<abstract xmlns="http://www.w3.org/1999/xhtml"><sec id="j_jccm-2019-0023_s_005_w2aab3b7b5b1b6b1aab1c18b1Aa"><h3>Introduction</h3><p>Organophosphorus poisoning is the most common poison used for suicidal attempt in Nepal. Diabetes insipidus is unusual and rare in this poisoning. This is the second case report of Diabetes insipidus developing in organophosphorus poisoning. Management of diabetes insipidus includes desmopressin and adequate fluid management.</p></sec><sec id="j_jccm-2019-0023_s_006_w2aab3b7b5b1b6b1aab1c18b2Aa"><h3>Case presentation</h3><p>A 34-year-old female patient accompanied by her father presented at the Emergency department with an alleged history of ingestion of unknown amount of chlorpyrifos, cypermethrin and quinalphos. On admission, she had a Glasgow Coma Scale (GCS) of 7/15. Her blood pressure was 110/60 mm Hg, pulse 54/min, respiratory rate 45/min and saturation 35% on room air, pinpoint pupil reactive to light and bilateral crepitations. She was immediately resuscitated with two litres of normal saline and intubated with a 7 mm endotracheal tube. Atropinisation was done, and pralidoxime was started. She developed a urine output of 250-350 ml per hour with rising sodium and serum osmolality. The urine examination showed low sodium and urine specific gravity. A diagnosis of diabetes insipidus was made. There was no immediate improvement in her GCS. She was managed with 5% dextrose and subcutaneous desmopressin and was transferred out of the intensive care unit on the sixth day and was discharged from hospital on the fifteenth day.</p></sec><sec id="j_jccm-2019-0023_s_007_w2aab3b7b5b1b6b1aab1c18b3Aa"><h3>Conclusion</h3><p>Diabetes insipidus is a rare transient complication in organophosphorus poisoning that requires careful observation and early management with desmopressin and adequate fluid balance to improve patient outcome.</p></sec></abstract>

IntroductionOrganophosphorus poisoning is the most common poison used for suicidal attempt in Nepal. Diabetes insipidus is unusual and rare in this poisoning. This is the second case report of Diabetes insipidus developing in organophosphorus poisoning. Management of diabetes insipidus includes desmopressin and adequate fluid management.Case presentationA 34-year-old female patient accompanied by her father presented at the Emergency department with an alleged history of ingestion of unknown amount of chlorpyrifos, cypermethrin and quinalphos. On admission, she had a Glasgow Coma Scale (GCS) of 7/15. Her blood pressure was 110/60 mm Hg, pulse 54/min, respiratory rate 45/min and saturation 35% on room air, pinpoint pupil reactive to light and bilateral crepitations. She was immediately resuscitated with two litres of normal saline and intubated with a 7 mm endotracheal tube. Atropinisation was done, and pralidoxime was started. She developed a urine output of 250-350 ml per hour with rising sodium and serum osmolality. The urine examination showed low sodium and urine specific gravity. A diagnosis of diabetes insipidus was made. There was no immediate improvement in her GCS. She was managed with 5% dextrose and subcutaneous desmopressin and was transferred out of the intensive care unit on the sixth day and was discharged from hospital on the fifteenth day.ConclusionDiabetes insipidus is a rare transient complication in organophosphorus poisoning that requires careful observation and early management with desmopressin and adequate fluid balance to improve patient outcome.


