Schizophrenia Research
Volume 115, Issue 2 , Pages 115-120, December 2009

Impact of real-world ziprasidone dosing on treatment discontinuation rates in patients with schizophrenia or bipolar disorder

  • Leslie Citrome

      Affiliations

    • Nathan S. Kline Institute for Psychiatric Research, Orangeburg, NY, USA
    • New York University School of Medicine, New York, NY, USA
    • Corresponding Author InformationCorresponding author. Nathan S. Kline Institute for Psychiatric Research, 140 Old Orangeburg Road, Orangeburg, NY 10962, USA. Tel.: +1 845 398 5595; fax: +1 845 398 5483.
  • ,
  • Christopher Reist

      Affiliations

    • University of California, Irvine, CA, USA
  • ,
  • Liisa Palmer

      Affiliations

    • Thomson Reuters, Ann Arbor, MI, USA
  • ,
  • Leslie B. Montejano

      Affiliations

    • Thomson Reuters, Ann Arbor, MI, USA
  • ,
  • Gregory Lenhart

      Affiliations

    • Thomson Reuters, Ann Arbor, MI, USA
  • ,
  • Brian Cuffel

      Affiliations

    • Pfizer Inc., New York, NY, USA
  • ,
  • James Harnett

      Affiliations

    • Pfizer Inc., New York, NY, USA
  • ,
  • Kafi N. Sanders

      Affiliations

    • Pfizer Inc., New York, NY, USA

Received 30 July 2009; received in revised form 12 September 2009; accepted 17 September 2009. published online 30 October 2009.

Abstract 

Background

The purpose of this study is to evaluate the relationship between maximum dose of ziprasidone and time to discontinuation in the treatment of schizophrenia/schizoaffective disorder and bipolar disorder in clinical practice.

Method

The 2001–2006 MarketScan Commercial and Medicare Databases were analyzed for maximum ziprasidone doses achieved in patients with schizophrenia/schizoaffective disorder or bipolar disorder. Ziprasidone maximum-dose groups were defined as low (20–60mg/d), medium (61–119mg/d), or high (120–160mg/d). Patients receiving >160mg/d were excluded. Mean time to discontinuation was evaluated across propensity score-matched dosing groups. Cox proportional hazard models were used to adjust for confounding when comparing the high- and medium-dose groups with the low-dose group.

Results

Data were available for 33,340 patients with schizophrenia/schizoaffective disorder, of whom 16.6% received low dose of ziprasidone, 22.0% medium dose, and 61.4% high dose. Of those subjects with bipolar disorder (n=27,751), 26.1% were receiving a low dose of ziprasidone, 25.7% a medium dose, and 48.3% a high dose. Among the propensity score-matched dosing groups, the respective mean time to discontinuation for low, medium, and high doses was 90.5, 117.2, and 201.6d within the schizophrenia/schizoaffective disorder cohort and 84.6, 110.7, and 173.2d within the bipolar cohort (p<0.0001 for all comparisons). The hazard ratios for discontinuing therapy were significantly lower for the medium- (0.84, 0.84) and high-dose (0.57, 0.60) groups relative to the low-dose group in schizophrenia/schizoaffective disorder and bipolar disorder, respectively.

Conclusions

Patients with schizophrenia/schizoaffective or bipolar disorders receiving ziprasidone 120–160mg/d experienced a statistically significant lower discontinuation rate compared with those receiving lower doses.

Keywords: Bipolar disorder, Dose, Effectiveness, Schizophrenia, Ziprasidone

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PII: S0920-9964(09)00442-3

doi:10.1016/j.schres.2009.09.023

Schizophrenia Research
Volume 115, Issue 2 , Pages 115-120, December 2009