Pregled bibliografske jedinice broj: 1011999
Efficacy and tolerability of the three-month formulation of paliperidone palmitate in first- episode schizophrenia patients
Efficacy and tolerability of the three-month formulation of paliperidone palmitate in first- episode schizophrenia patients // 17 th APA Anual Meeting
New York City (NY), Sjedinjene Američke Države, 2018. str. - (predavanje, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1011999 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Efficacy and tolerability of the three-month
formulation of paliperidone palmitate in first-
episode schizophrenia patients
Autori
Petrić, Daniela ; Rački, Valentino ; Gačo, Nadija ; Graovac, Mirjana ; Kaštelan, Ana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
17 th APA Anual Meeting
/ - , 2018
Skup
17th APA Anual Meeting
Mjesto i datum
New York City (NY), Sjedinjene Američke Države, 05.05.2018. - 09.05.2018
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
efficacy ; tolerability ; paliperidone palmitate ; first-episode ; schizophrenia patients
Sažetak
Introduction: Treating patients with first- episode schizophrenia is a challenge. Such patients have much to gain from controlled pharmacotherapy and even more to lose with a possible relapse. Treating patients with long- acting injectable antipsychotics avoids the issue of non-compliance, the biggest risk factor for relapse, while also improving the quality of life. Receiving a drug only four times a year can provide greater flexibility and convenience to our patients. Aim of the paper is to assess the therapeutic efficacy and tolerability of the three-month formulation of paliperidone palmitate long-acting injectable antipsychotic in first-episode schizophrenia patients. Methods: The research included 12 patients aged 19 to 24 years who were diagnosed in accordance with the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition. Patients were assessed four times over one year (after each drug application) using the following clinical scales: Positive and Negative Syndrome Scale, Clinical Global Impression – Severity and Improvement Scale, Personal and Social Performance Scale. Primary safety measures included incidence of adverse events. Results: All treated patients achieved remission. There was a statistically significant improvement in measured scales in all patients. There were no side-effects reported during the study period, with no relapse or new hospitalizations. Conclusion: The three-month formulation of paliperidone palmitate has proven to be effective and safe in our study, and has great potential to improve patient quality of life as well. Keywords: three-month paliperidone palmitate ; efficacy ; tolerability ; long-acting antipsychotics ; first-episode schizophrenia
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Rijeka,
Klinički bolnički centar Rijeka,
Fakultet zdravstvenih studija u Rijeci
Profili:
Valentino Rački
(autor)
Daniela Petrić
(autor)
Mirjana Graovac
(autor)
Ana Kaštelan
(autor)