<div xmlns="http://www.w3.org/1999/xhtml"><sec id="j_jccm-2019-0023_s_001_w2aab3b7b5b1b6b1ab1aAa"><div>Introduction</div><p>Organophosphorus (OP) poisoning with diethyl phosphoryl chloride compound is most common over the counter poison available in Nepal. [<a ref-type="bibr" href="#j_jccm-2019-0023_ref_001_w2aab3b7b5b1b6b1ab1b5b1Aa">1</a>, <a ref-type="bibr" href="#j_jccm-2019-0023_ref_002_w2aab3b7b5b1b6b1ab1b5b2Aa">2</a>, <a ref-type="bibr" href="#j_jccm-2019-0023_ref_003_w2aab3b7b5b1b6b1ab1b5b3Aa">3</a>] It causes acetylcholinesterase inhibition leading to acute cholinergic crisis and manifests as nicotinic, muscarinic and central nervous system effects [<a ref-type="bibr" href="#j_jccm-2019-0023_ref_004_w2aab3b7b5b1b6b1ab1b5b4Aa">4</a>].</p><p>Antidiuretic hormone (ADH) is synthesized at the supraoptic and paraventricular nuclei and released in response to plasma osmolality and circulating blood volume and act at collecting tubules to absorb water and to maintain osmolality and blood volume. Diabetes insipidus (DI) can be central or nephrogenic and occurs due to the absence, decrease, or unresponsiveness of ADH. Diabetes insipidus (DI) is a rare and unusual complication of OP poisoning. Previously, a case report of DI following malathion poisoning has been reported [5], but this is the first case report of DI as a result of diethyl compound ingestion.</p></sec><sec id="j_jccm-2019-0023_s_002_w2aab3b7b5b1b6b1ab1b1Aa"><div>Case Presentation</div><p>A 38 years old female weighing sixty kilograms, without any significant past medical or surgical history, accompanied by her father, presented at the emergency department of the General Superspeciality Hospital, Birtamode, Nepal after being referred by a primary physician from a local hospital<sup></sup>. She had ingested an unknown amount of chlorpyrifos, cypermethrin and quinalphos, six hours previously, allegedly to commit suicide.</p><p>At the time of admission to the emergency department, her GCS was 7/15, and her pupils were pinpoint reactive to light. Her pulse rate was 54 beats per min, blood pressure 110/60 mmHg, respiratory rate 45 breaths/min and oxygen saturation 35% on 15 litres of oxygen. Chest bilateral crepitations and wheezes were present on chest auscultation. Cardiovascular and abdominal examinations were normal. Arterial blood gas analysis showed pH 7.35, partial pressure of oxygen (PaO<sub>2</sub>) 46mm Hg; partial pressure of carbon dioxide (PaCO<sub>2</sub>) 31 mm Hg; lactate six mmol/ L and bicarbonate 18 mEq/ L. A diagnosis was made of Type 1 respiratory failure with metabolic and lactic acidosis.</p><p>An emergency physician and paramedics immediately resuscitated her by inserting a 16 gauze cannula, central venous catheter and giving two litres of normal saline. Intubation was undertaken with 7mm endotracheal tube.</p><p>The Peradeniya Organophosphorus Poisoning (POP) scale was 8. Gastric lavage was achieved with sixty grams activated charcoal and two litres of normal saline, seven-hour after the ingestion of the organophosphorus compound.</p><p>An atropine challenge test was carried. One ml of atropine being positive which was evidenced by an increase in heart rate by more than 25 beats per minute, from 58 to 90 beats per minute, and atropinisation was attained at 50 ml of atropine and atropine infusion was started at 5 ml/ hour. Pralidoxime chloride (Troikaa Pharmaceuticals Ltd., Ahmedabad, India) was started at one gram every six hours, according to the hospital protocol.</p><p>Her investigation profiles were total leucocyte count (TLC) - 13000/mm<sup>3</sup>; platelets-140000/mm<sup>3</sup>; haemoglobin (Hb)-9gm/dl; urea-58 mg/dl; creatinine-1.3 mg/ dl; sodium and potassium were 137 mmol/L and 3.9 mmol/ L, respectively. Liver function test was normal except for alanine aminotransferase, which was 96 U/ L. A chest x-Ray showed bilateral infiltrates. Serum acetylcholinesterase and RBC cholinesterase measurements were not obtained as these tests were not available in the hospital at the time.