Medication burden reduction and early clinical benefit through aripiprazole once monthly in schizophrenia patients with polypharmacy
Antipsychotic polypharmacy is commonly used in clinical settings, with a growing trend in using long-acting injections to mitigate many side effects of polypharmacy. A previous study demonstrated that long-acting aripiprazole once-monthly (AOM) injection increased treatment adherence, restored funct...
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Published in: | Progress in neuro-psychopharmacology & biological psychiatry Vol. 135; p. 111115 |
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Abstract | Antipsychotic polypharmacy is commonly used in clinical settings, with a growing trend in using long-acting injections to mitigate many side effects of polypharmacy. A previous study demonstrated that long-acting aripiprazole once-monthly (AOM) injection increased treatment adherence, restored functionality, and improved symptoms. However, there is insufficient evidence to demonstrate the therapeutic effects of AOM in polypharmacy practice. This observational study aimed to investigate the real-world clinical benefits and effectiveness of AOM by assessing changes in drug dosage, the number of drugs, clinical functioning, psychotic symptoms, and the duration of drug efficacy.
Study participants were recruited from eight study sites, with the baseline visit marking the initiation of drug treatment. Clinical and demographic data were collected from medical records at screening, baseline, and months 1, 3, 6, 9, and 12. Over 12 months, we analyzed changes in drug dosage, the number of drugs, and scores of the Positive and Negative Syndrome Scale-6 (PANSS-6), Global Assessment of Functioning (GAF), and Clinical Global Impression-Severity (CGIS).
Data from 139 participants were analyzed. Total 12-month antipsychotic doses calculated in chlorpromazine equivalents (CPE) were reduced by 32.6%. A comparison of total monthly antipsychotic doses in CPE between the first and last months showed a 24.6% reduction in the dose. Additionally, the quantity of benzodiazepine tablets/capsules, total benzodiazepine doses calculated in lorazepam equivalents, and quantity of tablets/capsules of mood stabilizers, anticholinergics, and beta blockers were significantly reduced. GAF scores increased by 14.1% over 12 months, and PANSS-6 total scores reduced by 17.3% over 12 months, with significant differences observed from month 1 and baseline, respectively. The scores steadily improved until month 9 compared to those of the previous months, continuing to improve through month 12. The CGI-S score reduced by 14.3% over 12 months, showing a significant decrease from month 1 and a steady improvement until month 6, maintaining this improvement until month 12.
In conclusion, this study demonstrated the early effectiveness of AOM in treating Korean patients with schizophrenia on polypharmacy. AOM improved function and clinical symptoms in patients with schizophrenia from treatment onset and caused a decrease in the quantity and dosage of drugs taken by the patients.
•AOM decreases patients' total antipsychotic drug intake.•AOM efficacy is evident from treatment onset and symptoms improve until month 9.•AOM improves function and symptoms in schizophrenia that lasts till month 12. |
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AbstractList | Antipsychotic polypharmacy is commonly used in clinical settings, with a growing trend in using long-acting injections to mitigate many side effects of polypharmacy. A previous study demonstrated that long-acting aripiprazole once-monthly (AOM) injection increased treatment adherence, restored functionality, and improved symptoms. However, there is insufficient evidence to demonstrate the therapeutic effects of AOM in polypharmacy practice. This observational study aimed to investigate the real-world clinical benefits and effectiveness of AOM by assessing changes in drug dosage, the number of drugs, clinical functioning, psychotic symptoms, and the duration of drug efficacy. Study participants were recruited from eight study sites, with the baseline visit marking the initiation of drug treatment. Clinical and demographic data were collected from medical records at screening, baseline, and months 1, 3, 6, 9, and 12. Over 12 months, we analyzed changes in drug dosage, the number of drugs, and scores of the Positive and Negative Syndrome Scale-6 (PANSS-6), Global Assessment of Functioning (GAF), and Clinical Global Impression-Severity (CGIS). Data from 139 participants were