A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Selection bias in clinical studies of first-episode psychosis: A follow-up study
Tekijät: Walta Maija, Laurikainen Heikki, Armio Reetta-Liina, From Tiina, Tolvanen Arvi, Salokangas Raimo KR, Hietala Jarmo
Kustantaja: ELSEVIER
Julkaisuvuosi: 2022
Journal: Schizophrenia Research
Tietokannassa oleva lehden nimi: SCHIZOPHRENIA RESEARCH
Lehden akronyymi: SCHIZOPHR RES
Vuosikerta: 246
Aloitussivu: 235
Lopetussivu: 240
Sivujen määrä: 6
ISSN: 0920-9964
DOI: https://doi.org/10.1016/j.schres.2022.06.022
Verkko-osoite: https://doi.org/10.1016/j.schres.2022.06.022
Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/detail/Publication/176044810
Objectives: Selection bias is a concern in studies on psychotic disorders due to high dropout rates and many eligibility criteria for inclusion. We studied how representative the first-episode psychosis study sample in the Turku Early Psychosis Study (TEPS) was.
Methods: We screened 3772 consecutive admissions to the clinical psychiatric services of Turku Psychiatry, Finland, between October 2011 and June 2016. A total of 193 subjects had first-episode psychosis and were suitable for TEPS. Out of 193 subjects, 101 participated (PA) and 92 did not participate (NPA) in TEPS due to refusal or contact problems. We retrospectively used patient register data to study whether NPA and PA groups differed in terms of clinical outcomes during 1-year follow-up.
Results: In overall sample, the NPA group had a significantly higher rate of discontinuation of clinical treatment than the PA group (48.9 % vs 29.7 %, p = 0.01). In the hospital-treated subsample chi-square tests did not indicate statistically significant differences between the NPA and PA groups in the rate of involuntary care (69.7 % vs 62.7 %, p = 0.34), coercive measures (36.0 % vs 22.7 %, p = 0.06), and readmissions during the follow-up (41.5 % vs 33.8 %, p = 0.31), respectively.
Conclusion: The differences in clinical outcomes and treatment characteristics in the non-participating and participating groups were relatively modest. The results do not support a major sample selection bias that would complicate the interpretation of results in this first-episode psychosis study.
Ladattava julkaisu This is an electronic reprint of the original article. |