</p><p>The patient was managed with full ventilatory support. Atropine (Hindustan Medicines Pvt. Ltd., Barauni, India) infusion was started at 5 ml/ hr intravenously, pralidoxime (Troikaa Pharmaceuticals Ltd., Ahmedabad, India) one gram intravenously every six hours, piperacillin-tazobactam (Aristo Pharmaceuticals Pvt. Ltd., Mandideeep, India) 4.5g intravenously every eight hours. Routine monitoring of vital signs, input and output charting to attain a positive intake to output balance and ulcer protection with intravenous ranitidine (Cadilla Pharmaceutical, Ahmedabad, India) 50 mg every eight hours were carried out.</p><p>She developed a urine output of 250-300 ml/hour four hours after admission to the ICU, and there was no improvement in her GCS. The urine output remained constant for the next six hours and by twenty-four hours she had passed a total of six litres.</p><p>Based on the urine specific gravity of 1.001, urine osmolality 200 mOsm/kg, serum sodium 158 mEq/L and plasma osmolality 322mOsm/kg, a diagnosis of DI was made. Serum ADH was not measured.</p><p>Starting from the second hospital day, fluid management was accomplished by 5% dextrose intravenously, at a rate of 100 ml/hour and injection. Vasopressin, six units subcutaneously was given as an initializing dose. Desmopressin was not unavailable at the hospital pharmacy during that time.</p><p>She responded briefly for two hours after which a high urine output restarted. Strict fluid input and output charting was done to avoid negative balance, and serum sodium and potassium were measured every six hours. On the following day, urine output was 7 litres/day.</p><p>Desmopressin (Sun Pharmaceutical Industries Ltd., Mumbai, India), which had been imported from India, and was started at 100 micrograms, and two puffs were to be given when the urine output was more than 250 ml per hour for consecutive 3 hours. The treatment resulted in a decrease in urine output from 165mEq/L to 150 ml/ hr, serum sodium of 160 mEq/L. Her GCS improved from 7/15 to 13/15.</p><p>On the second day after admission, the patient developed a fever with her temperature ranging from 37.5<sup>o</sup>C to 39<sup>o</sup>C. Progressive infiltrates were observed on chest radiographs taken over the next two days (<a ref-type="fig" href="#j_jccm-2019-0023_fig_001_w2aab3b7b5b1b6b1ab1b1c14Aa">Figure 1</a>). A thick tracheal aspiration was noted and was sent for culture and sensitivity. Ventilator-associated pneumonia was confirmed. The culture of the tracheal aspiration revealed <italic>Klebsiella pneumoniae</italic> sensitive to polymyxin B and chloramphenicol and resistant to meropenem, amikacin, ampicillin, levofloxacin and imipenem.</p><figure id="j_jccm-2019-0023_fig_001_w2aab3b7b5b1b6b1ab1b1c14Aa" position="float" fig-type="figure"><h2>Fig. 1</h2><figCaption><p>Chest radiograph on the fourth hospital day. The image shows bilateral infiltrates due to ventilator-associated pneumonia.</p></figCaption><img xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="graphic/j_jccm-2019-0023_fig_001.jpg" src="https://sciendo-parsed.s3.eu-central-1.amazonaws.com/64720d53215d2f6c89dba300/j_jccm-2019-0023_fig_001.jpg?X-Amz-Algorithm=AWS4-HMAC-SHA256&amp;X-Amz-Date=20240601T201018Z&amp;X-Amz-SignedHeaders=host&amp;X-Amz-Expires=18000&amp;X-Amz-Credential=AKIA6AP2G7AKP25APDM2%2F20240601%2Feu-central-1%2Fs3%2Faws4_request&amp;X-Amz-Signature=32e08a21c302e2bdbf7d55617c5ff695dcc640d7aabd45c2b1f0472900b71e0a" class="mw-100"/></figure><p>The patient subsequently showed a decrease in urine output, serum sodium and improvement in her GCS over the next period of five days.</p><p>Piperacillin-tazobactam was stopped, and on the fifth day after admission, the patient was prescribed polymyxin B (Health Biotech Limited, Chandigarh, India) 1,500,000 units intravenously, then 1,000,000 units every twelve hours plus chloramphenicol (Biochem Pharmaceutical Industries, Mumbai, India, one gram every six hours.</p><p>With improving GCS and chest condition, she was extubated on the fifth day after admission and was moved from ICU on the sixth day after admission. Atropine was decreased by 10-20% every day and was stopped on the tenth days after admission. Her urine output (<a ref-type="fig" href="#j_jccm-2019-0023_fig_002_w2aab3b7b5b1b6b1ab1b1c18Aa">Figure 2</a>) and serum sodium (<a ref-type="fig" href="#j_jccm-2019-0023_fig_003_w2aab3b7b5b1b6b1ab1b1c19Aa">Figure 3</a>) were normal on the twelfth day after admission.