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Blood lactate levels in patients receiving first- or second- generation antipsychotics
AIM: To compare the blood lactate levels between patients with psychotic disorder receiving first- and those receiving second-generation antipsychotics. METHODS: The study was conducted at the psychiatric inpatient and outpatient clinics of the Split Clinical Hospital from June 6, 2008 to October 10...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Croatian Medical Schools
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3046499/ https://www.ncbi.nlm.nih.gov/pubmed/21328719 http://dx.doi.org/10.3325/cmj.2011.52.41 |
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author | Glavina, Trpimir Mrass, Damir Dodig, Tajana Glavina, Gordana Pranić, Shelly Uglešić, Boran |
author_facet | Glavina, Trpimir Mrass, Damir Dodig, Tajana Glavina, Gordana Pranić, Shelly Uglešić, Boran |
author_sort | Glavina, Trpimir |
collection | PubMed |
description | AIM: To compare the blood lactate levels between patients with psychotic disorder receiving first- and those receiving second-generation antipsychotics. METHODS: The study was conducted at the psychiatric inpatient and outpatient clinics of the Split Clinical Hospital from June 6, 2008 to October 10, 2009. Sixty patients with psychotic disorder who were assigned to 6-month treatment were divided in two groups: 30 received haloperidol (first generation antipsychotic) and 30 received olanzapine (second generation antipsychotic). Blood lactate levels, other metabolic parameters, and scores on the extrapyramidal symptom rating scale were assessed. RESULTS: Patients receiving haloperidol had significantly higher blood lactate levels than patients receiving olanzapine (P < 0.001). They also more frequently had parkinsonism, which was significantly correlated with both haloperidol treatment at 1 month (P < 0.001) and 6 months (P = 0.016) and olanzapine treatment at baseline (P = 0.016), 3 months (P = 0.019), and 6 months (P = 0.021). Also, patients receiving haloperidol had significant correlation between blood lactate and dystonia at 1 month (P < 0.001) and 6 months (P = 0.012) and tardive dyskinesia at 1 month (P = 0.032). There was a significant difference between the treatment groups in lactate levels at all points from baseline to month 6 (P < 0.001). CONCLUSION: It is important to be aware of the potential effect of haloperidol treatment on increase in blood lactate levels and occurrence of extrapyramidal side effects. Therefore, alternative antipsychotics should be prescribed with lower risk of adverse side effects. TRIAL IDENTIFICATION NUMBER: NCT01139463 |
format | Text |
id | pubmed-3046499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Croatian Medical Schools |
record_format | MEDLINE/PubMed |
spelling | pubmed-30464992011-03-01 Blood lactate levels in patients receiving first- or second- generation antipsychotics Glavina, Trpimir Mrass, Damir Dodig, Tajana Glavina, Gordana Pranić, Shelly Uglešić, Boran Croat Med J Clinical Science AIM: To compare the blood lactate levels between patients with psychotic disorder receiving first- and those receiving second-generation antipsychotics. METHODS: The study was conducted at the psychiatric inpatient and outpatient clinics of the Split Clinical Hospital from June 6, 2008 to October 10, 2009. Sixty patients with psychotic disorder who were assigned to 6-month treatment were divided in two groups: 30 received haloperidol (first generation antipsychotic) and 30 received olanzapine (second generation antipsychotic). Blood lactate levels, other metabolic parameters, and scores on the extrapyramidal symptom rating scale were assessed. RESULTS: Patients receiving haloperidol had significantly higher blood lactate levels than patients receiving olanzapine (P < 0.001). They also more frequently had parkinsonism, which was significantly correlated with both haloperidol treatment at 1 month (P < 0.001) and 6 months (P = 0.016) and olanzapine treatment at baseline (P = 0.016), 3 months (P = 0.019), and 6 months (P = 0.021). Also, patients receiving haloperidol had significant correlation between blood lactate and dystonia at 1 month (P < 0.001) and 6 months (P = 0.012) and tardive dyskinesia at 1 month (P = 0.032). There was a significant difference between the treatment groups in lactate levels at all points from baseline to month 6 (P < 0.001). CONCLUSION: It is important to be aware of the potential effect of haloperidol treatment on increase in blood lactate levels and occurrence of extrapyramidal side effects. Therefore, alternative antipsychotics should be prescribed with lower risk of adverse side effects. TRIAL IDENTIFICATION NUMBER: NCT01139463 Croatian Medical Schools 2011-02 /pmc/articles/PMC3046499/ /pubmed/21328719 http://dx.doi.org/10.3325/cmj.2011.52.41 Text en Copyright © 2011 by the Croatian Medical Journal. All rights reserved. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Science Glavina, Trpimir Mrass, Damir Dodig, Tajana Glavina, Gordana Pranić, Shelly Uglešić, Boran Blood lactate levels in patients receiving first- or second- generation antipsychotics |
title | Blood lactate levels in patients receiving first- or second- generation antipsychotics |
title_full | Blood lactate levels in patients receiving first- or second- generation antipsychotics |
title_fullStr | Blood lactate levels in patients receiving first- or second- generation antipsychotics |
title_full_unstemmed | Blood lactate levels in patients receiving first- or second- generation antipsychotics |
title_short | Blood lactate levels in patients receiving first- or second- generation antipsychotics |
title_sort | blood lactate levels in patients receiving first- or second- generation antipsychotics |
topic | Clinical Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3046499/ https://www.ncbi.nlm.nih.gov/pubmed/21328719 http://dx.doi.org/10.3325/cmj.2011.52.41 |
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