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The Serotonin Syndrome Hunter Area Toxicology Service Serotonin 5–hydroxytryptamine or 5–HT Discovered in 1948 Major role in multiple states – aggression, pain, sleep, appetite – anxiety, depression – migraine, emesis Hunter Area Toxicology Service Serotonin metabolism Dietary tryptophan – converted to 5–hydroxy– tryptophan by tryptophan hydroxylase – then to 5-HT by a non–specific decarboxylase Specific transport system into cells Degradation – mainly monoamine oxidase (MAO–A > MAO–B) – 5–hydroxyindoleacetic acid (5-HIAA) in urine Hunter Area Toxicology Service Serotonin actions Serotonin causes the following effects – excitation/inhibition of CNS neurons – stimulation of peripheral nociceptive nerve endings – vascular effects constriction (direct and via sympathetic innervation) dilatation (endothelium dependent) platelet aggregation increased microvascular permeability Hunter Area Toxicology Service Serotonin actions – increased gastrointestinal motility direct excitation of smooth muscle and indirect action via enteric neurons – contraction of other smooth muscle eg bronchi, uterus Hunter Area Toxicology Service Serotonin roles Peripheral – – – – – – peristalsis vomiting platelet aggregation and haemostasis inflammatory mediator sensitisation of nociceptors microvascular control Hunter Area Toxicology Service Serotonin roles Central – – – – – – – control of appetite sleep mood hallucinations stereotyped behaviour pain perception vomiting Hunter Area Toxicology Service Serotonin receptors 5–HT1 – – – – – 7 trans–membrane domains G protein linked cAMP dependant anxiolytic and antidepressant subtypes 5–HT1A, 5–HT1B, 5–HT1D, 5–HT1E, 5–HT1F Hunter Area Toxicology Service 5–HT1 5–HT1A – limbic system regulation of emotions – neocortex – hypothalamus – substantia gelatinosa proprioception 5–HT1B (rat) Hunter Area Toxicology Service 5–HT1 5–HT1D – autoreceptors inhibitory feedback – heteroreceptors modulate release – acetylcholine – glutamate – anti–migraine effect of sumatriptan Hunter Area Toxicology Service 5–HT1 5–HT1E – ? functional role 5–HT1F – – – – ? functional role distribution includes CNS, uterus, mesentery inhibit cAMP high affinity sumatriptan, methysergide Hunter Area Toxicology Service Serotonin receptors 5–HT2 – – – – – 7 trans–membrane domains G protein linked phospholipase C dependant hallucinogens subtypes 5–HT2A, 5–HT2B, 5–HT2C Hunter Area Toxicology Service 5–HT2 5–HT2A – Periphery contraction of vascular/non–vascular smooth muscle platelet aggregation increased capillary permeability modulation of the release of other neurotransmitters and hormones – ACh, adrenaline, dopamine, excitatory amino acids, vasopressin Hunter Area Toxicology Service 5–HT2 5–HT2A – CNS motor behaviour head twitch wet dog shakes sleep regulation nociception neuroexcitation Hunter Area Toxicology Service 5–HT2 5–HT2B (rat) – stomach fundus 5–HT2C – – – – – CSF production locomotion eating disorders anxiety migraine Hunter Area Toxicology Service Serotonin receptors 5–HT3 – ligand gated cation channels 5-HT4 (rat) – coupled to adenylate cyclase 5-HT5 (rat) – coupled to adenylate cyclase – subtypes 5–HT5A, 5–HT5B Hunter Area Toxicology Service 5–HT3 Peripheral – located exclusively on neurons and mediate neurotransmitter release - parasympathetic, sympathetic, sensory and enteric – cardiac inhibition/activation, pain, initiation of the vomiting reflex Central – facilitate