ESPE Abstracts (2019) 92 P2-21

Fludrocortisone Treatment in a Child with Postural Orthostatic Tachycardia Syndrome (POTS): A Case Report

Gaia Varriale1, Marco Greco1, Luciano De Simone2, Anna Pozzessere3, Stefano Stagi1

1Health Sciences Department, University of Florence, Anna Meyer Children's University Hospital, Firenze, Italy. 2Paediatric Cardiology Anna Meyer Children Hospital, Firenze, Italy. 3Clinical Pediatric Department, Anna Meyer Children Hospital, Firenze, Italy

Background: Postural orthostatic tachycardia syndrome (POTS) is a multifactorial condition, which implies symptoms as fatigue, tachycardia, sleep disorders and autonomic symptoms. The fundamental clinical sign is the manifestation of an abnormal increase in heart rates of at least 40 bpm within 10 minutes assuming an upright position, delineating a condition of orthostatic intolerance and decreasing quality of life.

Objective: To describe a case of a debilitated boy with POTS treated with fludrocortisone, justifying our therapeutic choice based on syndrome's pathophysiology.

Case report: An 8-year-old boy presented repeated episodes of tachycardia, pallor, periumbilical abdominal pain and frontal headache, followed by ground fall and loss of consciousness lasting a few seconds. Therefore, he performed first-level blood tests, ECG, chest X-ray, abdominal ultrasound and fundus oculi, resulting normal. Moreover, due to the worsening of the symptoms, he performed an echocardiography and a recording Holter pressure, without finding anomalies.

At our attention, to rule out intracranial pathology, a brain MRI and electroencephalography were made, resulting without abnormalities. Finally, a head-up tilt table test was performed, showing a vasovagal response, so the therapy with midodrine hydrochloride at the dose of 2.5mg/die was started.

After the hospitalization, his symptomatology has become more frequent. So he was admitted for second times in our Hospital, where he began to present increased vertigo in the immediate transition from supine position to standing up, with a blood pressure of 70/42mmHg and heart rate of 135bpm. He performed dosage of aldosterone, renin and catecholamines in supine position and after 10 minutes in orthostatism. Laboratory results showed normal values of catecholamines, but they indicated a paradoxical increase of renin and aldosterone values, higher in supine position, respectively 201,4microUI/ml and 21,80ng/dl. A diagnosis of POTS was made and the therapy with fludrocortisone acetate at dose of 0,05mg/die was started.

At demission our patient was good and, at first follow-up, the laboratory values did not show the paradoxical increase of renin and aldosterone.

Discussion and conclusion: The management of POTS paediatric patients is very controversial, because of lack of trial studies. A complete clinical and diagnostic evaluation can provide the basis for a right management, based on syndrome's pathophysiology. In our case, we identified a hypovolemic form, so we expanded plasma volume with fludrocortisone, an aldosterone analogue, that increases sodium retention from the tubular fluid into the plasm. This empirical approach has allowed our patient a gradual recovery of his activities.

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