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GGZ Delfland locatie St Jorisweg 2, 2612 GA, Delft, The Netherlands
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Abstract |
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To report the management of three cases of clozapine-induced enuresis, by description of these cases and literature review.
RESULTS
Heavy sedation, generalised epilepsy and diabetes mellitus induced by clozapine are some of the mechanisms that underlie the emergence of this side-effect.
CLINICAL IMPLICATIONS
These cases illustrate several different pathophysiological mechanisms necessitating further diagnostic investigations before adequate treatment can be started. Clozapine-induced enuresis is probably under-reported owing to the embarrassing nature of this side-effect.
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Introduction |
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The pathophysiological mechanism of clozapine-induced enuresis remains unclear. It is suggested that sedation prevents the patients from waking up during sleep to empty the bladder, especially if combined with other sedative medication (Steingard, 1994). Others suggest that clozapine is a potent anticholinergic antagonist, which can lead to urinary retention and subsequent overflow incontinence (Aronowitz et al, 1995).
Warner et al (1994) report the occurrence of clozapine-induced enuresis in five out of 12 patients in the first 3 months of treatment resolving spontaneously in all cases. Centorrino et al (1994), however, report enuresis as a late side-effect, which is not correlated to the plasma level of the drug.
In these case reports we suggest a systematic treatment approach, as the pathophysiology of this side-effect appears to be diverse.
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Case reports |
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Patient B, a 27-year-old male suffering from schizophrenia, was seen for complaints of bedwetting. He was also known to have lost consciousness twice in the day time, without tongue biting or incontinence. The patient was on clozapine 400 mg once daily and lactulose 30 ml once daily. The electroencephalogram recording showed signs of a generalised epilepsy. After clozapine was replaced by olanzapine the patient experienced a relapse of his psychosis. Because his psychosis was known to be resistant to classic neuroleptic medication, clozapine 400 mg once daily was restarted, with a plasma level of 0.59 mg/l, and the olanzapine stopped. Valproic acid 500 mg three times a day was added to prevent a recurrence of seizures. His psychosis remitted and he had no further episodes of enuresis or seizures.
Patient C, a 29-year-old male suffering from schizophrenia, was seen for nocturnal enuresis. At previous investigations serum glucose levels were within the normal range. He was on clozapine 200 mg twice daily (unknown plasma level), fluvoxamine 50 mg twice daily and oxazepam 25 mg twice daily. When he was seen for his nocturnal enuresis the urine sample taken was positive for glucose, with serum glucose levels of 23.4 and 23.8 mmol/l and a glycosolated haemoglobin of 8.4%. After insulin therapy was started the nocturnal enuresis remitted. High doses of insulin were necessary to control the diabetes. Two years later clozapine was stopped owing to high fever and an infiltration in the left middle lung. Zuclopenthixol was initiated. After the switch of the antipsychotic medication the dose of insulin was decreased and after a few months it was stopped as the diabetes remitted.
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Discussion |
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Patients can have a recurrence of enuresis with a history of prior enuresis (Berrios, 1986). Enuresis occurring after initiation of clozapine can be attributed to the medication. Reducing sedative co-medication as well as clozapine prevents the patient from sleeping through his or her urge to void the bladder in his or her sleep, as seen in case A.
A spontaneous remission of this side-effect is possible (Warner et al, 1994). Epileptic seizures can present as nocturnal enuresis as shown in case B. During the first 6 months after marketing, 71 out of 5629 patients (1.3%) using clozapine were shown to have had generalised tonicclonic seizures (Pacia & Devinsky, 1994). Patients with a history of seizures or epilepsy were more likely to have seizures soon after initiation of therapy. Seizures tended to occur at low doses (300 mg/day) during the titration phase and at high doses (600 mg/day) during the maintenance phase. The majority of patients who had seizures were able to continue the medication with dose reduction and more gradual dose titrating, or with the addition of anticonvulsive medication.
Recently, clozapine has been associated with the occurrence of diabetes mellitus (Wirshing et al, 1998). Fifteen cases have so far been described (Brugman et al, 2000). A positive family history of diabetes and a personal history of impaired glucose tolerance may increase the risk of developing this side-effect. Treatment of the diabetes can alleviate this indirectly caused clozapine-induced enuresis, as shown in case C.
Treatment with desmopressin (a synthetic analogue of the antidiuretic hormone vasopressin), 10 µg in each nostril at bedtime, has been suggested (Steingard, 1994; Aronowitz et al, 1995; Frankenbur et al, 1996). It decreases the formation of urine by increasing water reabsorption by the renal collecting ducts. Others have suggested the use of oxybutynin (Frankenburg et al, 1996) and trihexyphenidyl (Poyurovski et al, 1996) to treat clozapine-induced enuresis.
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Conclusion |
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References |
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ARONOWITZ, J. S., SAFFERMAN, A. Z. & LIEBERMAN, J. A. (1995) Management of clozapine-induced enuresis. American Journal of Psychiatry, 152, 472-473.
BERRIOS, G. E. (1986) Temporary urinary incontinence
in the acute psychiatric patient without delirium or dementia.
British Journal of Psychiatry,
149,
224-227.
BRUGMAN, N. J., COHEN, D. & DE VRIES, R. H. (2000) Diabetes mellitus after treatment with clozapine. Nederlands Tijdschrift voor Geneeskunde, 144, 437-439.[Medline]
CENTORRINO, F., BALDESSARINI, R. J., KANDO, J. C., et al (1994) Clozapine and metabolites: concentration in serum and clinical findings during treatment of chronically psychotic patients. Journal of Clinical Psychopharmacology, 14, 119-125.[Medline]
FRANKENBURG, F. R., KANDO, J. C., CENTORRINO, F., et al (1996) Bladder dysfunction associated with clozapine therapy. Journal of Clinical Psychiatry, 57, 39-40.
KANE, J., HONIGFELD, G., SINGER, J., et al (1988) Clozaril collaborative group: clozapine for treatment-resistant schizophrenia: a double-blind comparison with chlorpromazine. Archives of General Psychiatry, 45, 789-796.[Abstract]
KRONIG, M. H., MUNNE, R. A., SZYMANSKI, S., et al
(1995) Plasma clozapine levels and therapeutic response for
treatment-refractory in schizophrenic patients. American Journal of
Psychiatry, 152,
179-182.
PACIA, S. V. & DEVINSKY, O. (1994)
Clozapine-related seizures: experience with 5629 patients.
Neurology, 44,
2247-2249.
POYUROVSKI, M., MODAI, I. & WEIZMAN, A. (1996) Trihexyphenidyl as a possible therapeutic option in clozapine-induced nocturnal enuresis. International Clinical Psychopharmacology, 11, 61-63.
STEINGARD, S. (1994) Use of desmopressin to treat clozapine-induced nocturnal enuresis. Journal of Clinical Psychiatry, 55, 315-316.[Medline]
WARNER, J. P., HARVEY, C. A. & BARNES, T. R. E. (1994) Clozapine and urinary incontinence. International Clinical Psychopharmacology, 9, 207-209.[Medline]
WIRSHING, D. A., SPELLBERG, B. J., ERHART, S. M., et al (1998) Novel antipsychotics and new onset diabetes. Biological Psychiatry, 44, 778-783.[CrossRef][Medline]
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