dopamine and 5–HT release, inhibit ACh and noradrenaline release – anxiety, depression, memory, tolerance and dependence Hunter Area Toxicology Service Serotonin receptors 5-HT6 (rat) 5-HT7 (rat and human) – coupled to adenylate cyclase – significance unknown Hunter Area Toxicology Service Serotonin excess Oates (1960) suggested excess serotonin as the cause of symptoms after MAOIs with tryptophan Animal work (1980s) attributed MAOI/pethidine interaction to excess serotonin Insel (1982) often quoted as describing the serotonin syndrome Sternbach (1991) developed diagnostic criteria for serotonin syndrome Hunter Area Toxicology Service Sternbach criteria Mental status changes (confusion, hypomania) Agitation Myoclonus Hyperreflexia Diaphoresis Shivering Tremor Diarrhoea Incoordination Fever Hunter Area Toxicology Service Diarrhoea Serotinergic drugs Serotonin precursors – – – – S–adenyl–L–methionine L–tryptophan 5–hydroxytryptophan dopamine Hunter Area Toxicology Service Serotinergic drugs Serotonin re–uptake inhibitors – citalopram, fluoxetine, fluvoxamine, paroxetine, sertraline, venlafaxine – clomipramine, imipramine – nefazodone, trazodone – chlorpheniramine – cocaine, dextromethorphan, pentazocine, pethidine Hunter Area Toxicology Service Serotinergic drugs Serotonin agonists – – – – – fenfluramine, p–chloramphetamine bromocriptine, dihydroergotamine, gepirone sumatriptan buspirone, ipsapirone eltoprazin, quipazine Hunter Area Toxicology Service Serotinergic drugs Monoamine oxidase inhibitors (MAOIs) – clorgyline, isocarboxazid, nialamide, pargyline, phenelzine, tranylcypromine – selegiline – furazolidone – procarbazine Hunter Area Toxicology Service Serotinergic drugs Reversible inhibitors of MAO (RIMAs) – brofaramine – befloxatone, toloxatone – moclobemide Hunter Area Toxicology Service Serotinergic drugs Miscellaneous/mixed – lithium – lysergic acid diethylamide (LSD) – 3,4–methylenedioxymethamphetamine (MDMA, ecstasy), methylenedioxyethamphetamine (eve) – propranolol, pindolol Hunter Area Toxicology Service Incidence Over last 10 years 4130 admissions for deliberate self poisoning 267 admissions for serotinergic drug overdose 41 admissions with serotonin syndrome Hunter Area Toxicology Service Incidence Serotinergic drug Serotonin syndrome 20 Percent 15 10 5 0 87 88 Hunter Area Toxicology Service 89 90 91 92 93 94 95 96 97 Serotinergic drugs taken Paroxetine Moclobemide Sertraline Fluoxetine Clomipramine Phenelzine Lithium Tranylcypromine Imipramine Hunter Area Toxicology Service All serotinergic drugs (n=267) Serotonin syndrome (n=41) 58 (22%) 56 (21%) 51 (19%) 43 (16%) 41 (15%) 14 (5%) 11 (4%) 7 (3%) 2 (1%) 11 (27%) 10 (24%) 15 (37%) 3 (7%) 1 (2%) 3 (7%) 1 (2%) 3 (7%) 2 (5%) Serotinergic drugs (Odds ratios) Single serotinergic drug Serotonin syndrome (n=41) No serotonin syndrome (n=226) Odds ratio (95% CI) Sertraline Paroxetine Moclobemide Fluoxetine Phenelzine Tranylcypromine Lithium Clomipramine Imipramine 11 (26.8%) 9 (22.0%) 6 (14.6%) 2 (4.9%) 2 (4.9%) 1 (2.4%) 1 (2.4%) 0 0 33 (14.6%) 44 (19.5%) 43 (19.0%) 38 (16.8%) 9 (4.0%) 3 (1.3%) 1 (0.4%) 39 (17.3%) 0 2.2 (0.98–4.7) 1.2 (0.5–2.6) 0.7 (0.3–1.9) 0.3 (0.1–1.1) 1.2 (0.3–6.0) 1.9 (0.2–18.4) 5.7 (0.3–92.2) 0.0 (0.0–0.4) Undefined Total 32 (78.0%) 210 (92.9%) – Hunter Area Toxicology Service Sternbach criteria (%) Sternbach (n=38) Confusion/hypomania Agitation Myoclonus Hyperreflexia Diaphoresis Shivering Tremor Diarrhoea Ataxia/incoordination Fever