analyzed. Total 12-month antipsychotic doses calculated in chlorpromazine equivalents (CPE) were reduced by 32.6%. A comparison of total monthly antipsychotic doses in CPE between the first and last months showed a 24.6% reduction in the dose. Additionally, the quantity of benzodiazepine tablets/capsules, total benzodiazepine doses calculated in lorazepam equivalents, and quantity of tablets/capsules of mood stabilizers, anticholinergics, and beta blockers were significantly reduced. GAF scores increased by 14.1% over 12 months, and PANSS-6 total scores reduced by 17.3% over 12 months, with significant differences observed from month 1 and baseline, respectively. The scores steadily improved until month 9 compared to those of the previous months, continuing to improve through month 12. The CGI-S score reduced by 14.3% over 12 months, showing a significant decrease from month 1 and a steady improvement until month 6, maintaining this improvement until month 12. In conclusion, this study demonstrated the early effectiveness of AOM in treating Korean patients with schizophrenia on polypharmacy. AOM improved function and clinical symptoms in patients with schizophrenia from treatment onset and caused a decrease in the quantity and dosage of drugs taken by the patients.Antipsychotic polypharmacy is commonly used in clinical settings, with a growing trend in using long-acting injections to mitigate many side effects of polypharmacy. A previous study demonstrated that long-acting aripiprazole once-monthly (AOM) injection increased treatment adherence, restored functionality, and improved symptoms. However, there is insufficient evidence to demonstrate the therapeutic effects of AOM in polypharmacy practice. This observational study aimed to investigate the real-world clinical benefits and effectiveness of AOM by assessing changes in drug dosage, the number of drugs, clinical functioning, psychotic symptoms, and the duration of drug efficacy. Study participants were recruited from eight study sites, with the baseline visit marking the initiation of drug treatment. Clinical and demographic data were collected from medical records at screening, baseline, and months 1, 3, 6, 9, and 12. Over 12 months, we analyzed changes in drug dosage, the number of drugs, and scores of the Positive and Negative Syndrome Scale-6 (PANSS-6), Global Assessment of Functioning (GAF), and Clinical Global Impression-Severity (CGIS). Data from 139 participants were analyzed. Total 12-month antipsychotic doses calculated in chlorpromazine equivalents (CPE) were reduced by 32.6%. A comparison of total monthly antipsychotic doses in CPE between the first and last months showed a 24.6% reduction in the dose. Additionally, the quantity of benzodiazepine tablets/capsules, total benzodiazepine doses calculated in lorazepam equivalents, and quantity of tablets/capsules of mood stabilizers, anticholinergics, and beta blockers were significantly reduced. GAF scores increased by 14.1% over 12 months, and PANSS-6 total scores reduced by 17.3% over 12 months, with significant differences observed from month 1 and baseline, respectively. The scores steadily improved until month 9 compared to those of the previous months, continuing to improve through month 12. The CGI-S score reduced by 14.3% over 12 months, showing a significant decrease from month 1 and a steady improvement until month 6, maintaining this improvement until month 12. In conclusion, this study demonstrated the early effectiveness of AOM in treating Korean patients with schizophrenia on polypharmacy. AOM improved function and clinical symptoms in patients with schizophrenia from treatment onset and caused a decrease in the quantity and dosage of drugs taken by the patients. Antipsychotic polypharmacy is commonly used in clinical settings, with a growing trend in using long-acting injections to mitigate many side effects of polypharmacy. A previous study demonstrated that long-acting aripiprazole once-monthly (AOM) injection increased treatment adherence, restored functionality, and improved symptoms. However, there is insufficient evidence to demonstrate the therapeutic effects of AOM in polypharmacy practice. This observational study aimed to investigate the real-world clinical benefits and effectiveness of AOM by assessing changes in drug dosage, the number of drugs, clinical functioning, psychotic symptoms, and the duration of drug efficacy. Study participants were recruited from eight study sites, with the baseline visit marking the initiation of drug treatment. Clinical and demographic data were