2023年7月9日 星期日

Current Ten Clinical Studies on New Psychoactive Substances in Taiwan

 

Year

Journal

University, Hospital.

Finding, Conclusion

Reference

2016

Subst Abuse Treat Prev Policy

Kaohsiung Medical University

Controlled NPS items in Taiwan were far less than those in Korea, but the quantity of total NPS seizures, especially with ketamine, was much larger in Taiwan than in Korea.

1

2017

Forensic Sci Int

Kaohsiung Medical University

Japan is the most proactive country in terms of the NPS regulation with 41% of the total number of controlled NPS in Northeast Asia, followed by South Korea (21%), China (28%), Taiwan (10%)

2

2020

J Formos Med Assoc

National Taiwan University Hospital

The most common NPS was ketamine (21.7%), followed by synthetic cathinones (14.8%).

Polysubstance use was more common in the NPS group than in the traditional group. Most patients were men (78.3%)

3

2022

Clin Toxicol (Phila)

.

Linkou Chang Gung Memorial Hospital

The most frequently detected drug was methamphetamine/amphetamine, followed by synthetic cathinones, ketamine and its two analogs, and opioids. Younger patients and women were more likely to have NPS detected in their urine samples. NPS-positive cases frequently experienced chest pain  tachycardia and suicide attempt/non-suicidal self-harm  whereas depressed consciousness was less frequent among NPS-positive cases than among other illicit drug-positive cases.

4

2022

J Formos Med Assoc

National Taiwan University College of Medicine

546 (73.7%) men and 195 (26.3%) women were enrolled. Compared to men, women were younger (32.03 ± 10.86 vs. 36.51 ± 10.84 years, p < 0.001) and more likely to use new psychoactive substances (NPS). Men were more likely to have HIV infection, whereas women were more likely to report psychiatric comorbidities. Women were less likely to have aggressive behaviors. The likelihood of rhabdomyolysis and intensive care unit admission was higher in men (p < 0.001).

5

2022

Clin Toxicol (Phila)

National Taiwan University College of Medicine

Tachycardia, hyperthermia, and rhabdomyolysis were more common among cathinone users than among meth/amphetamine users presented to EDs.

6

2022

J Formos Med Assoc

Taipei City Hospital

High suicidality and high psychiatric comorbidities in multiple illicit drug users call for special need for suicide screening and a more integrated care incorporating psychiatric and substance treatment.

7

2022

Toxics

Linkou Chang Gung Memorial Hospital

The mortality NPS users were older, with deep coma, faster heart rate and respiratory rate, lower blood pressures and O2 room air saturation, more seizures, abnormal breath sounds, and had urine incontinence compared to the survivor patients. The mortality patients also had acute kidney injury, higher potassium, blood sugar, liver function test, and lactate level.

8

2023

J Forensic Leg Med

Mackay Memorial Hospital

NPS users are relatively younger, are more likely to experience facial flush and palpitation and engage in more self-harm, violence, and suicide than non-NPS drug users.

9

2023

Medicine (Baltimore)

MacKay Memorial Hospital

The NPS users were significantly younger than those with negative results on toxic testing (26.4 vs 37.5, P = .005). The heart rate of NPS users was significantly faster than that of the group with negative results of toxic testing (111.1 vs 93.5 beats per minute, P = .046). The heartbeats of INPS group were also significantly faster than those with a negative result in toxicology screen (119.6 vs 93.5 beats per minute, P = .024). Those who used classical illicit drugs combined with NPS had significantly higher palpitation than those with negative results of toxic testing (27.3% vs 3.1%, P = .017).

10

1.      https://pubmed.ncbi.nlm.nih.gov/27663984/

2.      https://pubmed.ncbi.nlm.nih.gov/28088088/

3.      https://pubmed.ncbi.nlm.nih.gov/32037264/

4.      https://pubmed.ncbi.nlm.nih.gov/35315299/

5.      https://pubmed.ncbi.nlm.nih.gov/35365378/

6.      https://pubmed.ncbi.nlm.nih.gov/35438590/

7.      https://pubmed.ncbi.nlm.nih.gov/35484001/

8.      https://pubmed.ncbi.nlm.nih.gov/35878292/

9.      https://pubmed.ncbi.nlm.nih.gov/36571928/

10.  https://pubmed.ncbi.nlm.nih.gov/37352073/

 

Edited by Yu-Jang Su July, 9, 2023 

2023年6月12日 星期一

Amphetamine poisoning

 Substance

  Amphetamine

 

 

Common name

  安仔, 安公子 [1]

 

 

Involving system and Presentation

-          CV: flushing, diaphoresis, hypertension, vasoconstriction, lung edema, heart failure, shock. Tachycardia [1]

-          Neuro and psychiatric: agitation, delusion, hyperactivity, tremor, delirium, rigidity, acute psychosis [2], paranoid schizophrenia, hallucination. [1] Toxic encephalopathy. [3].

-          Hyperthermia, rhabdomyolysis, myoglobinuria. [1]

-          Acute kidney injury. [1]

-          acute porphyria. [4].

 

 

Antidote / Treatment

-          ACLS or shock, arrhythmia, hypertension, tachycardia.

-          Intubation when respiratory failure [1]

-          GI decontamination within 1 hour. Activated charcoal, 1gm/kg with laxative agent [1]

-          Benzodiazepine, barbiturate for seizure, delirium. [1]

-          Fever: sedative and external cooling. [1]

-          Rhabdomyolysis – hydration to keep urine output 1—2 ml./kg BW/hour. [1]

-          VPC – benzodiazepine +/- lidocaine. [1]

-          - hypotension – fluid challenge or inotropic agent. [1]

 

Disposition

-          PCO2 ≥ 51 mmHg, serum bicarbonate ≤ 22.6 mEq/L, and loss of consciousness on admission could be considered as prognostic factors of mortality [5]

-          The mortality rate was 5.4% [5]

 

 

References

 

[1]急性中毒救命術 三版 急診 急診醫學會p.119-128.

