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ISSN: 2329-6895
Journal of Neurological Disorders
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The Iced Drink Test - A Bedside Test for Diagnosis of Bulbar Myasthenia

Nishit Sawal*

Department of Medicine, Government Medical College and Hospital-Sector 32, Chandigarh, India

*Corresponding Author:
Nishit Sawal
Assistant Professor, Department of Medicine
Government Medical College and Hospital-Sector 32
Chandigarh, India
Tel: 0172-2601024
E-mail: [email protected]

Received date: March 06, 2017; Accepted date: March 16, 2017; Published date: March 21, 2017

Citation: Sawal N (2017) The Iced Drink Test - A Bedside Test for Diagnosis of Bulbar Myasthenia. J Neurol Disord 5:333. doi:10.4172/2329-6895.1000333

Copyright: © 2017 Sawal N. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Abstract

The diagnosis of Myasthenia gravis (MG) is chiefly based on clinical symptoms and neurological examination coupled with serological testing for the presence of auto-antibodies, electrodiagnostic studies consisting of repetitive nerve stimulation test (RNST) and single fiber electromyography (SFEMG) and pharmacologic tests such as the edrophonium test. The ice pack test, based on the scientific principle that cooling improves neuromuscular transmission in Myasthenia gravis (MG), is a low cost, sensitive and specific test used for differentiating myasthenic ptosis from other causes of ptosis.

Based on the same principle, we propose the iced drink test as a quick, bedside test for differentiating bulbar weakness caused by myasthenia gravis from other causes of lower motor neuron type of bulbar weakness. The iced drink test, if validated, can prove to be useful in quick diagnosis of bulbar myasthenia.

Keywords

Bulbar myasthenia; Diagnose; Electrophysiological testing; Ice pack; Safe bedside test

Introduction

Myasthenia gravis (MG) is the most frequently encountered neuromuscular junction (NMJ) disorder in clinical practice with a prevalence of 5 to 15 cases per 100,000 [1]. It is an autoimmune disease caused by antibodies directed against the nicotinic acetylcholine receptors (AChR) on the post synaptic membrane in 70% to 80% of patients [2] and in up to 40% of those patients negative for AChR antibodies, antibodies against the muscle specific Kinase (MuSK) can be demonstrated [3]. These antibodies produce impairment of normal NMJ function causing reduced or blocked transmission from the nerve to the muscle, producing weakness and fatigability.

Ocular symptoms in form of ptosis and/or diplopia are the presenting sign of the disease in 50% to 75% of patients [2]. Myasthenic patients can also present with isolated bulbar symptoms (20.73%) or bulbar plus ocular symptoms (23.17%). The voice can be affected with palatal weakness causing nasal voice and laryngeal weakness producing dysphonia. Dysarthria and dysphagia are seen, especially with tongue and/or lower facial weakness. Chewing weakness with difficulty chewing hard foods and fatigue with prolonged chewing is seen [4-6].

The diagnosis of MG is predominantly clinical aided by the presence of serum antibodies (e.g. AChR, MuSK) or abnormal electrodiagnostic studies which consist of repetitive nerve stimulation test (RNST) and single fiber electromyography (SFEMG). Another commonly used test is the edrophonium test which consists of injecting a short-lived inhibitor of acetylcholinesterase (AChE) to increase the availability of acetylcholine at the NMJ. This produces a quick and often dramatic improvement in the symptoms or signs of MG (e.g. ptosis, dysphonia) [7].

Another commonly used bedside test is the ice pack test for ptosis. The test consists of the application of ice to the eyes for 2–5 min with myasthenic ptosis improving after cooling. The sensitivity and specificity of the ice pack test in ocular myasthenia associated or not with generalized symptoms has been reported in various studies as varying from 80% to 100% [8-11]. Using the same principle of improvement in neuromuscular transmission at the neuromuscular junction (NMJ) with cooling, we propose a novel test - the iced drink test for bedside diagnosis of bulbar myasthenia.

Case Report

A 42-year-old male, working as a college lecturer presented to Neurology OPD with symptoms of dysphonia and dysphagia which were of gradual subacute onset since the past 8-10 days. Patient had noticed he had difficulty eating digestive biscuits (biscuits which contain wheat flour/bran/fiber and added roughage and are claimed by manufacturers to have less calories than the regular ones), he felt as if they got stuck in his throat and he had to wash them down with a sip of water. His wife had noticed a slight nasal twang to his voice since the same duration and slight lowering of loudness of voice. Patient had no chewing difficulty (He had eaten chicken thrice during the mentioned period without any difficulty), no ptosis, diplopia or neck weakness and had not noticed a diurnal pattern to his symptoms and did not report fatigability. Patient was a non-diabetic, non-hypertensive, non smoker and there was no history of any other substance abuse. There was no history of recent insect bite or vaccination. There was no history of any throat illness. Past medical history was unremarkable. Family history was unremarkable.

On neurological examination, tone and power was normal in all muscles, tongue power tested by having patient push his cheek from inside against resistance) was normal, tongue tone was normal. All reflexes were normal, jaw jerk was absent, gag reflex was slightly diminished and there was a slight nasal twang to his voice (Since the neurologist was seeing the patient for the first time, this was more on testimony of his wife and sister-the nasal twang was not very marked). There was no tongue atrophy and no fasciculations. Rest of neurological examination was unremarkable.

