Cardiac arrest in a healthy young adult after kratom tea
35M had out-of-hospital arrest with no co-ingestants; transient LV systolic dysfunction and small hypoxic infarcts; ultimately recovered.
Peer-reviewed, real-world cases linked to Mitragyna speciosa (kratom). Each card contains a plain-English summary and a direct PDF link. Educational use only — not medical advice.
35M had out-of-hospital arrest with no co-ingestants; transient LV systolic dysfunction and small hypoxic infarcts; ultimately recovered.
44M suffered out-of-hospital VF arrest; ECG showed prolonged QT. Cath and MRI were normal; he received a subcutaneous ICD. Authors warn of potential proarrhythmic risk (especially with stimulants/caffeine).
18M collapsed in training with ventricular fibrillation; plasma mitragynine 98 ng/mL and caffeine present. Normal echo/CTA/CMR; ICD implanted for secondary prevention. Authors implicate synergy of kratom, energy drink, and exertion; caution against stimulant combinations.
25M ingesting ~84–100 g/day kratom presented with seizure-like syncope; ECG showed type-1 Brugada pattern (QRS 160 ms, QTc 654 ms) that normalized after abstinence and electrolyte repletion.
26-year-old male suffered cardiac arrest ~24 h after kratom ingestion. Temporary response to IV lipid emulsion (“lipid rescue”) before multi-organ failure. Authors propose cardiotoxic metabolites and discuss emergency treatment options.
32-year-old man with acute jaundice and cholestatic hepatitis after heavy kratom use. Viral, autoimmune, and metabolic causes excluded. Liver enzymes improved after discontinuation. Authors highlight kratom’s potential hepatotoxicity and misuse amid the opioid crisis.
38-year-old man with dark urine and pruritus after kratom ingestion. Biopsy showed portal inflammation with eosinophils, bile duct damage, and canalicular cholestasis. First report detailing histopathology of kratom-induced liver injury.
37F developed severe cholestatic hepatitis that histologically mimicked PBC; autoimmune markers negative. Improved rapidly after stopping kratom.
52M developed bilirubin 28.9 mg/dL after ~2 months of daily kratom. Biopsy: canalicular cholestasis & bile-duct injury. Improved with UDCA + cessation.
47M developed mixed pattern DILI ~21 days after starting kratom; recurrence within 2 days on rechallenge confirmed causality (RUCAM high probability).
47M with jaundice/pruritus after 3 weeks of kratom; cholestatic pattern, improving off-product. Paper reviews rising DILI from herbal products and shows current U.S. patchwork legality.
23M developed bilirubin 34 mg/dL and ALP 220 IU/L after 14 days of high-dose kratom (30 g/day). Biopsy: canalicular cholestasis, perivenular necrosis, mixed portal inflammation.
56M with cholestatic liver failure after kratom; Tbili peaked at 70.6 mg/dL. Four therapeutic plasma exchanges rapidly reduced bilirubin and improved clinical status.
64M experienced generalized seizure and coma after kratom–Datura tea; first lab-confirmed seizure case; neuroexcitation suspected.
20s M with heavy kratom use; bilateral cytotoxic edema on DWI/ADC reversed at 2 months; suggests transient vasospasm/vasculitis.
39F sudden whole-body paralysis ~1h post-ingestion with intact awareness; workup negative; neuromuscular blockade mechanism proposed.
35M with schizoaffective disorder presented with new paranoid delusions after escalating kratom use; symptoms persistent despite trials; stimulant-like effects suspected.
63M long-term daily use “failed” under stress; detox and switch to standard pharmacotherapy/psychotherapy; functional dependence without clear withdrawal.
31M substance-induced psychosis after cannabinoids + kratom; self-amputation; stabilized on antipsychotics; later reconstruction after abstinence.
Term infant developed withdrawal (Finnegan >10) despite negative opioid tox screen; oral morphine taper. Screen for kratom in NAS workups.
Postpartum mother using large daily kratom doses developed dependency; newborn required NICU morphine; placental transfer documented.
Term infant Finnegan 18; required oral morphine for ~2 months; emphasizes detailed maternal supplement history.
32M with blue-gray facial/neck hyperpigmentation after long-term kratom; biopsy: melanin-laden histiocytes; fades after cessation.
Two cases; 730 nm picosecond titanium-sapphire laser achieved >90% clearance without recurrence.
56F with postmortem mitragynine 2,500 ng/mL — independently lethal; demonstrates kratom-only lethality at high dose.
15F ingested ~225 g capsules; nausea, tremor, hypokalemia, QTc 474 ms; resolved in ~14 h with supportive care.
18M in shock with PCT >200 ng/mL; cultures negative; improved with pressors — overdose/tox effect suspected.
35M apneic with mixed shock; RSI, dual pressors, hemodialysis; extubated and discharged after 72 h.
26M with flubromazolam/clonazolam overdose, CK 131,920 U/L and AKI; kratom present among belongings.
37F dependent on kratom extract; severe opioid-like withdrawal; clonidine/hydroxyzine effective.
72M developed in-hospital kratom withdrawal; controlled with buprenorphine-naloxone 8/2 mg daily; interaction cautions noted.
38M chronic kratom user with marked transaminitis; experienced classic precipitated withdrawal after IM naltrexone. Consider test dosing.
37M on amitriptyline developed anticholinergic effects and mild transaminitis while using kratom; improved after stopping kratom; CYP2D6 inhibition suspected.
Early-40s F developed SS two days after starting Paxlovid while on buspirone, quetiapine, and daily kratom; improved with lorazepam. Highlights ritonavir CYP3A inhibition.
56M started oral naltrexone 50 mg; acute agitation/hallucinations; required dexmedetomidine and IV benzodiazepines. Screen for kratom prior to antagonists.
61M persistent K⁺ > 5.5 mmol/L; normalized after stopping kratom. First reported kratom-induced hyperkalemia.
62M presented with Na⁺ 103 mEq/L; controlled saline correction + cessation; mechanism likely ADH/κ-receptor effects.
54M switched products, developed large ICH; product contained ~15% PEA — not listed on label. Illustrates risk of adulterants.