Hunter Area Toxicology Service 42 45 34 29 26 26 26 16 13 NR Sporer (n=79) 45 NR 43 47 31 21 NR 10 38 28 HATS (n=41) 42 76 12 81 10 15 44 15 15 44 Frequency of Sternbach criteria Patients (%) ) Serotinergic drug overdose with signs 45 40 35 30 25 20 15 10 5 0 0 1 Hunter Area Toxicology Service 2 3 4 5 6 7 8 9 10 Other clinical features (%) Inducible clonus Tachycardia Mydriasis Spontaneous clonus Hypertonia/rigidity Coma Ocular clonus/oscillations Nystagmus Rhabdomyolysis Akathisia Seizures Lacrimation Oculogyric crisis Opisthotonus Hunter Area Toxicology Service 56 51 39 29 24 20 20 12 5 2 2 0 0 0 Frequency of all clinical features Serotinergic drug overdose with signs 30 Patients (%) ) 25 20 15 10 Hunter Area Toxicology Service 24 22 20 18 16 14 12 10 8 6 4 2 0 0 5 Sternbach criteria in HATS (%) Serotonin syndrome (n=41) Hyperreflexia Agitation Fever Tremor Confusion/hypomania Diarrhoea Ataxia/incoordination Shivering Myoclonus Diaphoresis Hunter Area Toxicology Service 80.5 75.6 43.9 43.9 41.5 14.6 14.6 14.6 12.2 9.8 Serotinergic drug, Other drug no SS (n=226) (n=3863) 28.3 5.3 5.3 2.2 1.8 10.2 3.5 0.9 0.4 0.4 8.3 na 3.0 na 5.5 na na na 0.6 na Sternbach criteria (Odds ratio) Hyperreflexia Agitation Fever Tremor Confusion/hypomania Diarrhoea Ataxia/incoordination Shivering Myoclonus Diaphoresis Hunter Area Toxicology Service Serotonin syndrome vs no SS Serotinergic drug vs other drug 10.4 (4.6–23.8) 55.3 (22.0–138.7) 14.0 (6.0–32.6) 34.6 (11.7–101.9) 39.3 (12.2–126.4) 1.5 (0.6–4.2) 4.7 (1.5–14.3) 19.2 (3.7–99.0) 31.3 (3.5–275.4) 28.8 (3.1–264.4) 6.2 (4.7–8.2) na 2.9 (1.8–4.7) na 1.5 (0.9–2.3) na na na 3.8 (1.5–9.5) na Other clinical features in HATS (%) Inducible clonus Tachycardia Mydriasis Spontaneous clonus Hypertonia/rigidity Coma Ocular clonus/oscillations Nystagmus Rhabdomyolysis Akathisia Seizures Lacrimation Oculogyric crisis Opisthotonus Hunter Area Toxicology Service Serotonin syndrome (n=41) Serotinergic drug, no SS (n=226) Other drug (n=3863) 56.1 51.2 39.0 29.3 24.4 19.5 19.5 12.2 4.9 2.4 2.4 0 0 0 3.1 23.9 29.2 2.7 3.1 8.4 1.8 3.5 0 0.4 1.4 0 0.4 0 na 30.8 13.9 na 1.8 9.5 na 6.6 1.1 na 2.3 na na na Other clinical features (Odds ratio) Inducible clonus Tachycardia Mydriasis Spontaneous clonus Hypertonia/rigidity Coma Ocular clonus/oscillations Nystagmus Rhabdomyolysis Akathisia Seizures Lacrimation Oculogyric crisis Opisthotonus Hunter Area Toxicology Service Serotonin syndrome vs no SS Serotinergic drug vs other drug 40.0 (25.1–105.8) 3.3 (1.7–6.6) 1.6 (0.8–3.1) 15.7 (5.3–43.5) 10.1 (3.6–28.5) 2.6 (1.1–6.5) 13.5 (3.8–47.2) 3.8 (1.2–12.2) (1.6–) 5.6 (0.3–91.8) 1.9 (0.2–18.3) – – – na 0.9 (0.7–1.2) 2.7 (2.1–3.6) na 3.8 (2.2–6.6) 1.1 (0.7–1.6) na 0.7 (0.4–1.3) 0.7 (0.2–2.7) na 0.7 (0.2–1.8) na na na Major features Agitation Inducible clonus Confusion/hypomania Tremor Myoclonus Diaphoresis Shivering Spontaneous clonus Fever Ocular clonus/oscillations Hyperreflexia Hypertonia/rigidity Hunter Area Toxicology Service 55.3 (22.0–138.7) 40.0 (25.1–105.8) 39.3 (12.2–126.4) 34.6 (11.7–101.9) 31.3 (3.5–275.4) 28.8 (3.1–264.4) 19.2 (3.7–99.0) 15.7 (5.3–43.5) 14.0 (6.0–32.6) 13.5 (3.8–47.2) 10.4 (4.6–23.8) 10.1 (3.6–28.5) Minor features Ataxia/incoordination Nystagmus Tachycardia Coma Rhabdomyolysis Hunter Area Toxicology Service 4.7 (1.5–14.3) 3.8 (1.2–12.2) 3.3 (1.7–6.6) 2.6 (1.1–6.5) (1.6–) Non–features Akathisia Seizures Diarrhoea Mydriasis Lacrimation Oculogyric crisis Opisthotonus Hunter Area Toxicology Service 