collected from medical records at screening, baseline, and months 1, 3, 6, 9, and 12. Over 12 months, we analyzed changes in drug dosage, the number of drugs, and scores of the Positive and Negative Syndrome Scale-6 (PANSS-6), Global Assessment of Functioning (GAF), and Clinical Global Impression-Severity (CGIS). Data from 139 participants were analyzed. Total 12-month antipsychotic doses calculated in chlorpromazine equivalents (CPE) were reduced by 32.6%. A comparison of total monthly antipsychotic doses in CPE between the first and last months showed a 24.6% reduction in the dose. Additionally, the quantity of benzodiazepine tablets/capsules, total benzodiazepine doses calculated in lorazepam equivalents, and quantity of tablets/capsules of mood stabilizers, anticholinergics, and beta blockers were significantly reduced. GAF scores increased by 14.1% over 12 months, and PANSS-6 total scores reduced by 17.3% over 12 months, with significant differences observed from month 1 and baseline, respectively. The scores steadily improved until month 9 compared to those of the previous months, continuing to improve through month 12. The CGI-S score reduced by 14.3% over 12 months, showing a significant decrease from month 1 and a steady improvement until month 6, maintaining this improvement until month 12. In conclusion, this study demonstrated the early effectiveness of AOM in treating Korean patients with schizophrenia on polypharmacy. AOM improved function and clinical symptoms in patients with schizophrenia from treatment onset and caused a decrease in the quantity and dosage of drugs taken by the patients. Antipsychotic polypharmacy is commonly used in clinical settings, with a growing trend in using long-acting injections to mitigate many side effects of polypharmacy. A previous study demonstrated that long-acting aripiprazole once-monthly (AOM) injection increased treatment adherence, restored functionality, and improved symptoms. However, there is insufficient evidence to demonstrate the therapeutic effects of AOM in polypharmacy practice. This observational study aimed to investigate the real-world clinical benefits and effectiveness of AOM by assessing changes in drug dosage, the number of drugs, clinical functioning, psychotic symptoms, and the duration of drug efficacy. Study participants were recruited from eight study sites, with the baseline visit marking the initiation of drug treatment. Clinical and demographic data were collected from medical records at screening, baseline, and months 1, 3, 6, 9, and 12. Over 12 months, we analyzed changes in drug dosage, the number of drugs, and scores of the Positive and Negative Syndrome Scale-6 (PANSS-6), Global Assessment of Functioning (GAF), and Clinical Global Impression-Severity (CGIS). Data from 139 participants were analyzed. Total 12-month antipsychotic doses calculated in chlorpromazine equivalents (CPE) were reduced by 32.6%. A comparison of total monthly antipsychotic doses in CPE between the first and last months showed a 24.6% reduction in the dose. Additionally, the quantity of benzodiazepine tablets/capsules, total benzodiazepine doses calculated in lorazepam equivalents, and quantity of tablets/capsules of mood stabilizers, anticholinergics, and beta blockers were significantly reduced. GAF scores increased by 14.1% over 12 months, and PANSS-6 total scores reduced by 17.3% over 12 months, with significant differences observed from month 1 and baseline, respectively. The scores steadily improved until month 9 compared to those of the previous months, continuing to improve through month 12. The CGI-S score reduced by 14.3% over 12 months, showing a significant decrease from month 1 and a steady improvement until month 6, maintaining this improvement until month 12. In conclusion, this study demonstrated the early effectiveness of AOM in treating Korean patients with schizophrenia on polypharmacy. AOM improved function and clinical symptoms in patients with schizophrenia from treatment onset and caused a decrease in the quantity and dosage of drugs taken by the patients. •AOM decreases patients' total antipsychotic drug intake.•AOM efficacy is evident from treatment onset and symptoms improve until month 9.•AOM improves function and symptoms in schizophrenia that lasts till month 12. |
ArticleNumber | 111115 |
Author | Bang, Minji Chang, Jhin-Goo Kim, Min-Kyoung Yang, Hyeryun Lee, Sang Min Jung, Soo Bong Moon, Jiwan Shin, Dong-Won Cho, Sung Joon Moon, Suhyeon Jung, Sra Kim, Won-Hyoung Kim, Eun Soo Kim, Jangrae Lee, Mi Yeon |
