Spectrum of hypokalemic paralysis from a tertiary care center in India
Hypokalemic paralysis is an important and reversible cause of acute flaccid paralysis. The treating physician faces unique diagnostic and therapeutic challenges. We did a prospective study and included all patients with acute flaccid weakness and documented serum potassium of <3.5 mEq/L during th...
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doaj-6300927f26804ea795ce264af33098d02020-11-24T21:02:16ZengWolters Kluwer Medknow PublicationsIndian Journal of Nephrology0971-40651998-36622018-01-0128536536910.4103/ijn.IJN_225_17Spectrum of hypokalemic paralysis from a tertiary care center in IndiaG ChandramohanT DineshkumarR ArulM SeenivasanJ DhanapriyaR SakthirajanT BalasubramaniyanN Gopalakrishnan1Hypokalemic paralysis is an important and reversible cause of acute flaccid paralysis. The treating physician faces unique diagnostic and therapeutic challenges. We did a prospective study and included all patients with acute flaccid weakness and documented serum potassium of <3.5 mEq/L during the period between January 2009 and August 2015. We studied the incidence, etiology, clinical profile, and acid–base disturbances in patients presenting with hypokalemic paralysis and analyzed the significance of periodic and non-periodic forms of hypokalemic paralysis on patient's outcome. Two hundred and six patients were studied with a mean follow-up of 3.6 ± 1.2 years. Mean age was 37.61 ± 2.2 years (range 18–50 years). Males were predominant (M:F ratio 2.1:1). The nonperiodic form of hypokalemic paralysis was the most common (61%). Eighty-one (39%) patients had metabolic acidosis, 78 (38%) had normal acid–base status, and 47 (23%) patients had metabolic alkalosis. The most common secondary cause was distal renal tubular acidosis (RTA) (n = 75, 36%), followed by Gitelman syndrome (n = 39, 18%), thyrotoxic paralysis (n = 8, 4%), hyperaldosteronism (n = 7, 3%), and proximal RTA (n = 6, 4%). Patients with non-periodic paralysis had more urinary loss (40.1 vs. 12.2 mmol, P = 0.04), more requirement of potassium replacement (120 vs. 48 mmol, P = 0.05), and longer recovery time of weakness (48.1 vs. 16.5 h, P = 0.05) than patients with periodic paralysis. Non-periodic form of hypokalemic paralysis was the most common variant in our study. Patients with periodic paralysis had significant incidence of rebound hyperkalemia.http://www.indianjnephrol.org/article.asp?issn=0971-4065;year=2018;volume=28;issue=5;spage=365;epage=369;aulast=ChandramohanAcute flaccid paralysisdistal renal tubular acidosisGitelman syndromehypokalemia |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
G Chandramohan T Dineshkumar R Arul M Seenivasan J Dhanapriya R Sakthirajan T Balasubramaniyan N Gopalakrishnan1 |
spellingShingle |
G Chandramohan T Dineshkumar R Arul M Seenivasan J Dhanapriya R Sakthirajan T Balasubramaniyan N Gopalakrishnan1 Spectrum of hypokalemic paralysis from a tertiary care center in India Indian Journal of Nephrology Acute flaccid paralysis distal renal tubular acidosis Gitelman syndrome hypokalemia |
author_facet |
G Chandramohan T Dineshkumar R Arul M Seenivasan J Dhanapriya R Sakthirajan T Balasubramaniyan N Gopalakrishnan1 |
author_sort |
G Chandramohan |
title |
Spectrum of hypokalemic paralysis from a tertiary care center in India |
title_short |
Spectrum of hypokalemic paralysis from a tertiary care center in India |
title_full |
Spectrum of hypokalemic paralysis from a tertiary care center in India |
title_fullStr |
Spectrum of hypokalemic paralysis from a tertiary care center in India |
title_full_unstemmed |
Spectrum of hypokalemic paralysis from a tertiary care center in India |
title_sort |
spectrum of hypokalemic paralysis from a tertiary care center in india |
publisher |
Wolters Kluwer Medknow Publications |
series |
Indian Journal of Nephrology |
issn |
0971-4065 1998-3662 |
publishDate |
2018-01-01 |
description |
Hypokalemic paralysis is an important and reversible cause of acute flaccid paralysis. The treating physician faces unique diagnostic and therapeutic challenges. We did a prospective study and included all patients with acute flaccid weakness and documented serum potassium of <3.5 mEq/L during the period between January 2009 and August 2015. We studied the incidence, etiology, clinical profile, and acid–base disturbances in patients presenting with hypokalemic paralysis and analyzed the significance of periodic and non-periodic forms of hypokalemic paralysis on patient's outcome. Two hundred and six patients were studied with a mean follow-up of 3.6 ± 1.2 years. Mean age was 37.61 ± 2.2 years (range 18–50 years). Males were predominant (M:F ratio 2.1:1). The nonperiodic form of hypokalemic paralysis was the most common (61%). Eighty-one (39%) patients had metabolic acidosis, 78 (38%) had normal acid–base status, and 47 (23%) patients had metabolic alkalosis. The most common secondary cause was distal renal tubular acidosis (RTA) (n = 75, 36%), followed by Gitelman syndrome (n = 39, 18%), thyrotoxic paralysis (n = 8, 4%), hyperaldosteronism (n = 7, 3%), and proximal RTA (n = 6, 4%). Patients with non-periodic paralysis had more urinary loss (40.1 vs. 12.2 mmol, P = 0.04), more requirement of potassium replacement (120 vs. 48 mmol, P = 0.05), and longer recovery time of weakness (48.1 vs. 16.5 h, P = 0.05) than patients with periodic paralysis. Non-periodic form of hypokalemic paralysis was the most common variant in our study. Patients with periodic paralysis had significant incidence of rebound hyperkalemia. |
topic |
Acute flaccid paralysis distal renal tubular acidosis Gitelman syndrome hypokalemia |
url |
http://www.indianjnephrol.org/article.asp?issn=0971-4065;year=2018;volume=28;issue=5;spage=365;epage=369;aulast=Chandramohan |
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