</p><figure id="j_jccm-2019-0023_fig_002_w2aab3b7b5b1b6b1ab1b1c18Aa" position="float" fig-type="figure"><h2>Fig. 2</h2><figCaption><p>Urine output during hospital stay</p></figCaption><img xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="graphic/j_jccm-2019-0023_fig_002.jpg" src="https://sciendo-parsed.s3.eu-central-1.amazonaws.com/64720d53215d2f6c89dba300/j_jccm-2019-0023_fig_002.jpg?X-Amz-Algorithm=AWS4-HMAC-SHA256&amp;X-Amz-Date=20240601T201018Z&amp;X-Amz-SignedHeaders=host&amp;X-Amz-Expires=18000&amp;X-Amz-Credential=AKIA6AP2G7AKP25APDM2%2F20240601%2Feu-central-1%2Fs3%2Faws4_request&amp;X-Amz-Signature=156f470cdacf13216e1ceef35c2490de54c7accdde2d1e81f4800d34a339e375" class="mw-100"/></figure><figure id="j_jccm-2019-0023_fig_003_w2aab3b7b5b1b6b1ab1b1c19Aa" position="float" fig-type="figure"><h2>Fig. 3</h2><figCaption><p>Serum sodium during hospital stay</p></figCaption><img xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="graphic/j_jccm-2019-0023_fig_003.jpg" src="https://sciendo-parsed.s3.eu-central-1.amazonaws.com/64720d53215d2f6c89dba300/j_jccm-2019-0023_fig_003.jpg?X-Amz-Algorithm=AWS4-HMAC-SHA256&amp;X-Amz-Date=20240601T201018Z&amp;X-Amz-SignedHeaders=host&amp;X-Amz-Expires=18000&amp;X-Amz-Credential=AKIA6AP2G7AKP25APDM2%2F20240601%2Feu-central-1%2Fs3%2Faws4_request&amp;X-Amz-Signature=15811b3d07d5585cd8aff59d18b65cf0477fd9a92bd3dc64818698d1125ecdc6" class="mw-100"/></figure><p>She was discharged from hospital on the fifteenth hospital day.</p><p>One week following discharge, she presented at the outpatient department for a follow-up. Her sodium and potassium levels were 138 mEq/L and 3.9 mEq/L, respectively. She had also charted her urine output at her home, which was in the range of 2 to 2.5 litres/day.</p></sec><sec id="j_jccm-2019-0023_s_003_w2aab3b7b5b1b6b1ab1b2Aa"><div>Discussion</div><p>The neurologic manifestation of OP includes confusion, agitation, coma and seizure. The neurologic symptom of OP, atropine overdose and DI are similar that often leads to misdiagnosis. Diabetes insipidus in OP is rare, and the incidence is not known.</p><p>Diabetes insipidus can be central or nephrogenic. Our patient had central DI as the patient responded after desmopressin. There have been a few case reports of central DI following malathion [<a ref-type="bibr" href="#j_jccm-2019-0023_ref_005_w2aab3b7b5b1b6b1ab1b5b5Aa">5</a>], glufosinate [<a ref-type="bibr" href="#j_jccm-2019-0023_ref_006_w2aab3b7b5b1b6b1ab1b5b6Aa">6</a>], carbon monoxide [<a ref-type="bibr" href="#j_jccm-2019-0023_ref_007_w2aab3b7b5b1b6b1ab1b5b7Aa">7</a>] poisoning and overdose of baclofen and quetiapine [<a ref-type="bibr" href="#j_jccm-2019-0023_ref_008_w2aab3b7b5b1b6b1ab1b5b8Aa">8</a>] but there has been no case report following diethyl compound of OP. Central DI is common following pituitary surgery, tumour, infections, granulomas, inflammatory condition, vascular, chemical toxin and genetic but 50% is idiopathic [<a ref-type="bibr" href="#j_jccm-2019-0023_ref_009_w2aab3b7b5b1b6b1ab1b5b9Aa">9</a>], and our patient did not any of these causes.</p><p>Studies have shown that central DI usually appears within 24 hours of a CNS insult and lasts for 2-3 weeks. It rarely persists for more than three months [<a ref-type="bibr" href="#j_jccm-2019-0023_ref_009_w2aab3b7b5b1b6b1ab1b5b9Aa">9</a>]. Diagnosis is confirmed by urine and plasma osmolality, urine output and serum sodium levels.</p><p>Mechanism of action of DI in OP poisoning is not known. The possible reason may be that OP may temporarily damage hypothalamus and pituitary, causing transiently decrease or absence of ADH. Therefore, a large-scale study is required to explore the cause of DI in OP.</p><p>The treatment of central DI is to correct the underlying cause and fluid management. Studies have shown that vasopressin [<a ref-type="bibr" href="#j_jccm-2019-0023_ref_010_w2aab3b7b5b1b6b1ab1b5c10Aa">10</a>] can also be used instead of desmopressin, but vasopressin has a shorter duration of action than desmopressin, 5% dextrose or 0.5% normal saline is used for fluid management but in our patient 5% dextrose was used.</p></sec><sec id="j_jccm-2019-0023_s_004_w2aab3b7b5b1b6b1ab1b3Aa"><div>Conclusion</div><p>Diabetes insipidus following organophosphorus poisoning is rare and requires a high degree of suspicion and timely referral to a higher centre in order to decrease mortality and improve patient outcome.</p></sec></div>

