Neurotoxicity and nephrotoxicity caused by combined use of lithium and risperidone: a case report and literature review
© The Author(s). 2016
Received: 5 August 2016
Accepted: 27 October 2016
Published: 14 December 2016
Combination lithium, a mood stabilizer, and risperidone, an atypical antipsychotic drug, is widely used for treatment of psychotic disorders. Rare reports concern severe adverse drug reaction in multiple organic systems with their combined use. We report two episodes of neurotoxicity and nephrotoxicity in a patient following the combined use of lithium and risperidone.
A 55-year-old male had a diagnosis of schizoaffective disorder at the age of 51. He was initially treated with a combination of lithium and olanzapine 5 to 15 mg/day for 2 years. He was admitted to psychiatric ward at the age of 53 due to manic episode with psychotic feature. Because of poor blood sugar control, we switched olanzapine 20 mg/day to risperidone 4.5 mg/day with combination of lithium 900mg/day. The patient presented neurotoxicity, neuroleptic-malignant-syndrome like symptoms, and nephrotoxicity, elevation of blood creatinine and decreased urine output few days later. These signs were fully recovered within 2 days after we discontinued all medications and gave normal saline hydration. Then we re-administered decreased dosage of lithium 600 mg/day and risperidone 3 mg/day, and the similar episode occurred again 3 days later. All drugs were discontinued again, then his delirium resolved and abnormal data returned to normal 1 day later. Finally, the patient was treated with risperidone 2 mg/day as monotherapy, and no episode of neurotoxicity and nephrotoxicity appeared in the following 2 years.
The case exemplifies neurotoxicity and nephrotoxicity after combined use of lithium and risperidone. These adverse effects resolved soon after discontinuing these medications and adequate hydration. Clinicians should be cautious about neurological and renal adverse effects.
KeywordsRisperidone Lithium Neurotoxicity Acute kidney injury Drug-drug interaction
Seven previous reports and 2 episodes of neurotoxicity and nephrotoxicity in our patient caused by combined use of lithium and risperidone
Risperidone dose (mg)
Lithium dose (mg)
Time to onseta
Laboratory values and Image
Cr: NA; Li: 1.36
Cr: 1.6; Li: 0.6; CPK: 1428
Cr: NA; Li: 0.7; CPK: 791
EEG: Abnormal; CK: 953
EEG: Abnormal; Cr: NA; Li: 1.47
EEG: Abnormal; CPK: 953
BUN/Cr: 24/1.33; Li: 1.42; CK: 975
BUN/Cr: 29/1.36; Li: 1.54; CK: 90
A 55-year-old male had a diagnosis of schizoaffective disorder at the age of 51. He was initially diagnosed with bipolar I disorder at the age of 30, and mainly treated with a combination of lithium and valproic acid from age 30 to 51. At the age of 51, he was observed to have a manic episode concurrent with persecutory delusions and auditory hallucination. These psychotic symptoms persisted for more than 3 weeks after his manic symptoms had subsided. Later, a combination of lithium and olanzapine 5 to 15 mg/day were given as the main treatment. In addition, he had history of type 2 diabetes mellitus and hyperlipidemia for more than 10 years. He did not have any substance use or neurological disorder before. This time, after poor drug adherence for 4 months, he was admitted to our ward at the age of 53, due to symptoms including elevated mood, increased goal-directed activity, talkativeness, decreased need for sleep, and grandiose delusion lasting for 1 week.
Lithium 600 mg/day and olanzapine 10 mg/day were initially prescribed, and the dosages were titrated to 900 mg/day and 20 mg/day, respectively, over 1 week. His lithium serum level was reported to be 0.60 mEq/L (day 4) and 0.58 mEq/L (day 14). Because of poor blood sugar control, intramuscular injection of risperidone 25 mg was prescribed for switching antipsychotic agent on day 15. Olanzapine was discontinued and risperidone 4.5 mg/day was started on days 22 to 24. However, on day 27, the patient presented slurred speech, muscle rigidity, delirium (confused consciousness, inattention, and disorientation), and decreased urine output. At the same time, he did not present fever, focal neurological signs, or gastrointestinal symptoms. Laboratory data showed: blood urea nitrogen (BUN; 24 mg/dL), creatinine (1.33 mg/dL), serum lithium (1.42 mEq/L) on day 28, and creatine kinase (975 U/L) on day 29, compared with BUN (8 mg/dL) and creatinine (0.8 mg/dL) on admission. All medications were discontinued and he was treated with normal saline hydration. The delirium and abnormal laboratory data were fully recovered within 2 days, as follows: BUN (12 mg/dL), creatinine (0.82 mg/dL), and serum lithium (0.82 mEq/L). Lithium 600 mg/day and risperidone 3 mg/day were re-administered on day 32. But symptoms of delirium and elevated BUN (29 mg/dL), creatinine (1.36 mg/dL), serum lithium (1.54 mEq/L), and creatine kinase (90 U/L) were noted on day 35. All drugs were discontinued again and fluid hydration was given. One day later, the delirium resolved and abnormal data returned to normal: BUN (16 mg/dL), creatinine (0.88 mg/dL), and serum lithium (1.06 mEq/L). Finally, risperidone 2 mg/day monotherapy was given on day 38. The patient was discharged in a stable condition on day 42. He was kept regular treatment with risperidone 2 to 3 mg/day, and no episode of neurotoxicity and nephrotoxicity appeared in the following 2 years.
