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Prevalence of and Risk Factors for Dysglycemia in Patients Receiving Gatifloxacin and Levofloxacin in an Outpatient Setting

Study Objectives. To assess the prevalence of dysglycemia (hypoglycemia or hyperglycemia) associated with oral levofloxacin and gatifloxacin therapy in an outpatient setting, and to determine the characteristics of patients who developed dysglycemia while receiving either fluoroquinolone. Design. Re...

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Published in:Pharmacotherapy 2008-01, Vol.28 (1), p.82-89
Main Authors: LaPlante, Kerry L., Mersfelder, Tracey L., Ward, Kristina E., Quilliam, Brian J.
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description Study Objectives. To assess the prevalence of dysglycemia (hypoglycemia or hyperglycemia) associated with oral levofloxacin and gatifloxacin therapy in an outpatient setting, and to determine the characteristics of patients who developed dysglycemia while receiving either fluoroquinolone. Design. Retrospective medical record review. Setting. Outpatient clinic of a Veterans Affairs teaching hospital. Patients. A total of 1573 patients who received oral levofloxacin (343 patients), gatifloxacin (589 patients), or azithromycin (as a control, 641 patients) between June 1, 2004, and May 31, 2006. Measurements and Main Results. Dysglycemia occurred in 33 patients: 13 (2.2%), 9 (2.6%), and 11 (1.7%), respectively, of those in the gatifloxacin, levofloxacin, and azithromycin groups. Of 13 patients who experienced a hyperglycemic event, 11 (84.6%) had diabetes mellitus. After adjustment for confounding factors, neither levofloxacin nor gatifloxacin were associated with increased odds of developing a dysglycemic event compared with azithromycin. Multivariate analysis demonstrated that lack of downward dosage adjustment based on creatinine clearance (odds ratio [OR] 10.3, 95% confidence interval [CI] 3.8–27.6), presence of diabetes (OR 17.1, 95% CI 3.1–94.9), or treatment with insulin (OR 5.3, 95% CI 1.8–15.7) or sulfonylureas (OR 3.6, 95% CI 1.3–10.4) independently increased dysglycemia risk. Obesity (body mass index > 30 kg/m2) was independently protective (OR 0.22, 95% CI 0.09‐0.55) against dysglycemic events. Conclusion. Levofloxacin and gatifloxacin were not significantly associated with increased dysglycemic events compared with azithromycin. Lack of downward fluoroquinolone dosage adjustment for renal function, presence of diabetes, and treatment with insulin or sulfonylureas each independently increased the risk of dysglycemia. Obesity was independently protective against dysglycemia. More data are needed on the contributing effects of diabetes, fluoroquinolone dosage, and concomitant drug therapy so that an appropriate risk‐management strategy can be developed.
