Identification of severe potential drug-drug interactions using an Italian general-practitioner database
Objective To analyze prescriptions in a general-practitioner database over 1 year to determine the frequency, the characteristics, and the monitoring of the severe potential drug-drug interactions (DDIs). Methods We retrospectively analyzed the clinical records from 16 general practitioners in the V...
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creator | Magro, L. Conforti, A. Del Zotti, F. Leone, R. Iorio, M. L. Meneghelli, I. Massignani, D. Visonà, E. Moretti, U. |
description | Objective
To analyze prescriptions in a general-practitioner database over 1 year to determine the frequency, the characteristics, and the monitoring of the severe potential drug-drug interactions (DDIs).
Methods
We retrospectively analyzed the clinical records from 16 general practitioners in the Veneto region, an area in northern Italy. The study covered the period from January 1 to December 31, 2004. We selected all severe and well-documented interactions according to the book
Drug Interaction Facts
by David S. Tatro (Facts and Comparisons, St. Louis, MO, 2006). We grouped severe potential DDIs according to their specific potential risk, and for the most frequently interacting drug pairs, we investigated whether some specific tests had been prescribed by physicians for safety monitoring.
Results
During the study period, 16,037 patients (55% female) with at least one drug prescription were recorded, and a total of 185,704 prescriptions relating to 1,020 different drugs were analyzed. Ramipril was the most frequently prescribed drug followed by acetylsalicylic acid and atorvastatin. The final number of different types of severe potential DDIs was 119, which occurred 1,037 times in 758 patients (4.7% of the total number of patients). More than 80% of drugs involved in severe potential DDIs were cardiovascular drugs. Digoxin was the most frequently involved drug. Electrolyte disturbances, increase in serum digoxin levels, risk of hemorrhage, severe myopathy or rhabdomyolysis, and cardiac arrhythmias were the most commonly implicated potential risks. When considering patients using digoxin with loop or thiazide diuretics for more than 5 months, 72% had at least one test to monitor potential digoxin toxicity, whereas 28% had no tests. Sixty-four percent of patients using digoxin with amiodarone, verapamil, or propafenone had an ECG and/or digoxin monitoring, and 36% of them did not have any tests.
Conclusions
The present study revealed that, in a group of Italian general practitioners, the risks of severe potential drug interactions are relatively low and the drugs concerned are few. Analyses of specific tests showed that physicians are generally aware of the potential risks caused by digoxin drug associations. However not all patients were closely monitored and this should be improved. |
doi_str_mv | 10.1007/s00228-007-0394-1 |
format | Article |
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To analyze prescriptions in a general-practitioner database over 1 year to determine the frequency, the characteristics, and the monitoring of the severe potential drug-drug interactions (DDIs).
Methods
We retrospectively analyzed the clinical records from 16 general practitioners in the Veneto region, an area in northern Italy. The study covered the period from January 1 to December 31, 2004. We selected all severe and well-documented interactions according to the book
Drug Interaction Facts
by David S. Tatro (Facts and Comparisons, St. Louis, MO, 2006). We grouped severe potential DDIs according to their specific potential risk, and for the most frequently interacting drug pairs, we investigated whether some specific tests had been prescribed by physicians for safety monitoring.
Results
During the study period, 16,037 patients (55% female) with at least one drug prescription were recorded, and a total of 185,704 prescriptions relating to 1,020 different drugs were analyzed. Ramipril was the most frequently prescribed drug followed by acetylsalicylic acid and atorvastatin. The final number of different types of severe potential DDIs was 119, which occurred 1,037 times in 758 patients (4.7% of the total number of patients). More than 80% of drugs involved in severe potential DDIs were cardiovascular drugs. Digoxin was the most frequently involved drug. Electrolyte disturbances, increase in serum digoxin levels, risk of hemorrhage, severe myopathy or rhabdomyolysis, and cardiac arrhythmias were the most commonly implicated potential risks. When considering patients using digoxin with loop or thiazide diuretics for more than 5 months, 72% had at least one test to monitor potential digoxin toxicity, whereas 28% had no tests. Sixty-four percent of patients using digoxin with amiodarone, verapamil, or propafenone had an ECG and/or digoxin monitoring, and 36% of them did not have any tests.
