Effectiveness of the Information Technology-Aided Program of Relapse Prevention in Schizophrenia (ITAREPS): A Randomized, Controlled, Double-Blind Study

被引:59
作者
Spaniel, Filip [1 ]
Hrdlicka, Jan [2 ]
Novak, Tomas [1 ]
Kozeny, Jiri [1 ]
Hoeschl, Cyril [1 ]
Mohr, Pavel [1 ]
Motlova, Lucie Bankovska [1 ]
机构
[1] Charles Univ Prague, Fac Med 3, Prague Psychiat Ctr, Ctr Neuropsychiat Studies, Prague 18103 8, Czech Republic
[2] Czech Tech Univ, Fac Elect Engn, Dept Cybernet, CR-16635 Prague, Czech Republic
关键词
schizophrenia; psychotic disorders; relapse prevention; hospitalizations; antipsychotic medication; information technology; FOLLOW-UP; THERAPY; PREDICTION; SYMPTOMS; EPISODE; COSTS; SIGNS;
D O I
10.1097/01.pra.0000416017.45591.c1
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Purpose. To evaluate the effectiveness of the Information Technology-Aided Program of Re lapse Prevention in Schizophrenia (ITAREPS). Methods. Relapse-prone outpatients with schizophrenia or schizoaffective disorder were randomized to the active (n = 75) or control group (n = 71). In the active arm, according to the protocol, investigators were prompted to increase the antipsychotic dose upon occurrence of a pharmacological intervention requiring event (PIRE) detected by ITAREPS. Results. Intention-to-treat (ITT) analysis found no between-group difference in the hospitalization-free survival rate at 12 months. However, the trial suffered from high non-adherence of investigators in the active group, with no antipsychotic dose increase in 61% of PIREs. Furthermore, Cox regression analysis showed a 11-fold increased risk of hospitalization in the absence of pharmacological intervention following a PIRE (hazard ratio [HR] = 10.8; 95% confidence interval [CI] 1.4-80.0; p = 0.002). Therefore, a post-hoc as-treated analysis was performed, which demonstrated a nine-fold reduction in the risk of hospitalization in ITAREPS Algorithm-Adherers (IAAs, n = 25) compared with the ITAREPS Non-interventional group (INIs, n = 70; Kaplan-Meier survival analysis, HR = 0.11, 95% CI 0.05-0.28, p = 0.009; number needed to treat [NNT] = 4, 95% CI 3-10). A significant difference in favor of the IAA group was seen in the number of inpatient days (p < 0.05) and costs (p < 0.05). Conclusion. Future ITAREPS trials should target the underlying mechanisms that cause low investigator adherence to the program. Trial registration: Clinical Trials NCT00712660 (Journal of Psychiatric Practice 2012; 18: 269-280)
引用
收藏
页码:269 / 280
页数:12
相关论文
共 30 条
[1]   Antipsychotic Dose Equivalents and Dose-Years: A Standardized Method for Comparing Exposure to Different Drugs [J].
Andreasen, Nancy C. ;
Pressler, Marcus ;
Nopoulos, Peg ;
Miller, Del ;
Ho, Beng-Choon .
BIOLOGICAL PSYCHIATRY, 2010, 67 (03) :255-262
[2]  
[Anonymous], DIAGN STAT MAN MENT
[3]   PREDICTING RELAPSE IN SCHIZOPHRENIA - THE DEVELOPMENT AND IMPLEMENTATION OF AN EARLY SIGNS MONITORING-SYSTEM USING PATIENTS AND FAMILIES AS OBSERVERS, A PRELIMINARY INVESTIGATION [J].
BIRCHWOOD, M ;
SMITH, J ;
MACMILLAN, F ;
HOGG, B ;
PRASAD, R ;
HARVEY, C ;
BERING, S .
PSYCHOLOGICAL MEDICINE, 1989, 19 (03) :649-656
[4]   Early intervention in psychotic relapse [J].
Birchwood, M ;
Spencer, E .
CLINICAL PSYCHOLOGY REVIEW, 2001, 21 (08) :1211-1226
[5]   Psychosis and brain volume changes during the first five years of schizophrenia [J].
Cahn, W. ;
Rais, M. ;
Stigter, F. P. ;
van Haren, N. E. M. ;
Caspers, E. ;
Pol, H. E. Hulshoff ;
Xu, Z. ;
Schnack, H. G. ;
Kahn, R. S. .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2009, 19 (02) :147-151
[6]   A comparison of risperidone and haloperidol for the prevention of relapse in patients with schizophrenia [J].
Csernansky, JG ;
Mahmoud, R ;
Brenner, R .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (01) :16-22
[7]   Revisiting the relapse predictive validity of prodromal symptoms in schizophrenia [J].
Gaebel, Wolfgang ;
Riesbeck, Mathias .
SCHIZOPHRENIA RESEARCH, 2007, 95 (1-3) :19-29
[8]   PREDICTION OF OUTCOME FOLLOWING A FIRST EPISODE OF SCHIZOPHRENIA - A FOLLOW-UP-STUDY OF NORTHWICK PARK FIRST EPISODE STUDY SUBJECTS [J].
GEDDES, J ;
MERCER, G ;
FRITH, CD ;
MACMILLAN, F ;
OWENS, DGC ;
JOHNSTONE, EC .
BRITISH JOURNAL OF PSYCHIATRY, 1994, 165 :664-668
[9]  
Glazer WM, 1996, J CLIN PSYCHIAT, V57, P337
[10]   Sex differences in outcome and recovery for schizophrenia and other psychotic and nonpsychotic disorders [J].
Grossman, Linda S. ;
Harrow, Martin ;
Rosen, Cherise ;
Faull, Robert .
PSYCHIATRIC SERVICES, 2006, 57 (06) :844-850