Author_xml | – sequence: 1 givenname: Jiwan surname: Moon fullname: Moon, Jiwan organization: Department of Psychiatry, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul 03181, Republic of Korea – sequence: 2 givenname: Hyeryun surname: Yang fullname: Yang, Hyeryun organization: Department of Psychiatry, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul 03181, Republic of Korea – sequence: 3 givenname: Sra surname: Jung fullname: Jung, Sra organization: Department of Psychiatry, CHA Ilsan Medical Center, CHA University School of Medicine, Goyang 10414, Republic of Korea – sequence: 4 givenname: Soo Bong surname: Jung fullname: Jung, Soo Bong organization: Department of Psychiatry, Keyo Hospital, Uiwang 16062, Republic of Korea – sequence: 5 givenname: Jhin-Goo surname: Chang fullname: Chang, Jhin-Goo organization: Department of Psychiatry, Myongji Hospital, Hanyang University College of Medicine, Goyang 10475, Republic of Korea – sequence: 6 givenname: Won-Hyoung surname: Kim fullname: Kim, Won-Hyoung organization: Department of Psychiatry, Inha University Hospital, Incheon 22332, Republic of Korea – sequence: 7 givenname: Sang Min surname: Lee fullname: Lee, Sang Min organization: Department of Psychiatry, Kyung Hee University Hospital, Kyung Hee University School of Medicine, Seoul 02447, Republic of Korea – sequence: 8 givenname: Jangrae surname: Kim fullname: Kim, Jangrae organization: Department of Psychiatry, National Medical Center, Seoul 04564, Republic of Korea – sequence: 9 givenname: Minji surname: Bang fullname: Bang, Minji organization: Department of Psychiatry, CHA Bundang Medical Center, CHA University School of Medicine, Seongnam 13496, Republic of Korea – sequence: 10 givenname: Min-Kyoung surname: Kim fullname: Kim, Min-Kyoung organization: Department of Psychiatry, CHA Ilsan Medical Center, CHA University School of Medicine, Goyang 10414, Republic of Korea – sequence: 11 givenname: Dong-Won surname: Shin fullname: Shin, Dong-Won organization: Department of Psychiatry, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul 03181, Republic of Korea – sequence: 12 givenname: Mi Yeon surname: Lee fullname: Lee, Mi Yeon organization: Division of Biostatistics, Department of R&D Management, Samsung Kangbuk Hospital, Seoul 03181, Republic of Korea – sequence: 13 givenname: Suhyeon surname: Moon fullname: Moon, Suhyeon organization: Division of Biostatistics, Department of R&D Management, Samsung Kangbuk Hospital, Seoul 03181, Republic of Korea – sequence: 14 givenname: Eun Soo surname: Kim fullname: Kim, Eun Soo email: eunsoo421.kim@samsung.com organization: Department of Psychiatry, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul 03181, Republic of Korea – sequence: 15 givenname: Sung Joon surname: Cho fullname: Cho, Sung Joon email: sungjoon.cho@samsung.com organization: Department of Psychiatry, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul 03181, Republic of Korea |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39116930$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1177/02698811221131992 10.1097/01.jcp.0000218407.10362.6e 10.9758/cpn.2021.19.3.434 10.1176/appi.ajp.2020.177901 10.1111/pcn.12275 10.1002/cpdd.1022 10.1111/acps.12952 10.1016/j.schres.2013.06.041 10.18773/austprescr.2015.055 10.1007/s12325-018-0785-y 10.1176/appi.ajp.2009.09060802 10.1186/s12888-019-2103-x 10.1177/0269881121996890 10.1111/acps.12526 10.1192/j.eurpsy.2022.27 10.1186/s12888-020-02488-1 10.1111/bcpt.13384 10.1186/s12888-018-1946-x 10.1038/sj.npp.1301147 10.9758/cpn.2020.18.1.153 10.1016/S0149-2918(03)80222-9 10.9758/cpn.2021.19.2.233 10.3109/15622975.2012.696143 |
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Keywords | DSM-5 AE Schizophrenia Long-acting injectable Functional improvement GAF Antipsychotics SD Polypharmacy CPE PANSS GCI-S AOM |
Language | English |
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References | Nielsen, Kølbæk, Dines, Pedersen, Danielsen, Holmgård, Wissing, Esbøl, Fuglsang, Nguyen, Mors, Opler, Correll, Østergaard (bb0060) 2022; 36 Srivastava, Arora, Kataria, Cappelleri, Sadosky, Peterson (bb0120) 2013; 7 Leucht, Kane, Etschel, Kissling, Hamann, Engel (bb0045) 2006; 31 Pae, Han, Bahk, Lee, Patkar, Masand (bb0080) 2020; 18 Østergaard, Foldager, Mors, Bech, Correll (bb0075) 2018; 138 Gardner, Murphy, O’Donnell, Centorrino, Baldessarini (bb0020) 2010; 167 Schottle, Janetzky, Luedecke, Beck, Correll, Wiedemann (bb0105) 2018; 18 Richter, Anton, Koch, Dennett (bb0100) 2003; 25 Yan, Greene, Chang, Hartry, Touya, Broder (bb0130) 2018; 35 Wang, Raoufinia, Bihorel, Passarell, Mallikaarjun, Phillips (bb0125) 2022; 11 Pae, Han, Bahk, Lee, Patkar, Masand (bb0085) 2021; 19 Østergaard, Lemming, Mors, Correll, Bech (bb0065) 2016; 133 Brett, Murnion (bb0010) 2015; 38 Pae, Han, Bahk, Lee, Patkar, Masand (bb0090) 2021; 19 Inada, Inagaki (bb0030) 2015; 69 Baandrup (bb0005) 2020; 126 Schottle, Janetzky, Luedecke, Beck, Correll, Wiedemann (bb0110) 2020; 20 Keepers, Fochtmann, Anzia, Benjamin, Lyness, Mojtabai, Servis, Walaszek, Buckley, Lenzenweger, Young, Degenhardt, Hong (bb0035) 2020; 177 Kølbæk, Dines, Holm, Blicher, Sørensen, O’Leary, Feller, Buus, Nielsen, Opler, Mors, Correll, Østergaard (bb0040) 2021; 35 Rabinowitz, Mehnert, Eerdekens (bb0095) 2006; 26 Østergaard, Opler, Correll (bb0070) 2017; 14 Mustafa, Bougie, Miguelez, Clerzius, Rampakakis, Proulx, Malla (bb0055) 2019; 19 Mallikaarjun, Kane, Bricmont, McQuade, Carson, Sanchez, Forbes, Fleischhacker (bb0050) 2013; 150 Schöttle, Clerzius, Janetzky, Oluboka, Roy, Therrien, Wiedemann (bb0115) 2022; 65 Hasan, Falkai, Wobrock, Lieberman, Glenthoj, Gattaz, Thibaut, Möller (bb0025) 2012; 13 FJ, B, L, MA (bb0015) 2016 Rabinowitz (10.1016/j.pnpbp.2024.111115_bb0095) 2006; 26 Østergaard (10.1016/j.pnpbp.2024.111115_bb0070) 2017; 14 Østergaard (10.1016/j.pnpbp.2024.111115_bb0065) 2016; 133 Schottle (10.1016/j.pnpbp.2024.111115_bb0110) 2020; 20 FJ (10.1016/j.pnpbp.2024.111115_bb0015) Pae (10.1016/j.pnpbp.2024.111115_bb0080) 2020; 18 Pae (10.1016/j.pnpbp.2024.111115_bb0085) 2021; 19 Wang (10.1016/j.pnpbp.2024.111115_bb0125) 2022; 11 Kølbæk (10.1016/j.pnpbp.2024.111115_bb0040) 2021; 35 Nielsen (10.1016/j.pnpbp.2024.111115_bb0060) 2022; 36 Schottle (10.1016/j.pnpbp.2024.111115_bb0105) 2018; 18 Gardner (10.1016/j.pnpbp.2024.111115_bb0020) 2010; 167 Yan (10.1016/j.pnpbp.2024.111115_bb0130) 2018; 35 Leucht (10.1016/j.pnpbp.2024.111115_bb0045) 2006; 31 Pae (10.1016/j.pnpbp.2024.111115_bb0090) 2021; 19 Schöttle (10.1016/j.pnpbp.2024.111115_bb0115) 2022; 65 Baandrup (10.1016/j.pnpbp.2024.111115_bb0005) 2020; 126 Hasan (10.1016/j.pnpbp.2024.111115_bb0025) 2012; 13 Mustafa (10.1016/j.pnpbp.2024.111115_bb0055) 2019; 19 Østergaard (10.1016/j.pnpbp.2024.111115_bb0075) 2018; 138 Mallikaarjun (10.1016/j.pnpbp.2024.111115_bb0050) 2013; 150 Inada (10.1016/j.pnpbp.2024.111115_bb0030) 2015; 69 Srivastava (10.1016/j.pnpbp.2024.111115_bb0120) 2013; 7 Brett (10.1016/j.pnpbp.2024.111115_bb0010) 2015; 38 Richter (10.1016/j.pnpbp.2024.111115_bb0100) 2003; 25 Keepers (10.1016/j.pnpbp.2024.111115_bb0035) 2020; 177 |
References_xml | – volume: 167 start-page: 686 year: 2010 end-page: 693 ident: bb0020 article-title: International consensus study of antipsychotic dosing publication-title: Am. J. Psychiatry contributor: fullname: Baldessarini – volume: 69 start-page: 440 year: 2015 end-page: 447 ident: bb0030 article-title: Psychotropic dose equivalence in Japan publication-title: Psychiatry Clin. Neurosci. contributor: fullname: Inagaki – volume: 13 start-page: 318 year: 2012 end-page: 378 ident: bb0025 article-title: World Federation of Societies of biological psychiatry (WFSBP) guidelines for biological treatment of schizophrenia, part 1: update 2012 on the acute treatment of schizophrenia and the management of treatment resistance publication-title: World J. Biol. Psychiatry contributor: fullname: Möller – volume: 65 start-page: 1 year: 2022 end-page: 28 ident: bb0115 article-title: Real-world effectiveness of aripiprazole once-monthly REACT study: pooled analysis of two noninterventional studies publication-title: Eur. Psychiatry contributor: fullname: Wiedemann – volume: 150 start-page: 281 year: 2013 end-page: 288 ident: bb0050 article-title: Pharmacokinetics, tolerability and safety of aripiprazole once-monthly in adult schizophrenia: an open-label, parallel-arm, multiple-dose study publication-title: Schizophr. Res. contributor: fullname: Fleischhacker – volume: 138 start-page: 420 year: 2018 end-page: 431 ident: bb0075 article-title: The validity and sensitivity of PANSS-6 in treatment-resistant schizophrenia publication-title: Acta Psychiatr. Scand. contributor: fullname: Correll – volume: 177 start-page: 868 year: 2020 end-page: 872 ident: bb0035 article-title: The American Psychiatric Association practice guideline for the treatment of patients with schizophrenia publication-title: Am. J. Psychiatry contributor: fullname: Hong – volume: 35 start-page: 1612 year: 2018 end-page: 1625 ident: bb0130 article-title: Medication adherence and discontinuation of aripiprazole once-monthly 400 mg (AOM 400) versus Oral antipsychotics in patients with schizophrenia or bipolar I disorder: a real-world study