Conclusions
The present study revealed that, in a group of Italian general practitioners, the risks of severe potential drug interactions are relatively low and the drugs concerned are few. Analyses of specific tests showed that physicians are generally aware of the potential risks caused by digoxin drug associations. However not all patients were closely monitored and this should be improved.</description><identifier>ISSN: 0031-6970</identifier><identifier>EISSN: 1432-1041</identifier><identifier>DOI: 10.1007/s00228-007-0394-1</identifier><identifier>PMID: 17992523</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Adolescent ; Adult ; Adverse Drug Reaction Reporting Systems - statistics & numerical data ; Aged ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedicine ; Child ; Child, Preschool ; Data analysis ; Databases, Factual ; Drug Interactions ; Drug Monitoring - standards ; Drug Monitoring - statistics & numerical data ; Drug therapy ; Female ; Humans ; Infant ; Italy ; Male ; Medical sciences ; Middle Aged ; Pharmacoepidemiology and Prescription ; Pharmacology ; Pharmacology. Drug treatments ; Pharmacology/Toxicology ; Physicians ; Physicians, Family - standards ; Physicians, Family - statistics & numerical data ; Practice Patterns, Physicians' - standards ; Practice Patterns, Physicians' - statistics & numerical data ; Retrospective Studies ; Risk Factors</subject><ispartof>European journal of clinical pharmacology, 2008-03, Vol.64 (3), p.303-309</ispartof><rights>Springer-Verlag 2007</rights><rights>2008 INIST-CNRS</rights><rights>Springer-Verlag 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c399t-12e5446ef8e0570b0fa394e99be769c07efa7a66df67594284a990c595d14bac3</citedby><cites>FETCH-LOGICAL-c399t-12e5446ef8e0570b0fa394e99be769c07efa7a66df67594284a990c595d14bac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00228-007-0394-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00228-007-0394-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,782,786,27931,27932,41495,42564,51326</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20126589$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17992523$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Magro, L.</creatorcontrib><creatorcontrib>Conforti, A.</creatorcontrib><creatorcontrib>Del Zotti, F.</creatorcontrib><creatorcontrib>Leone, R.</creatorcontrib><creatorcontrib>Iorio, M. L.</creatorcontrib><creatorcontrib>Meneghelli, I.</creatorcontrib><creatorcontrib>Massignani, D.</creatorcontrib><creatorcontrib>Visonà, E.</creatorcontrib><creatorcontrib>Moretti, U.</creatorcontrib><title>Identification of severe potential drug-drug interactions using an Italian general-practitioner database</title><title>European journal of clinical pharmacology</title><addtitle>Eur J Clin Pharmacol</addtitle><addtitle>Eur J Clin Pharmacol</addtitle><description>Objective
To analyze prescriptions in a general-practitioner database over 1 year to determine the frequency, the characteristics, and the monitoring of the severe potential drug-drug interactions (DDIs).
Methods
We retrospectively analyzed the clinical records from 16 general practitioners in the Veneto region, an area in northern Italy. The study covered the period from January 1 to December 31, 2004. We selected all severe and well-documented interactions according to the book
Drug Interaction Facts
by David S. Tatro (Facts and Comparisons, St. Louis, MO, 2006). We grouped severe potential DDIs according to their specific potential risk, and for the most frequently interacting drug pairs, we investigated whether some specific tests had been prescribed by physicians for safety monitoring.
Results
During the study period, 16,037 patients (55% female) with at least one drug prescription were recorded, and a total of 185,704 prescriptions relating to 1,020 different drugs were analyzed. Ramipril was the most frequently prescribed drug followed by acetylsalicylic acid and atorvastatin. The final number of different types of severe potential DDIs was 119, which occurred 1,037 times in 758 patients (4.7% of the total number of patients). More than 80% of drugs involved in severe potential DDIs were cardiovascular drugs. Digoxin was the most frequently involved drug. Electrolyte disturbances, increase in serum digoxin levels, risk of hemorrhage, severe myopathy or rhabdomyolysis, and cardiac arrhythmias were the most commonly implicated potential risks. When considering patients using digoxin with loop or thiazide diuretics for more than 5 months, 72% had at least one test to monitor potential digoxin toxicity, whereas 28% had no tests. Sixty-four percent of patients using digoxin with amiodarone, verapamil, or propafenone had an ECG and/or digoxin monitoring, and 36% of them did not have any tests.