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To assess the prevalence of dysglycemia (hypoglycemia or hyperglycemia) associated with oral levofloxacin and gatifloxacin therapy in an outpatient setting, and to determine the characteristics of patients who developed dysglycemia while receiving either fluoroquinolone. Design. Retrospective medical record review. Setting. Outpatient clinic of a Veterans Affairs teaching hospital. Patients. A total of 1573 patients who received oral levofloxacin (343 patients), gatifloxacin (589 patients), or azithromycin (as a control, 641 patients) between June 1, 2004, and May 31, 2006. Measurements and Main Results. Dysglycemia occurred in 33 patients: 13 (2.2%), 9 (2.6%), and 11 (1.7%), respectively, of those in the gatifloxacin, levofloxacin, and azithromycin groups. Of 13 patients who experienced a hyperglycemic event, 11 (84.6%) had diabetes mellitus. After adjustment for confounding factors, neither levofloxacin nor gatifloxacin were associated with increased odds of developing a dysglycemic event compared with azithromycin. Multivariate analysis demonstrated that lack of downward dosage adjustment based on creatinine clearance (odds ratio [OR] 10.3, 95% confidence interval [CI] 3.8–27.6), presence of diabetes (OR 17.1, 95% CI 3.1–94.9), or treatment with insulin (OR 5.3, 95% CI 1.8–15.7) or sulfonylureas (OR 3.6, 95% CI 1.3–10.4) independently increased dysglycemia risk. Obesity (body mass index &gt; 30 kg/m2) was independently protective (OR 0.22, 95% CI 0.09‐0.55) against dysglycemic events. Conclusion. Levofloxacin and gatifloxacin were not significantly associated with increased dysglycemic events compared with azithromycin. Lack of downward fluoroquinolone dosage adjustment for renal function, presence of diabetes, and treatment with insulin or sulfonylureas each independently increased the risk of dysglycemia. Obesity was independently protective against dysglycemia. More data are needed on the contributing effects of diabetes, fluoroquinolone dosage, and concomitant drug therapy so that an appropriate risk‐management strategy can be developed.</description><identifier>ISSN: 0277-0008</identifier><identifier>EISSN: 1875-9114</identifier><identifier>DOI: 10.1592/phco.28.1.82</identifier><identifier>PMID: 18154478</identifier><identifier>CODEN: PHPYDQ</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject><![CDATA[Administration, Oral ; Adult ; Aged ; Aged, 80 and over ; Aminoacid disorders ; Anti-Bacterial Agents - administration & dosage ; Anti-Bacterial Agents - adverse effects ; Anti-Bacterial Agents - therapeutic use ; azithromycin ; Azithromycin - administration & dosage ; Azithromycin - adverse effects ; Azithromycin - therapeutic use ; Biological and medical sciences ; Creatinine - blood ; Diabetes Complications - drug therapy ; dysglycemias ; Errors of metabolism ; Female ; Fluoroquinolones - administration & dosage ; Fluoroquinolones - adverse effects ; Fluoroquinolones - chemistry ; Fluoroquinolones - therapeutic use ; gatifloxacin ; Hospitals, Veterans - statistics & numerical data ; Humans ; hyperglycemia ; Hyperglycemia - chemically induced ; Hyperglycemia - epidemiology ; hypoglycemia ; Hypoglycemia - chemically induced ; Hypoglycemia - epidemiology ; Levofloxacin ; Male ; Medical Records - statistics & numerical data ; Medical sciences ; Metabolic diseases ; Middle Aged ; Multivariate Analysis ; Ofloxacin - administration & dosage ; Ofloxacin - adverse effects ; Ofloxacin - therapeutic use ; outpatient ; Pharmacology. Drug treatments ; Prevalence ; Retrospective Studies ; Rhode Island - epidemiology ; Risk Factors]]></subject><ispartof>Pharmacotherapy, 2008-01, Vol.28 (1), p.82-89</ispartof><rights>2008 Pharmacotherapy Publications Inc.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3614-fadedb6dfc2497d083d98a7c8d9ecc2b92932282891274c0df301d83beae28533</citedby><cites>FETCH-LOGICAL-c3614-fadedb6dfc2497d083d98a7c8d9ecc2b92932282891274c0df301d83beae28533</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=19980025$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18154478$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LaPlante, Kerry L.