5.6 (0.3–91.8) 1.9 (0.2–18.3) 1.5 (0.6–4.2) 1.6 (0.8–3.1) – – – Suggested criteria Agitation/confusion/hypomania Clonus (inducible/spontaneous/ocular) Tremor/shivering/myoclonus Diaphoresis Fever Hyperreflexia Hypertonia/rigidity Hunter Area Toxicology Service Suggested criteria Serotinergic drug with serotonin syndrome Serotinergic drug without serotonin syndrome Patients (%) ) 60 50 40 30 20 10 0 0 Hunter Area Toxicology Service 1 2 3 4 5 6 7 Signs suggestive of serotinergic drug overdose Hyperreflexia Hypertonia/rigidity Myoclonus Fever Mydriasis Hunter Area Toxicology Service 6.2 (4.7–8.2) 3.8 (2.2–6.6) 3.8 (1.5–9.5) 2.9 (1.8–4.7) 2.7 (2.1–3.6) Treatment of serotonin syndrome Depends on severity Many (if not most) do not require treatment Many would benefit if a safe effective therapy was available Hunter Area Toxicology Service Severity of serotonin syndrome Mild – three symptoms are present but they are not progressive and not significantly affecting the patient – no action is required Moderate – four or more definite symptoms that between them cause significant impairment of functioning or distress to the patient – specific therapy may be indicated Hunter Area Toxicology Service Severity of serotonin syndrome Severe – most symptoms are present and significant impairment of consciousness or functioning is also present – often progression of symptoms, particularly fever – rapidly rising temperature (>39oC) is an indication for urgent intervention – specific therapy may be very beneficial Hunter Area Toxicology Service Drugs used to treat serotonin syndrome Non–specific blocking agents – methysergide – cyproheptadine –blockers – propranolol – pindolol Hunter Area Toxicology Service Drugs used to treat serotonin syndrome Benzodiazepines – lorazepam – diazepam – clonazepam Neuroleptics – chlorprothixene – chlorpromazine – haloperidol Hunter Area Toxicology Service Drugs used to treat serotonin syndrome Miscellaneous – chlormethiazole – nitroglycerine Drugs used for neuroleptic malignant syndrome – dantrolene – bromocriptine Hunter Area Toxicology Service 5–HT receptors in serotonin syndrome Originally thought to be 5–HT1 mediated (5–HT1A) – blocked in animals by non–specific 5–HT blockers methysergide cyproheptadine – not blocked by ketanserin (5–HT2 blocker) More recent evidence implicates 5–HT2 – failure of propranolol (5–HT1A blocker) in several cases – cyproheptadine more potent at 5–HT2 than 5–HT1 Hunter Area Toxicology Service Antagonist potencies Ki values (5–HT2) – chlorprothixene (0.43 nM) > chlorpromazine > cyproheptadine > haloperidol (36 nM) – limited experience suggests haloperidol ineffective Ki values (5–HT1) – chlorprothixene (230 nM) > haloperidol > chlorpromazine > cyproheptadine (3200 nM) Hunter Area Toxicology Service Therapy Moderate – when oral therapy suitable cyproheptadine 8 mg stat then 4 mg q4–6h – when oral therapy unsuitable or cyproheptadine fails chlorpromazine 50 mg IMI/IVI stat then up to 50 mg orally or IMI/IVI q6h Hunter Area Toxicology Service Therapy Severe – when symptoms are not progressive and fever < 39oC chlorpromazine 50–100 mg IMI/IVI stat then 50–100 mg orally or IMI/IVI q6h – when symptoms are progressive and fever < 39oC chlorpromazine 100–400 mg IMI/IVI over first two hours – when symptoms are progressive and fever > 39oC barbiturate anaesthesia, muscle relaxation ± active cooling chlorpromazine 100–400 mg IMI/IVI over first two hours Hunter Area Toxicology Service