Skip to main content
Erschienen in: Pediatric Nephrology 12/2021

04.10.2021 | Clinical Quiz

Solving an unusual case of acute kidney injury: Answers

verfasst von: Uttam Garg, Eugenio Taboada, Katherine L. Kurzinski, Clarence C. Frazee, Darcy K. Weidemann, Tarak Srivastava

Erschienen in: Pediatric Nephrology | Ausgabe 12/2021

Einloggen, um Zugang zu erhalten

Excerpt

1.
What is your most likely diagnosis?
Acute tubular necrosis due to ingestion of an unknown nephrotoxic agent.
 
2.
Which additional laboratory testing, if any, is required for definitive diagnosis?
A kidney biopsy is necessary to confirm the diagnosis of suspected acute kidney injury (AKI) due to ingestion of a nephrotoxic agent. The kidney biopsy demonstrated significant acute tubular injury with features of acute tubular necrosis on light microscopy (Figure 1) including irregular tubules with luminal dilation, necrosis, and detachment of tubular epithelial cells from the basement membrane with pyknotic nuclei and cytoplasmic vacuolation. The glomeruli, interstitium, and direct immunofluorescence was unremarkable.
Comprehensive drug screen can be helpful in identifying toxic agent(s). After further discussion of the biopsy results with the patient in private, he admitted to taking ~25–30 over-the-counter cough and cold medications to “get high” approximately 24 h prior to his presentation. Original urine and blood samples collected at our facility were then retrieved for additional analyses. An expanded urine drug screen for > 200 drugs was performed by gas chromatography–mass spectrometry (GC-MS) (Agilent Technologies, Santa Clara, CA). A large peak matching with dextromethorphan and a small peak matching with guaifenesin were detected and consistent with the patient’s reported ingestion. The blood sample with adequate volume collected 9 h after arrival to our hospital was sent to NMS laboratories (Willow Grove, PA) for dextromethorphan and guaifenesin quantification by liquid chromatography–tandem mass spectrometry. Concentrations of guaifenesin (therapeutic range, 0.3–1.4 mcg/mL) and dextromethorphan (therapeutic range, 10–40 ng/mL) were 0.13 mcg/mL and 290 ng/mL, respectively. Despite the significant time lapse between ingestion and specimen collection (estimated ~36 h), the dextromethorphan concentration was still well within the toxic range (toxic > 100 ng/mL).
 
3.
How would you manage this patient?
Due to worsening AKI with a rapid progression of BUN from 36 to 83 mg/dL and serum creatinine from 3.27 to 9.43 mg/dL in 36 h, a tunneled hemodialysis catheter was placed. The patient received a total of three sessions of hemodialysis. He required amlodipine and clonidine for hypertension. After 4 days of complete anuria, he began to experience kidney recovery. Laboratory testing on discharge 1 week from admission showed normal serum electrolytes with serum creatinine 1.21 mg/dL (Figure 2). He was discharged after receiving counseling for his drug ingestion with continued outpatient follow-up arranged for ongoing management of AKI and solitary kidney. Follow-up 3 weeks later demonstrated normal serum creatinine of 0.87 mg/dL and an unremarkable urinalysis, with normal urine protein/creatinine ratio of 0.09 mg/mgCr, and blood pressures well-controlled on amlodipine.
 