</creatorcontrib><creatorcontrib>Mersfelder, Tracey L.</creatorcontrib><creatorcontrib>Ward, Kristina E.</creatorcontrib><creatorcontrib>Quilliam, Brian J.</creatorcontrib><title>Prevalence of and Risk Factors for Dysglycemia in Patients Receiving Gatifloxacin and Levofloxacin in an Outpatient Setting</title><title>Pharmacotherapy</title><addtitle>Pharmacotherapy</addtitle><description>Study Objectives. To assess the prevalence of dysglycemia (hypoglycemia or hyperglycemia) associated with oral levofloxacin and gatifloxacin therapy in an outpatient setting, and to determine the characteristics of patients who developed dysglycemia while receiving either fluoroquinolone. Design. Retrospective medical record review. Setting. Outpatient clinic of a Veterans Affairs teaching hospital. Patients. A total of 1573 patients who received oral levofloxacin (343 patients), gatifloxacin (589 patients), or azithromycin (as a control, 641 patients) between June 1, 2004, and May 31, 2006. Measurements and Main Results. Dysglycemia occurred in 33 patients: 13 (2.2%), 9 (2.6%), and 11 (1.7%), respectively, of those in the gatifloxacin, levofloxacin, and azithromycin groups. Of 13 patients who experienced a hyperglycemic event, 11 (84.6%) had diabetes mellitus. After adjustment for confounding factors, neither levofloxacin nor gatifloxacin were associated with increased odds of developing a dysglycemic event compared with azithromycin. Multivariate analysis demonstrated that lack of downward dosage adjustment based on creatinine clearance (odds ratio [OR] 10.3, 95% confidence interval [CI] 3.8–27.6), presence of diabetes (OR 17.1, 95% CI 3.1–94.9), or treatment with insulin (OR 5.3, 95% CI 1.8–15.7) or sulfonylureas (OR 3.6, 95% CI 1.3–10.4) independently increased dysglycemia risk. Obesity (body mass index &gt; 30 kg/m2) was independently protective (OR 0.22, 95% CI 0.09‐0.55) against dysglycemic events. Conclusion. Levofloxacin and gatifloxacin were not significantly associated with increased dysglycemic events compared with azithromycin. Lack of downward fluoroquinolone dosage adjustment for renal function, presence of diabetes, and treatment with insulin or sulfonylureas each independently increased the risk of dysglycemia. Obesity was independently protective against dysglycemia. More data are needed on the contributing effects of diabetes, fluoroquinolone dosage, and concomitant drug therapy so that an appropriate risk‐management strategy can be developed.</description><subject>Administration, Oral</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aminoacid disorders</subject><subject>Anti-Bacterial Agents - administration &amp; dosage</subject><subject>Anti-Bacterial Agents - adverse effects</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>azithromycin</subject><subject>Azithromycin - administration &amp; dosage</subject><subject>Azithromycin - adverse effects</subject><subject>Azithromycin - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Creatinine - blood</subject><subject>Diabetes Complications - drug therapy</subject><subject>dysglycemias</subject><subject>Errors of metabolism</subject><subject>Female</subject><subject>Fluoroquinolones - administration &amp; dosage</subject><subject>Fluoroquinolones - adverse effects</subject><subject>Fluoroquinolones - chemistry</subject><subject>Fluoroquinolones - therapeutic use</subject><subject>gatifloxacin</subject><subject>Hospitals, Veterans - statistics &amp; numerical data</subject><subject>Humans</subject><subject>hyperglycemia</subject><subject>Hyperglycemia - chemically induced</subject><subject>Hyperglycemia - epidemiology</subject><subject>hypoglycemia</subject><subject>Hypoglycemia - chemically induced</subject><subject>Hypoglycemia - epidemiology</subject><subject>Levofloxacin</subject><subject>Male</subject><subject>Medical Records - statistics &amp; numerical data</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Ofloxacin - administration &amp; dosage</subject><subject>Ofloxacin - adverse effects</subject><subject>Ofloxacin - therapeutic use</subject><subject>outpatient</subject><subject>Pharmacology. Drug treatments</subject><subject>Prevalence</subject><subject>Retrospective Studies</subject><subject>Rhode Island - epidemiology</subject><subject>Risk Factors</subject><issn>0277-0008</issn><issn>1875-9114</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp9kE1PwkAQhjdGI4jePJu9eLO4Hy2dPRoUMCGBoJ6bZXcWV0tLugUl_nmLEL15muSd551JHkIuOevyRInb1aspuwK6vAviiLQ5pEmkOI-PSZuJNI0YY9AiZyG8MSZ4LxanpMWBJ3GcQpt8TSvc6BwLg7R0VBeWznx4pwNt6rIK1JUVvd-GRb41uPSa-oJOde2xqAOdoUG_8cWCDpvI5eWnNs1-d2OMm_I3-MnoZF2v9k36hHXd1M7JidN5wIvD7JCXwcNzfxSNJ8PH_t04MrLH48hpi3bes86IWKWWgbQKdGrAKjRGzJVQUggQoLhIY8Osk4xbkHPUKCCRskNu9ndNVYZQoctWlV_qaptxlu0cZjuHmYCMZyAa_GqPr9bzJdo_-CCtAa4PgA5G567ShfHhj1MKGtVJw_E99-Fz3P77NJuO7mYSYvkNs_yMTA</recordid><startdate>200801</startdate><enddate>200801</enddate><creator>LaPlante, Kerry L.</creator><creator>Mersfelder, Tracey L.</creator><creator>Ward, Kristina E.</creator><creator>Quilliam, Brian J.</creator><general>Blackwell Publishing Ltd</general><general>Pharmacotherapy</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200801</creationdate><title>Prevalence of and Risk Factors for Dysglycemia in Patients Receiving Gatifloxacin and Levofloxacin in an Outpatient Setting</title><author>LaPlante, Kerry L. ; Mersfelder, Tracey L. ; Ward, Kristina E. ; Quilliam, Brian J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3614-fadedb6dfc2497d083d98a7c8d9ecc2b92932282891274c0df301d83beae28533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Administration, Oral</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aminoacid disorders</topic><topic>Anti-Bacterial Agents - administration &amp; dosage</topic><topic>Anti-Bacterial Agents - adverse effects</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>azithromycin</topic><topic>Azithromycin - administration &amp; dosage</topic><topic>Azithromycin - adverse effects</topic><topic>Azithromycin - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Creatinine - blood</topic><topic>Diabetes Complications - drug therapy</topic><topic>dysglycemias</topic><topic>Errors of metabolism</topic><topic>Female</topic><topic>Fluoroquinolones - administration &amp; dosage</topic><topic>Fluoroquinolones - adverse effects</topic><topic>Fluoroquinolones - chemistry</topic><topic>Fluoroquinolones - therapeutic use</topic><topic>gatifloxacin</topic><topic>Hospitals, Veterans - statistics &amp; numerical data</topic><topic>Humans</topic><topic>hyperglycemia</topic><topic>Hyperglycemia - chemically induced</topic><topic>Hyperglycemia - epidemiology</topic><topic>hypoglycemia</topic><topic>Hypoglycemia - chemically induced</topic><topic>Hypoglycemia - epidemiology</topic><topic>Levofloxacin</topic><topic>Male</topic><topic>Medical Records - statistics &amp; numerical data</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Ofloxacin - administration &amp; dosage</topic><topic>Ofloxacin - adverse effects</topic><topic>Ofloxacin - therapeutic use</topic><topic>outpatient</topic><topic>Pharmacology. Drug treatments</topic><topic>Prevalence</topic><topic>Retrospective Studies</topic><topic>Rhode Island - epidemiology</topic><topic>Risk Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LaPlante, Kerry L.</creatorcontrib><creatorcontrib>Mersfelder, Tracey L.</creatorcontrib><creatorcontrib>Ward, Kristina E.</creatorcontrib><creatorcontrib>Quilliam, Brian J.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Pharmacotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LaPlante, Kerry L.</au><au>Mersfelder, Tracey L.</au><au>Ward, Kristina E.