using US claims data publication-title: Adv. Ther. contributor: fullname: Broder – volume: 133 start-page: 436 year: 2016 end-page: 444 ident: bb0065 article-title: PANSS-6: a brief rating scale for the measurement of severity in schizophrenia publication-title: Acta Psychiatr. Scand. contributor: fullname: Bech – volume: 35 start-page: 1081 year: 2021 end-page: 1090 ident: bb0040 article-title: Clinical validation of ratings on the six-item positive and negative syndrome scale obtained via the simplified negative and positive symptoms interview publication-title: J. Psychopharmacol. contributor: fullname: Østergaard – volume: 18 start-page: 365 year: 2018 ident: bb0105 article-title: Effectiveness of aripiprazole once-monthly in schizophrenia patients pretreated with oral aripiprazole: a 6-month, real-life non-interventional study publication-title: BMC Psychiatry contributor: fullname: Wiedemann – volume: 36 start-page: 1208 year: 2022 end-page: 1217 ident: bb0060 article-title: Validation of ratings on the six-item positive and negative syndrome scale obtained via the simplified negative and positive symptoms interview among outpatients with schizophrenia publication-title: J. Psychopharmacol. contributor: fullname: Østergaard – year: 2016 ident: bb0015 article-title: Investigating the Role of Benzodiazepines in Drug-Related Mortality: A Systematic Review Undertaken on Behalf of the Scottish National Forum on Drug-Related Deaths. N. H. Scotland contributor: fullname: MA – volume: 19 start-page: 114 year: 2019 ident: bb0055 article-title: Real-life assessment of aripiprazole monthly (Abilify Maintena) in schizophrenia: a Canadian naturalistic non-interventional prospective cohort study publication-title: BMC Psychiatry contributor: fullname: Malla – volume: 7 start-page: 419 year: 2013 end-page: 434 ident: bb0120 article-title: Impact of reducing dosing frequency on adherence to oral therapies: a literature review and meta-analysis publication-title: Patient Prefer. Adherence contributor: fullname: Peterson – volume: 18 start-page: 153 year: 2020 end-page: 158 ident: bb0080 article-title: Effectiveness and tolerability of switching to aripiprazole once monthly from antipsychotic polypharmacy and/or other long acting injectable antipsychotics for patients with schizophrenia in routine practice: a retrospective, observation study publication-title: Clin. Psychopharmacol. Neurosci. contributor: fullname: Masand – volume: 14 start-page: 68 year: 2017 end-page: 72 ident: bb0070 article-title: Bridging the measurement gap between research and clinical Care in Schizophrenia: positive and negative syndrome Scale-6 (PANSS-6) and other assessments based on the simplified negative and positive symptoms interview (SNAPSI) publication-title: Innov. Clin. Neurosci. contributor: fullname: Correll – volume: 19 start-page: 233 year: 2021 end-page: 242 ident: bb0085 article-title: Clinical benefit and utility of switching to aripiprazole once monthly in patients with antipsychotic polypharmacy or long acting injectable antipsychotics for patients with schizophrenia in routine practice: a retrospective, observation study publication-title: Clin. Psychopharmacol. Neurosci. contributor: fullname: Masand – volume: 19 start-page: 434 year: 2021 end-page: 448 ident: bb0090 article-title: Consideration of long-acting injectable antipsychotics for polypharmacy regimen in the treatment of schizophrenia: put it on the table or not? publication-title: Clin. Psychopharmacol. Neurosci. contributor: fullname: Masand – volume: 25 year: 2003 ident: bb0100 article-title: The impact of reducing dose frequency on health outcomes publication-title: Clin. Ther. contributor: fullname: Dennett – volume: 126 start-page: 183 year: 2020 end-page: 192 ident: bb0005 article-title: Polypharmacy in schizophrenia publication-title: Basic Clin. Pharmacol. Toxicol. contributor: fullname: Baandrup – volume: 38 start-page: 152 year: 2015 end-page: 155 ident: bb0010 article-title: Management of benzodiazepine misuse and dependence publication-title: Aust. Prescr. contributor: fullname: Murnion – volume: 31 start-page: 2318 year: 2006 end-page: 2325 ident: bb0045 article-title: Linking the PANSS, BPRS, and CGI: clinical implications publication-title: Neuropsychopharmacology contributor: fullname: Engel – volume: 11 start-page: 150 year: 2022 end-page: 164 ident: bb0125 article-title: Population pharmacokinetic modeling and exposure-response analysis for aripiprazole once monthly in subjects with schizophrenia publication-title: Clin. Pharmacol. Drug Develop. contributor: fullname: Phillips – volume: 26 start-page: 303 year: 2006 end-page: 307 ident: bb0095 article-title: To what extent do the PANSS and CGI-S overlap? publication-title: J. Clin. Psychopharmacol. contributor: fullname: Eerdekens – volume: 20 start-page: 77 year: 2020 ident: bb0110 article-title: The use of long-acting aripiprazole in a multi-center, prospective, uncontrolled, open-label, cohort study in Germany: a report on global assessment of functioning and the WHO wellbeing index publication-title: BMC Psychiatry contributor: fullname: Wiedemann – volume: 36 start-page: 1208 issue: 11 year: 2022 ident: 10.1016/j.pnpbp.2024.111115_bb0060 article-title: Validation of ratings on the six-item positive and negative syndrome scale obtained via the simplified negative and positive symptoms interview among outpatients with schizophrenia publication-title: J. Psychopharmacol. doi: 10.1177/02698811221131992 contributor: fullname: Nielsen – volume: 26 start-page: 303 issue: 3 year: 2006 ident: 10.1016/j.pnpbp.2024.111115_bb0095 article-title: To what extent do the PANSS and CGI-S overlap? publication-title: J. Clin. Psychopharmacol. doi: 10.1097/01.jcp.0000218407.10362.6e contributor: fullname: Rabinowitz – volume: 19 start-page: 434 issue: 3 year: 2021 ident: 10.1016/j.pnpbp.2024.111115_bb0090 article-title: Consideration of long-acting injectable antipsychotics for polypharmacy regimen in the treatment of schizophrenia: put it on the table or not? publication-title: Clin. Psychopharmacol. Neurosci. doi: 10.9758/cpn.2021.19.3.434 contributor: fullname: Pae – volume: 177 start-page: 868 issue: 9 year: 2020 ident: 10.1016/j.pnpbp.2024.111115_bb0035 article-title: The American Psychiatric Association practice guideline for the treatment of patients with schizophrenia publication-title: Am. J. Psychiatry doi: 10.1176/appi.ajp.2020.177901 contributor: fullname: Keepers – ident: 10.1016/j.pnpbp.2024.111115_bb0015 contributor: fullname: FJ – volume: 69 start-page: 440 issue: 8 year: 2015 ident: 10.1016/j.pnpbp.2024.111115_bb0030 article-title: Psychotropic dose equivalence in Japan publication-title: Psychiatry Clin. Neurosci. doi: 10.1111/pcn.12275 contributor: fullname: Inada – volume: 11 start-page: 150 issue: 2 year: 2022 ident: 10.1016/j.pnpbp.2024.111115_bb0125 article-title: Population pharmacokinetic modeling and exposure-response analysis for aripiprazole once monthly in subjects with schizophrenia publication-title: Clin. Pharmacol. Drug Develop. doi: 10.1002/cpdd.1022 contributor: fullname: Wang – volume: 7 start-page: 419 year: 2013 ident: 10.1016/j.pnpbp.2024.111115_bb0120 article-title: Impact of reducing dosing frequency on adherence to oral therapies: a literature review and meta-analysis publication-title: Patient Prefer. Adherence contributor: fullname: Srivastava – volume: 138 start-page: 420 issue: 5 year: 2018 ident: 10.1016/j.pnpbp.2024.111115_bb0075 article-title: The validity and sensitivity of PANSS-6 in treatment-resistant schizophrenia publication-title: Acta Psychiatr. Scand. doi: 10.1111/acps.12952 contributor: fullname: Østergaard – volume: 14 start-page: 68 issue: 11−12 year: 2017 ident: 10.1016/j.pnpbp.2024.111115_bb0070 article-title: Bridging the measurement gap between research and clinical Care in Schizophrenia: positive and negative syndrome Scale-6 (PANSS-6) and other assessments based on the simplified negative and positive symptoms interview (SNAPSI) publication-title: Innov. Clin. Neurosci. contributor: fullname: Østergaard – volume: 150 start-page: 281 issue: 1 year: 2013 ident: 10.1016/j.pnpbp.2024.111115_bb0050 article-title: Pharmacokinetics, tolerability and safety of aripiprazole once-monthly in adult schizophrenia: an open-label, parallel-arm, multiple-dose study publication-title: Schizophr. Res. doi: 10.1016/j.schres.2013.06.041 contributor: fullname: Mallikaarjun – volume: 38 start-page: 152 issue: 5 year: 2015 ident: 10.1016/j.pnpbp.2024.111115_bb0010 article-title: Management of benzodiazepine misuse and dependence publication-title: Aust. Prescr. doi: 10.18773/austprescr.2015.055 contributor: fullname: Brett – volume: 35 start-page: 1612 issue: 10 year: 2018 ident: 10.1016/j.pnpbp.2024.111115_bb0130 article-title: Medication adherence and discontinuation of aripiprazole once-monthly 400 mg (AOM 400) versus Oral antipsychotics in patients with schizophrenia or bipolar I disorder: a real-world study using US claims data publication-title: Adv. Ther. doi: 10.1007/s12325-018-0785-y contributor: fullname: Yan – volume: 167 start-page: 686 issue: 6 year: 2010 ident: 10.1016/j.pnpbp.2024.111115_bb0020 