Journals / Eastern Journal of Medicine / 2019 / Cilt: 24 - Sayı: 3

Evaluation and Comparison of Patients Poisoned with Acetaminophen and Nonsteroidal Anti-Inflammatory Drugs

Pages
314–319
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Moreover, the acetylcysteine treatments in the early period of the acetaminophen toxicity are very effective in decreasing the mortality and morbidity.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:We aimed to determine and compare the clinical and demographical features, treatments, follow-up, poisoning scores and outcome of cases with the acetaminophen and NSAIDs intoxication.
📊
Key Findings & Data:Data of the patients who were at the age of 18 and older and applied to the Emergency Department with the acetaminophen or NSAIDs intoxication were retrospectively examined.
💡
Conclusion & Impact:Moreover, the acetylcysteine treatments in the early period of the acetaminophen toxicity are very effective in decreasing the mortality and morbidity.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

We aimed to determine and compare the clinical and demographical features, treatments, follow-up, poisoning scores and outcome of cases with the acetaminophen and NSAIDs intoxication. Data of the patients who were at the age of 18 and older and applied to the Emergency Department with the acetaminophen or NSAIDs intoxication were retrospectively examined. The cases were divided into 2 groups as the acetaminophen and NSAIDs group. The cases‟ age, gender, drug dose, hospitalization status and periods, poisoning scores (PSS, APACHE-II) and last conditions in discharging from the hospital were compared. The döşe was taken by 99 (55%) patients in the acetaminophen group was calculated as toxic, and intravenous acetylcysteine was administered to 70 (38.9%) patients as an antidote. When the APACHE-II scores of the patients hospitalized in the intensive care unit were examined, the mean APACHE-II score of 54 patients in the acetaminophen group was 3.15±3.70, the mean APACHE-II score of 34 patients in the NSAIDs group was 4.15±3.13 and it was statistically higher (p=0.031). All the patients followed-up in both groups were discharged with healing except only 1 (0.6%) patient who developed acute liver failure. Conclusion: The mean APACHE-II score was low in both groups. Therefore, following-up the patients in a unit such as a toxicology unit instead of the intensive care unit can be beneficial in terms of both reducing the place and labor force loads and cost. Moreover, the acetylcysteine treatments in the early period of the acetaminophen toxicity are very effective in decreasing the mortality and morbidity.

🔖

Cite This Article

ÇELİK, A., ŞAŞMAZ, M. İ. (2019). Evaluation and Comparison of Patients Poisoned with Acetaminophen and Nonsteroidal Anti-Inflammatory Drugs. Eastern Journal of Medicine, Cilt: 24 - Sayı: 3, 314–319. https://ajindex.com/articles/222584

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (14)

  1. Pierce CA, Voss B. Efficacy and safety of ibuprofen and acetaminophen in children and adults: a meta-analysis and qualitative review. Ann Pharmacother 2010; 44: 489-506
  2. Paulose-Ram R, Hirsch R, Dillon C, et al. Prescription and non-prescription analgesic use among the US adult population: results from the third National Health and Nutrition Examination Survey (NHANES III). Pharmacoepidemiol Drug Saf 2003; 12: 315-326
  3. Mowry JB, Spyker DA, Brooks DE, Zimmerman A, Schauben JL. Annual Report of the American Association of Poison Control Centers‟ National Poison Data System (NPDS): 33rd Annual Report. Clinical Toxicology 2015; 54: 924-1109
  4. Chung EY, Tat ST. Nonsteroidal antiinflammatory drug toxicity in children: a clinical review. Pediatric emergency care 2016; 32: 250- 253
  5. Burke A, Smyth E, FitzGerald GA. Analgesicantipyretic and antiinflammatory agents; pharmacotherapy of gout. Goodman & Gilman‟s The Pharmacological Basis of Therapeutics. 11th edn. McGraw Hill, San Diego, CA 2005; 671-716
  6. Masso Gonzalez EL, Patrignani P, Tacconelli S, et al. Variability among nonsteroidal antiinflammatory drugs in risk of upper gastrointestinal bleeding. Arthritis Rheum 2010; 62: 1592-1601
  7. Larson AM, Polson J, Fontana RJ, et al. Acetaminophen-induced acute liver failure: results of a United States multicenter, prospective study. Hepatology 2005; 42: 1364-1372
  8. Hinson JA, Roberts DW, James LP. Mechanisms of acetaminophen-induced liver necrosis. Handb Exp Pharmacol 2010; 369-405
  9. Antoine DJ, Jenkins RE, Dear JW, et al. Molecular forms of HMGB1 and keratin-18 as mechanistic biomarkers for mode of cell death and prognosis during clinical acetaminophen hepatotoxicity. J Hepatol 2012; 56: 1070-1079
  10. Lancaster EM, Hiatt JR, Zarrinpar A. Acetaminophen hepatotoxicity: an updated review. Arch Toxicol 2015; 89: 193-199
  11. Schmidt LE, Dalhoff K. Risk factors in the development of adverse reactions to N‐acetylcysteine in patients with paracetamol poisoning. British journal of clinical pharmacology 2001; 51: 87-91
  12. Kirschner RI, Rozier CM, Smith LM, Jacobitz KL. Nomogram line crossing after acetaminophen combination product overdose. Clinical toxicology 2016; 54: 40-46
  13. James LP, Letzig LG, Simpson PM, et al. Pharmacokinetics of acetaminophen protein adducts in adults with acetaminophen overdose and acute liver failure. Drug Metabolism and Disposition 2009
  14. Park BK, Dear JW, Antoine DJ. Paracetamol (acetaminophen) poisoning. BMJ clinical