 

[2]. Bramness JG, Rognli EB. Psychosis induced by amphetamines. Curr Opin Psychiatry. 2016 Jul;29(4):236-41. doi: 10.1097/YCO.0000000000000254. PMID: 27175554.

 

[3]. Bojsen JA, Lunau L, Nguyen NT, Rasmussen BSB. [Amphetamine-induced toxic encephalopathy]. Ugeskr Laeger. 2022 May 23;184(21):V12210924. Danish. PMID: 35656615.

 

 

[4]. Kiew CK, Lam ASEL. Unexpected presentation of acute porphyria. BMJ Case Rep. 2021 Jun 29;14(6):e241580. doi: 10.1136/bcr-2021-241580. PMID: 34187794; PMCID: PMC8245470.

 

[5] Rahimi M, Lookzadeh S, Sadeghi R, Soltaninejad K, Shadnia S, Pajoumand A, Hassanian-Moghaddam H, Zamani N, Latifi-Pour M. Predictive Factors of Mortality in Acute Amphetamine Type Stimulants Poisoning; a Review of 226 Cases. Emerg (Tehran). 2018;6(1):e1. Epub 2018 Jan 10. PMID: 29503826; PMCID: PMC5827041.

 

Edited by Yu-Jang Su June 12, 2023

 

2023年5月1日 星期一

Glufosinate

 Substance

 

Glufosinate-Ammonium 13.5%SL

 

Common name / Trade name

 

強手(固殺草); 草銨膦

 

Involving system

-          Mechanism: glutamine synthetase-inhibiting [1]

-          Interferes with glutamate synthetase activity [2]

-          Neurotoxicity.

-          Mental disturbances [3]

-          Hematological changes

-          Gastrointestinal effects [3], nausea.

 

Presentation

-          Altered mental status [4] amnesia [2]

-          Fever [2]

-          Arrhythmia, [2]

-          Seizure, 31.5% [5]

-          higher initial ammonia levels. [6]

-          respiratory failure. [7]

-          Vasogenic edema in striatum [8]

-          Shock [2]

 

Antidote and Treatment

-          Activated charcoal, Carbomix [2].

-          IVF, monitoring urine output.

-          Intubation if respiratory failure

-          Monitoring.

-           supportive care.

-           benzodiazepine for seizure

-          Without antidote.

-          Hemodialysis [2]

 

Disposition

-          Observe 48 hours, [2]

-          Age > 70 years and GCS score < 9 at triage could be predictors of mortality in patients. [4]

-          An initial serum ammonia level >151 µg/dL was an independent early predictor of in-hospital mortality [9]

-          Older age (≥ 61 years; adjusted OR 4.9) and larger amount of glufosinate ingestion (≥ 13.9 grams; adjusted OR 25.2) were positively associated with the development of severe toxicity [10].

-          6.1% to 17.7% died following deliberate glufosinate ingestion. [2, 10]

 

References

 

[1]. https://pubmed.ncbi.nlm.nih.gov/36963955/

[2].Goldfrank’s Toxicology Emergencies p1478—79. 11th ed.

[3] https://pubmed.ncbi.nlm.nih.gov/9491336/

[4] https://pubmed.ncbi.nlm.nih.gov/34392143/

[5]. https://pubmed.ncbi.nlm.nih.gov/28421825/

[6] https://pubmed.ncbi.nlm.nih.gov/36399183/

[7]. https://pubmed.ncbi.nlm.nih.gov/24044532/

[8] https://pubmed.ncbi.nlm.nih.gov/19581091/

[9]. https://pubmed.ncbi.nlm.nih.gov/31146590/

[10] https://pubmed.ncbi.nlm.nih.gov/22480254/

 

Edited by Yu-Jang Su May 1st, 2023. 

2023年4月12日 星期三

Inoxicated / Poisoning-Related Coma Blister

 

Inoxicated / Poisoning-Related Coma Blister

Year

Country

Age

Gender

Substance

References

2022

US

82

F

lorazepam for insomnia

1

2012

Brazil

45

F

clonazepam, promethazine, oxcarbazepine and quetiapine

2

2009

UK

 

 

barbiturate

3

2007

UK

53

F

Acetaminophen 500mg, codeine 30mg

4

2002

Germany

 

 

theophylline toxicity

5

2002

Canada

 

 

amitriptyline overdose

6

1991

Australia

25

M

carbon monoxide

7

1990

Ichilov

75

 

200 mg oxazepam

8

1972

 

 

 

BARBITURATE

9

1.      https://pubmed.ncbi.nlm.nih.gov/35180064/

2.      https://pubmed.ncbi.nlm.nih.gov/22892778/

3.      https://pubmed.ncbi.nlm.nih.gov/19359256/

4.      https://pubmed.ncbi.nlm.nih.gov/17952753/

5.      https://pubmed.ncbi.nlm.nih.gov/12198361/

6.      https://pubmed.ncbi.nlm.nih.gov/12447625/

7.      https://pubmed.ncbi.nlm.nih.gov/1743385/

8.      https://pubmed.ncbi.nlm.nih.gov/2231838/

9.      https://pubmed.ncbi.nlm.nih.gov/4116178/

 edited by Yu-Jang Su  April 12, 2023. 

Ciguatoxins Poisoning

  Substance Ciguatoxins (CTXs) 雪卡毒素,又名雪卡魚毒素或西加魚毒素。   Common names Ciguatera toxins in 熱帶與亞熱帶的珊瑚礁魚類 Ciguatera fish toxins: resist...