</au><au>Quilliam, Brian J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevalence of and Risk Factors for Dysglycemia in Patients Receiving Gatifloxacin and Levofloxacin in an Outpatient Setting</atitle><jtitle>Pharmacotherapy</jtitle><addtitle>Pharmacotherapy</addtitle><date>2008-01</date><risdate>2008</risdate><volume>28</volume><issue>1</issue><spage>82</spage><epage>89</epage><pages>82-89</pages><issn>0277-0008</issn><eissn>1875-9114</eissn><coden>PHPYDQ</coden><abstract>Study Objectives. To assess the prevalence of dysglycemia (hypoglycemia or hyperglycemia) associated with oral levofloxacin and gatifloxacin therapy in an outpatient setting, and to determine the characteristics of patients who developed dysglycemia while receiving either fluoroquinolone. Design. Retrospective medical record review. Setting. Outpatient clinic of a Veterans Affairs teaching hospital. Patients. A total of 1573 patients who received oral levofloxacin (343 patients), gatifloxacin (589 patients), or azithromycin (as a control, 641 patients) between June 1, 2004, and May 31, 2006. Measurements and Main Results. Dysglycemia occurred in 33 patients: 13 (2.2%), 9 (2.6%), and 11 (1.7%), respectively, of those in the gatifloxacin, levofloxacin, and azithromycin groups. Of 13 patients who experienced a hyperglycemic event, 11 (84.6%) had diabetes mellitus. After adjustment for confounding factors, neither levofloxacin nor gatifloxacin were associated with increased odds of developing a dysglycemic event compared with azithromycin. Multivariate analysis demonstrated that lack of downward dosage adjustment based on creatinine clearance (odds ratio [OR] 10.3, 95% confidence interval [CI] 3.8–27.6), presence of diabetes (OR 17.1, 95% CI 3.1–94.9), or treatment with insulin (OR 5.3, 95% CI 1.8–15.7) or sulfonylureas (OR 3.6, 95% CI 1.3–10.4) independently increased dysglycemia risk. Obesity (body mass index &gt; 30 kg/m2) was independently protective (OR 0.22, 95% CI 0.09‐0.55) against dysglycemic events. Conclusion. Levofloxacin and gatifloxacin were not significantly associated with increased dysglycemic events compared with azithromycin. Lack of downward fluoroquinolone dosage adjustment for renal function, presence of diabetes, and treatment with insulin or sulfonylureas each independently increased the risk of dysglycemia. Obesity was independently protective against dysglycemia. More data are needed on the contributing effects of diabetes, fluoroquinolone dosage, and concomitant drug therapy so that an appropriate risk‐management strategy can be developed.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>18154478</pmid><doi>10.1592/phco.28.1.82</doi><tpages>8</tpages></addata></record>
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subjects Administration, Oral
Adult
Aged
Aged, 80 and over
Aminoacid disorders
Anti-Bacterial Agents - administration & dosage
Anti-Bacterial Agents - adverse effects
Anti-Bacterial Agents - therapeutic use
azithromycin
Azithromycin - administration & dosage
Azithromycin - adverse effects
Azithromycin - therapeutic use
Biological and medical sciences
Creatinine - blood
Diabetes Complications - drug therapy
dysglycemias
Errors of metabolism
Female
Fluoroquinolones - administration & dosage
Fluoroquinolones - adverse effects
Fluoroquinolones - chemistry
Fluoroquinolones - therapeutic use
gatifloxacin
Hospitals, Veterans - statistics & numerical data
Humans
hyperglycemia
Hyperglycemia - chemically induced
Hyperglycemia - epidemiology
hypoglycemia
Hypoglycemia - chemically induced
Hypoglycemia - epidemiology
Levofloxacin
Male
Medical Records - statistics & numerical data
Medical sciences
Metabolic diseases
Middle Aged
Multivariate Analysis
Ofloxacin - administration & dosage
Ofloxacin - adverse effects
Ofloxacin - therapeutic use
outpatient
Pharmacology. Drug treatments
Prevalence
Retrospective Studies
Rhode Island - epidemiology
Risk Factors
title Prevalence of and Risk Factors for Dysglycemia in Patients Receiving Gatifloxacin and Levofloxacin in an Outpatient Setting
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