. 2013;251-4.

7. Grunberg J, Gazzara G, Lopez P, Esquivel N. Psychogenic polydipsia in a child. Bol Med Hosp Infant Mex. 1981;38: 807-15.
8. Tarım O. Disorders of water homeostasis in children. Turkiye Klinikleri J Pediatr Sci. 2006;2: 108-14.

9. Robertson GL. Diabetes insipidus: differential diagnosis and management. Best Pract Res Clin Endocrinol Metab. 2016;30: 205-18.
crossref pmid
10. Ergin H, Semiz S, Dağdeviren E. Psychogenic polydipsia: A case report. Cocuk sağlığı ve Hastalıkları Dergisi. 2006;49: 319-21.

Table 1.
Water Restriction Test in a 15-month-old Boy
Time (h) 1 2 3 4 5 6
Body weight (kg) 13.5 13.2 13.1 13 13 13.1
Serum Na (mmol/L) 137 137 137 139 139 139
Serum osmolarity (mOsm/kg) 284 281 287 277 285 287
Urine specific gravity 1.006 1.016 1.023
Urine osmolarity (mOsm/kg) 196 327 492 - 737 603
ADH (pg/mL) 6.25 12.02
Urine output 1.8 cc/kg/day
Table 2.
Water Restriction Test in a 5-year-old Girl
Time (h) 1 2 3 4 5 6
Body weight (kg) 22.6 22.9 22.6 22.6 22.3 22.3
Serum Na (mmol/L) 137 136 136 136 137 139
Serum osmolarity (mOsm/kg) 283 281 281 283 288 285
Urine specific gravity 1.007 1.016 1.031
Urine osmolarity (mOsm/kg) 226 325 523 954 1008 921
ADH (pg/mL) 4.28 13.15
Urine output 1.3 cc/kg/day
Editorial Office
Room 103, 124, Bukbyeonjung-ro, Gimpo-si, Gyeonggi-do 10098, Republic of Korea
TEL : +82-31-987-5963   FAX : +82-31-987-5967   E-mail : ckdeditor@kspn.org

Copyright© Korean Society of Pediatric Nephrology. All rights reserved.                powerd by m2community
About |  Browse Articles |  Current Issue |  For Authors and Reviewers