article-title: International consensus study of antipsychotic dosing publication-title: Am. J. Psychiatry doi: 10.1176/appi.ajp.2009.09060802 contributor: fullname: Gardner – volume: 19 start-page: 114 issue: 1 year: 2019 ident: 10.1016/j.pnpbp.2024.111115_bb0055 article-title: Real-life assessment of aripiprazole monthly (Abilify Maintena) in schizophrenia: a Canadian naturalistic non-interventional prospective cohort study publication-title: BMC Psychiatry doi: 10.1186/s12888-019-2103-x contributor: fullname: Mustafa – volume: 35 start-page: 1081 issue: 9 year: 2021 ident: 10.1016/j.pnpbp.2024.111115_bb0040 article-title: Clinical validation of ratings on the six-item positive and negative syndrome scale obtained via the simplified negative and positive symptoms interview publication-title: J. Psychopharmacol. doi: 10.1177/0269881121996890 contributor: fullname: Kølbæk – volume: 133 start-page: 436 issue: 6 year: 2016 ident: 10.1016/j.pnpbp.2024.111115_bb0065 article-title: PANSS-6: a brief rating scale for the measurement of severity in schizophrenia publication-title: Acta Psychiatr. Scand. doi: 10.1111/acps.12526 contributor: fullname: Østergaard – volume: 65 start-page: 1 issue: 1 year: 2022 ident: 10.1016/j.pnpbp.2024.111115_bb0115 article-title: Real-world effectiveness of aripiprazole once-monthly REACT study: pooled analysis of two noninterventional studies publication-title: Eur. Psychiatry doi: 10.1192/j.eurpsy.2022.27 contributor: fullname: Schöttle – volume: 20 start-page: 77 issue: 1 year: 2020 ident: 10.1016/j.pnpbp.2024.111115_bb0110 article-title: The use of long-acting aripiprazole in a multi-center, prospective, uncontrolled, open-label, cohort study in Germany: a report on global assessment of functioning and the WHO wellbeing index publication-title: BMC Psychiatry doi: 10.1186/s12888-020-02488-1 contributor: fullname: Schottle – volume: 126 start-page: 183 issue: 3 year: 2020 ident: 10.1016/j.pnpbp.2024.111115_bb0005 article-title: Polypharmacy in schizophrenia publication-title: Basic Clin. Pharmacol. Toxicol. doi: 10.1111/bcpt.13384 contributor: fullname: Baandrup – volume: 18 start-page: 365 issue: 1 year: 2018 ident: 10.1016/j.pnpbp.2024.111115_bb0105 article-title: Effectiveness of aripiprazole once-monthly in schizophrenia patients pretreated with oral aripiprazole: a 6-month, real-life non-interventional study publication-title: BMC Psychiatry doi: 10.1186/s12888-018-1946-x contributor: fullname: Schottle – volume: 31 start-page: 2318 issue: 10 year: 2006 ident: 10.1016/j.pnpbp.2024.111115_bb0045 article-title: Linking the PANSS, BPRS, and CGI: clinical implications publication-title: Neuropsychopharmacology doi: 10.1038/sj.npp.1301147 contributor: fullname: Leucht – volume: 18 start-page: 153 issue: 1 year: 2020 ident: 10.1016/j.pnpbp.2024.111115_bb0080 article-title: Effectiveness and tolerability of switching to aripiprazole once monthly from antipsychotic polypharmacy and/or other long acting injectable antipsychotics for patients with schizophrenia in routine practice: a retrospective, observation study publication-title: Clin. Psychopharmacol. Neurosci. doi: 10.9758/cpn.2020.18.1.153 contributor: fullname: Pae – volume: 25 issue: 8 year: 2003 ident: 10.1016/j.pnpbp.2024.111115_bb0100 article-title: The impact of reducing dose frequency on health outcomes publication-title: Clin. Ther. doi: 10.1016/S0149-2918(03)80222-9 contributor: fullname: Richter – volume: 19 start-page: 233 issue: 2 year: 2021 ident: 10.1016/j.pnpbp.2024.111115_bb0085 article-title: Clinical benefit and utility of switching to aripiprazole once monthly in patients with antipsychotic polypharmacy or long acting injectable antipsychotics for patients with schizophrenia in routine practice: a retrospective, observation study publication-title: Clin. Psychopharmacol. Neurosci. doi: 10.9758/cpn.2021.19.2.233 contributor: fullname: Pae – volume: 13 start-page: 318 issue: 5 year: 2012 ident: 10.1016/j.pnpbp.2024.111115_bb0025 article-title: World Federation of Societies of biological psychiatry (WFSBP) guidelines for biological treatment of schizophrenia, part 1: update 2012 on the acute treatment of schizophrenia and the management of treatment resistance publication-title: World J. Biol. Psychiatry doi: 10.3109/15622975.2012.696143 contributor: fullname: Hasan |
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Title | Medication burden reduction and early clinical benefit through aripiprazole once monthly in schizophrenia patients with polypharmacy |
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