A provisional clinical diagnosis of subacute onset lower motor neuron (LMN) type bulbar pathology was made and differential diagnosis’s entertained as per neural axis localization were at level of nerve (polyneuritis cranialis) and NMJ (Mysathenia gravis). Initially a formal 30 ml water swallow test of a patient was carried out [12]. This was normal and he could easily gulp down water without any regurgitation or choking. Patient’s voice was evaluated by making his wife stand at 15 meters from the patient in the hospital corridor and his younger sister at 30 meters and the patient was asked to say certain words (10 words) and some short sentences. His wife and sister were asked to evaluate the loudness and nasal twang of his voice. Patient was then given a glass of iced water, more than half of glass was filled with crushed ice and rest with cold water and patient was asked to sip it, swirl in his mouth and also do gargles with the iced water. He was asked to do so for 4-5 min and then he was again asked to say the same words (10 words) and same short sentences. His wife and sister again evaluated the loudness and nasal twang of his voice at 15 and 30 meters.

Post the iced water intervention, the patient, his wife and sister all concurred that there was a significant improvement in both the parameters being evaluated. There was an increase in loudness and the nasal twang disappeared. We also noticed that his nasal twang almost disappeared post the iced drink test only to reappear after some time. Keeping the possibility of myasthenia now on top of differential diagnosis’s, an acetylcholine receptor antibody assay was obtained which came out to be positive. The patient refused to give consent for both the repetitive nerve stimulation test (RNST) as well as the edrophonium test. MRI-brain and cervical spine was done to exclude any mimics and was normal. Laryngoscopic examination was normal. Chest X-ray was normal. CT-Thorax is duly scheduled. Patient was put on pyridostigmine and corticosteroids and reported improvement of symptoms with treatment. Next follow up with CT-Thorax is due shortly. Further therapeutic plan is to assess patient for thymectomy and to taper off steroids and add appropriate steroid sparing agent.

Discussion

Clinical history and neurological examination form the bedrock of diagnosis of myasthenia gravis. In addition, tests used to confirm the clinical diagnosis include the edrophonium test, electrophysiological studies, ice pack test for myasthenic ptosis and serological tests for auto-antibodies [7]. The icepack test has a sensitivity and specificity of 80% to 100% [8-11]. It is a cheap, safe, quick to perform useful bedside test with no false-positives reported [11]. Studies showed improved neuromuscular junction transmission in myasthenia with cooling [13-15]. This is owing to lesser acetylcholinesterase activity at temperatures below 28°C, providing increasing amount of acetylcholine molecules in the synaptic cleft by decreasing the hydrolysis rate of acetylcholine molecules in the synaptic cleft [15]. Based on these studies, local cooling by application of ice pack was proposed as a simple procedure for the diagnosis of ocular myasthenia [16]. Numerous subsequent studies have confirmed the diagnostic validity of this test in the evaluation of ocular myasthenia which has been found to have a high sensitivity and specificity of around 80% to 100% [8-11].

The currently used diagnostic tests for myasthenia other than the serological tests for auto-antibodies are invasive and have certain disadvantages. The edrophonium test can cause complications like cardiac arrhythmias, respiratory failure and seizures. Resuscitation facilities should always be available while carrying out the test and requires continuous patient monitoring [17,18]. The electrodiagnostic studies which consist of repetitive nerve stimulation test (RNST) and single fiber electromyography (SFEMG) also have their limitations. SFEMG is the most sensitive technique but it is invasive and employs a needle electrode, requires special equipment and training and is timeand labor-intensive [19,20], and is not widely available in developing countries. SFEMG also has the potential of causing hemorrhage, hematoma formation and infection. Since repetitive nerve stimulation test (RNST) is a painful procedure which involves supramaximal stimulation of a peripheral nerve to measure compound muscle action potential (CMAP) decrement with repetitive stimuli [21], it is poorly tolerated by some patients.

Conclusion

We have used the well known principle of cooling improving neuromuscular transmission in myasthenia to devise the iced drink test for bulbar myasthenia. We propose that the test be done only after carrying out a formal swallow test of the patient. If the patient fails the swallow test, the iced drink should not be carried out otherwise the patient may aspirate. If the patient has a normal swallow test, then only the iced drink test should be carried out. First a baseline evaluation of patient’s symptoms should be done so as to allow a rough objectification. Since our patient had reported a nasal twang with some lowering of loudness of voice, these were the parameters we chose to assess. The patient should be given a glass of iced water filled more than half with crushed ice. The patient should then be asked to sip it, swirl it in his mouth and to do gargles with the iced water so as to subject the oral cavity, the hard and soft palate and the pharynx to contact with ice cold water so as to cause local cooling for 4-5 min. Post the iced drink, the patient can again be asked to do the same activity done prior to the administration of the iced drink and improvement, if any should be noted. In developing countries where neurologists are very few [22], and have very busy OPD’s catering to a large number of patients every day, a simple, rapid, non-invasive, inexpensive test for rapid diagnosis of myasthenia can prove to be very useful. In addition, in developing countries electrodiagnostic studies like RNST and SFEMG are usually available only in select centers, are expensive tests and usually come with a long waiting period. Moreover invasive tests like the edrophomium test which involve a short term hospital admission and can cause serious side effects are also cumbersome to carry out. In this scenario, the iced drink test, if it proves to be of value in MG in a properly designed study, can prove to be of value. The iced drink test may be helpful to guide the next line of investigations. eg. If a patient presenting with bulbar symptoms has a positive iced water test, one can straightway proceed to a RNST/SFEMG and serological testing for AChR antibodies with higher degree of confidence. I propose this novel iced drink test as a quick, safe, inexpensive way to diagnose bulbar myasthenia. More studies however are needed before this test can be accepted in clinical practice.

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