trimipramine

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Trimipramine Neuroleptic mal i gnant syndrome: 00 case report A 47-year-old woman with a 7 -year history of obsessive compulsive disorders and major depressi on had been previously treated with amitriptyline, thiothi xene , haloperidol , amoxapine and clomipramine wi thout success. Concu rr en t medications we re wa rfar in , for mitral valve replacement surgery 4 yea rs previously, estrogen/ progesterone combination since a hysterectomy 9 ye ars previously, and alprazolam 3 mg/day for an xiety . Following ECT therapy for a psychotic depressive episode whilst on clomipramine, treatment with trimipramine was initiated and within 2 weeks a dose of 250 mg/day had been reached . After 1 month of treatment it was noted that the patient had increased her fluid intake and was urinating more frequently. Muscular hypertonicity, pol yu ria and diarrhoea had developed a day after the last dose increase. She was admitted with extreme lead-pipe rigidity without cog-wheeling and was mute and unresponsive but awake with open eyes. She had grossly elevated levels of creat ini ne phosphokinase and white blood cells and a low sodium leve l. IV fluids were administered to compensate for the high urine output, and over 3 days electrolyte and renal function values normalised. About 24 hours after admission she developed bilateral aspiration pneumonia which was treated with IV antibacterials. Urine sample analysis showed only tricyclic metabolites and no neuroleptics. IV dantrolene 50 mg/6 hours and oral bromocriptine 2.5 mg/6 hours were administered for 3 days over a general improvement in muscular rigidity, alertness and fever seen within the following 2 weeks. Clomipramine and lithium treatment were initiated after recovery from pneumonia and substantial improvement was seen over the next 4 months. Langlow JR. Alarcon RD T"mlpramlne-Induced neuroleptic malignant syndrome after transient psychogenic polydipsia In one patient Journal of Clinical Psychiatry 50 144· 145, Apr 1989 ....

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Trimipramine Neuroleptic malignant syndrome: 00 case report

A 47-year-old woman with a 7 -year history of obsessive compulsive disorders and major depression had been previously treated with amitriptyline, thiothixene, haloperidol , amoxapine and clomipramine wi thout success. Concurren t medications were warfar in , for mitral valve replacement surgery 4 years previously, estrogen/ progesterone combination since a hysterectomy 9 years previously, and alprazolam 3 mg/day for anxiety . Following ECT therapy for a psychotic depressive episode whilst on clomipramine, treatment with trimipramine was initiated and within 2 weeks a dose of 250 mg/ day had been reached .

After 1 month of treatment it was noted that the patient had increased her fluid intake and was urinating more frequently . Muscular hypertonicity, polyu ria and diarrhoea had developed a day after the last dose increase . She was admitted with extreme lead-pipe rigidity without cog -wheeling and was mute and unresponsive but awake with open eyes. She had grossly elevated levels of creatinine phosphokinase and white blood cells and a low sodium level. IV fluids were administered to compensate for the high urine output , and over 3 days electrolyte and renal function values normalised . About 24 hours after admission she developed bilateral aspiration pneumonia which was treated with IV antibacterials. Urine sample analysis showed only tricyclic metabolites and no neuroleptics. IV dantrolene 50 mg/6 hours and oral bromocriptine 2.5 mg/6 hours were administered for 3 days over a general improvement in muscular rig idity, alertness and fever seen within the following 2 weeks. Clomipramine and lithium treatment were initiated after recovery from pneumonia and substantial improvement was seen over the next 4 months.

Langlow JR. Alarcon RD T"mlpramlne-Induced neuroleptic malignant syndrome after transient psychogenic polydipsia In one patient Journal of Clinical Psychiatry 50 144·145, Apr 1989 ....