Our patient had 2 episodes of neurotoxicity and nephrotoxicity during this hospitalization. He presented delirium, acute kidney injury (AKI) with increased level of serum creatinine , and lithium intoxication, which had developed soon after combined administration of lithium and risperidone, and subsided after discontinuing these medications. There were no other obvious medical causes that could better account for the development of above symptoms in this patient. The switching of antipsychotics was suitable for our patient with history of type 2 diabetes mellitus and hyperlipidemia . His clinical features were considered to be side effects of lithium-risperidone interaction. The rating on the Naranjo Adverse Drug Reaction Probability Scale was 10, considered a “definite” adverse effect .
We searched PubMed from inception to June 2016 for literature review of neurotoxicity and nephrotoxicity due to combined use of lithium and risperidone. Google Scholar and pharmacovigilance databases of UK, Dutch, Australian, and Canadian were also searched for additional relevant articles. The search terms were: “lithium” and “risperidone” and (neuroto* or nms or neuroleptic malignant syndrome or delirium) as Search 1; lithium and risperidone and (nephroto* or renal failure or kidney injury) as Search 2. Articles without the direct concomitant use of lithium and risperidone or with toxicity highly related to other physical problem or obscure support were excluded. The Search 1 and 2 finally yielded 7 articles (twenty results from PubMed, then 14 articles were excluded and 1 report were included from Google Scholar) and showed in Table 1 [3–9]. These cases showed the mean age of 56.3 years, and no gender difference (4 females). The doses of lithium and risperidone ranged from 450 to 1500 mg/day and 2 to 6 mg/day, respectively, which are within normal therapeutic range. Side effects were noted within 3 weeks (5 of 7 cases) after the initial combination of lithium and risperidone, and varied from 4 days to 2 years. All cases developed neurotoxicity with symptoms of lethargy, delirium, and even neuroleptic malignant syndrome (NMS) (4 of 7 cases). NMS is characterized by delirium, muscular rigidity, fever, and autonomic nervous system dysregulation with typically high levels of creatine phosphokinase but not necessary in elevation of creatinine [13, 14]. Furthermore, our report specially showed the change of renal function in detail compared to previous reports.
There are two hypotheses of neurotoxicity from drug-drug interaction between lithium and risperidone. One is pure lithium intoxication-induced neurotoxicity without a relationship with risperidone . The other one is that both lithium and risperidone increase the dopamine receptor blockade. Lithium inhibits pre-synaptic dopamine release, and risperidone blocks dopamine receptors . As for nephrotoxicity, there are inconsistent results. One study including 13 patients indicates that switching a combination of lithium plus a conventional antipsychotic to a combination of lithium plus risperidone within 9 days is generally well tolerated and no statistically significant differences in the pharmacokinetics of serum lithium . The other studies support lithium and risperidone may each induce it. Lithium may impair tubular function and next result in several renal complications, including AKI [16, 17]. Risperidone was also described as increasing the risk of AKI in a population-based cohort study . Our case is an indicator to prove the nephrotoxicity by the concomitant use of these pharmaceuticals. He did not have a history of AKI while being treated with lithium or risperidone alone. We assume his AKI have a “2-pronged” effect of nephrotoxicity, which causes functional impairment of nephrons.
Based on the literature review and our report, close observation of neurological signs for at least 3 weeks is necessary when lithium and risperidone are used at the same time. Once neurotoxicity occurs, further monitoring of renal function for nephrotoxicity survey is also required. Discontinuance of these agents will lead to remission of the aforementioned adverse effects.
Blood urea nitrogen
Neuroleptic malignant syndrome
Authors thanks the patient to agree for publication of this report.
This report received no research funding.
Availability of data and materials
Dr. Hsu CW wrote the first draft. Drs. Lee Y and Lee CY helped with discussion. Drs. Hsu CW, Lee Y, Lee CY, and Lin PY gave critical comments on revision. Drs. Hsu CW and Lin PY finalized the manuscript. All the authors read and approved the final manuscript.
Chih-Wei Hsu, M.D., Yu Lee, M.D., M.M.S., Chun-Yi Lee, M.D., M.S., Pao-Yen Lin, M.D., Ph.D.*
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The case described in this report has signed the informed consent for publication.
There is no competing conflict of interests regarding publication of this paper.
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