Literatur
1.
Zurück zum Zitat Levine DA (2007) “Pharming”: the abuse of prescription and over-the-counter drugs in teens. Curr Opin Pediatr 19:270–274CrossRef Levine DA (2007) “Pharming”: the abuse of prescription and over-the-counter drugs in teens. Curr Opin Pediatr 19:270–274CrossRef
2.
Zurück zum Zitat Karami S, Major JM, Calderon S, McAninch JK (2018) Trends in dextromethorphan cough and cold products: 2000–2015 National Poison Data System intentional abuse exposure calls. Clin Toxicol (Phila) 56:656–663CrossRef Karami S, Major JM, Calderon S, McAninch JK (2018) Trends in dextromethorphan cough and cold products: 2000–2015 National Poison Data System intentional abuse exposure calls. Clin Toxicol (Phila) 56:656–663CrossRef
4.
Zurück zum Zitat (2018) Drugs for cough. Med Lett Drugs Ther 60:206–268 (2018) Drugs for cough. Med Lett Drugs Ther 60:206–268
5.
Zurück zum Zitat Brown GR, McLaughlin K, Vaughn K (2018) Identifying and treating patients with synthetic psychoactive drug intoxication. JAAPA 31:1–5CrossRef Brown GR, McLaughlin K, Vaughn K (2018) Identifying and treating patients with synthetic psychoactive drug intoxication. JAAPA 31:1–5CrossRef
6.
Zurück zum Zitat Dy P, Arcega V, Ghali W, Wolfe W (2017) Serotonin syndrome caused by drug to drug interaction between escitalopram and dextromethorphan. BMJ Case Rep 2017:bcr2017221486 Dy P, Arcega V, Ghali W, Wolfe W (2017) Serotonin syndrome caused by drug to drug interaction between escitalopram and dextromethorphan. BMJ Case Rep 2017:bcr2017221486
7.
Zurück zum Zitat Small E, Sandefur BJ (2014) Acute renal failure after ingestion of guaifenesin and dextromethorphan. J Emerg Med 47:26–29CrossRef Small E, Sandefur BJ (2014) Acute renal failure after ingestion of guaifenesin and dextromethorphan. J Emerg Med 47:26–29CrossRef
8.
Zurück zum Zitat Pickens CL, Milliron AR, Fussner AL, Dversdall BC, Langenstroer P, Ferguson S et al (1999) Abuse of guaifenesin-containing medications generates an excess of a carboxylate salt of beta-(2-methoxyphenoxy)-lactic acid, a guaifenesin metabolite, and results in urolithiasis. Urology 54:23–27CrossRef Pickens CL, Milliron AR, Fussner AL, Dversdall BC, Langenstroer P, Ferguson S et al (1999) Abuse of guaifenesin-containing medications generates an excess of a carboxylate salt of beta-(2-methoxyphenoxy)-lactic acid, a guaifenesin metabolite, and results in urolithiasis. Urology 54:23–27CrossRef
9.
Zurück zum Zitat van de Wetering-Krebbers SF, Jacobs PL, Kemperman GJ, Spaans E, Peeters PA, Delbressine LP et al (2011) Metabolism and excretion of asenapine in healthy male subjects. Drug Metab Dispos 39:580–590CrossRef van de Wetering-Krebbers SF, Jacobs PL, Kemperman GJ, Spaans E, Peeters PA, Delbressine LP et al (2011) Metabolism and excretion of asenapine in healthy male subjects. Drug Metab Dispos 39:580–590CrossRef
10.
Zurück zum Zitat Wojcikowski J, Danek PJ, Basinska-Ziobron A, Puklo R, Daniel WA (2020) In vitro inhibition of human cytochrome P450 enzymes by the novel atypical antipsychotic drug asenapine: a prediction of possible drug-drug interactions. Pharmacol Rep 72:612–621CrossRef Wojcikowski J, Danek PJ, Basinska-Ziobron A, Puklo R, Daniel WA (2020) In vitro inhibition of human cytochrome P450 enzymes by the novel atypical antipsychotic drug asenapine: a prediction of possible drug-drug interactions. Pharmacol Rep 72:612–621CrossRef
Metadaten
Titel
Solving an unusual case of acute kidney injury: Answers
verfasst von
Uttam Garg
Eugenio Taboada
Katherine L. Kurzinski
Clarence C. Frazee
Darcy K. Weidemann
Tarak Srivastava
Publikationsdatum
04.10.2021
Verlag
Springer Berlin Heidelberg
Erschienen in
Pediatric Nephrology / Ausgabe 12/2021
Print ISSN: 0931-041X
Elektronische ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-021-05263-w

Weitere Artikel der Ausgabe 12/2021

Pediatric Nephrology 12/2021 Zur Ausgabe

ADHS-Medikation erhöht das kardiovaskuläre Risiko

16.05.2024 Herzinsuffizienz Nachrichten

Erwachsene, die Medikamente gegen das Aufmerksamkeitsdefizit-Hyperaktivitätssyndrom einnehmen, laufen offenbar erhöhte Gefahr, an Herzschwäche zu erkranken oder einen Schlaganfall zu erleiden. Es scheint eine Dosis-Wirkungs-Beziehung zu bestehen.

Erstmanifestation eines Diabetes-Typ-1 bei Kindern: Ein Notfall!

16.05.2024 DDG-Jahrestagung 2024 Kongressbericht

Manifestiert sich ein Typ-1-Diabetes bei Kindern, ist das ein Notfall – ebenso wie eine diabetische Ketoazidose. Die Grundsäulen der Therapie bestehen aus Rehydratation, Insulin und Kaliumgabe. Insulin ist das Medikament der Wahl zur Behandlung der Ketoazidose.

Frühe Hypertonie erhöht späteres kardiovaskuläres Risiko

Wie wichtig es ist, pädiatrische Patienten auf Bluthochdruck zu screenen, zeigt eine kanadische Studie: Hypertone Druckwerte in Kindheit und Jugend steigern das Risiko für spätere kardiovaskuläre Komplikationen.

Betalaktam-Allergie: praxisnahes Vorgehen beim Delabeling

16.05.2024 Pädiatrische Allergologie Nachrichten

Die große Mehrheit der vermeintlichen Penicillinallergien sind keine. Da das „Etikett“ Betalaktam-Allergie oft schon in der Kindheit erworben wird, kann ein frühzeitiges Delabeling lebenslange Vorteile bringen. Ein Team von Pädiaterinnen und Pädiatern aus Kanada stellt vor, wie sie dabei vorgehen.

Update Pädiatrie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.