Transient Diabetes Insipidus Following Organophosphorus Poisoning

The Journal of Critical Care Medicine

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

{"article-title":"Transient Diabetes Insipidus Following Organophosphorus Poisoning"}

IntroductionOrganophosphorus poisoning is the most common poison used for suicidal attempt in Nepal. Diabetes insipidus is unusual and rare in this poisoning....

Transient Diabetes Insipidus Following Organophosphorus Poisoning

Article Category: Case report

Published Online: Nov 27, 2019

Page range: 145 - 148

Received: Jul 10, 2019

Accepted: Sep 23, 2019

DOI: https://doi.org/10.2478/jccm-2019-0023

Keywords
diabetes insipidus, desmopressin, organophosphorus, urine

© 2019 Niraj Kumar Keyal, Amid Bhujel, published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

Fig. 1

Fig. 2

Fig. 3

Transient Diabetes Insipidus Following Organophosphorus Poisoning

Article Category: Case report

Published Online: Nov 27, 2019

Page range: 145 - 148

Received: Jul 10, 2019

Accepted: Sep 23, 2019

DOI: https://doi.org/10.2478/jccm-2019-0023

Keywordsdiabetes insipidus, desmopressin, organophosphorus, urine

© 2019 Niraj Kumar Keyal, Amid Bhujel, published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

Fig. 1

Fig. 2

Fig. 3

Keywords
diabetes insipidus, desmopressin, organophosphorus, urine