Conclusions
The present study revealed that, in a group of Italian general practitioners, the risks of severe potential drug interactions are relatively low and the drugs concerned are few. Analyses of specific tests showed that physicians are generally aware of the potential risks caused by digoxin drug associations. However not all patients were closely monitored and this should be improved.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Adverse Drug Reaction Reporting Systems - statistics & numerical data</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Data analysis</subject><subject>Databases, Factual</subject><subject>Drug Interactions</subject><subject>Drug Monitoring - standards</subject><subject>Drug Monitoring - statistics & numerical data</subject><subject>Drug therapy</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Italy</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacoepidemiology and Prescription</subject><subject>Pharmacology</subject><subject>Pharmacology. Drug treatments</subject><subject>Pharmacology/Toxicology</subject><subject>Physicians</subject><subject>Physicians, Family - standards</subject><subject>Physicians, Family - statistics & numerical data</subject><subject>Practice Patterns, Physicians' - standards</subject><subject>Practice Patterns, Physicians' - statistics & numerical data</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><issn>0031-6970</issn><issn>1432-1041</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kE1P3DAQhi1UBFvaH8AFWZV6dBk7dhwfEaLtSki9lHM0ccZLUHAWO6nUf4_Drsqpl5mR3me-XsYuJXyTAPY6AyjViFIKqJwW8oRtpK6UkKDlB7YBqKSonYVz9jHnJwBpHFRn7Fxa55RR1YY9bnuK8xAGj_MwRT4FnukPJeL7aV4VHHmflp1YAx_iTAn9Sma-5CHuOEa-nXEcSt5RLOoo9m_IClHiPc7YYaZP7DTgmOnzMV-wh-93v29_ivtfP7a3N_fCV87NQioyWtcUGgJjoYOA5TNyriNbOw-WAlqs6z7U1jitGo3OgTfO9FJ36KsL9uUwd5-ml4Xy3D5NS4plZauk1o3RzhZIHiCfppwThXafhmdMf1sJ7Wpte7C2XcvV2laWnqvj4KV7pv694-hlAb4eAcwex5Aw-iH_4xRIVZvGFU4duFykuKP0fuH_t78C4TSSGA</recordid><startdate>20080301</startdate><enddate>20080301</enddate><creator>Magro, L.</creator><creator>Conforti, A.</creator><creator>Del Zotti, F.</creator><creator>Leone, R.</creator><creator>Iorio, M. L.</creator><creator>Meneghelli, I.</creator><creator>Massignani, D.</creator><creator>Visonà, E.</creator><creator>Moretti, U.</creator><general>Springer-Verlag</general><general>Springer</general><general>Springer Nature B.V</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><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20080301</creationdate><title>Identification of severe potential drug-drug interactions using an Italian general-practitioner database</title><author>Magro, L. ; Conforti, A. ; Del Zotti, F. ; Leone, R. ; Iorio, M. L. ; Meneghelli, I. ; Massignani, D. ; Visonà, E. ; Moretti, U.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c399t-12e5446ef8e0570b0fa394e99be769c07efa7a66df67594284a990c595d14bac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Adverse Drug Reaction Reporting Systems - statistics & numerical data</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Data analysis</topic><topic>Databases, Factual</topic><topic>Drug Interactions</topic><topic>Drug Monitoring - standards</topic><topic>Drug Monitoring - statistics & numerical data</topic><topic>Drug therapy</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Italy</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacoepidemiology and Prescription</topic><topic>Pharmacology</topic><topic>Pharmacology. Drug treatments</topic><topic>Pharmacology/Toxicology</topic><topic>Physicians</topic><topic>Physicians, Family - standards</topic><topic>Physicians, Family - statistics & numerical data</topic><topic>Practice Patterns, Physicians' - standards</topic><topic>Practice Patterns, Physicians' - statistics & numerical data</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Magro, L.</creatorcontrib><creatorcontrib>Conforti, A.</creatorcontrib><creatorcontrib>Del Zotti, F.</creatorcontrib><creatorcontrib>Leone, R.</creatorcontrib><creatorcontrib>Iorio, M. L.</creatorcontrib><creatorcontrib>Meneghelli, I.</creatorcontrib><creatorcontrib>Massignani, D.</creatorcontrib><creatorcontrib>Visonà, E.</creatorcontrib><creatorcontrib>Moretti, U.</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><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>European journal of clinical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Magro, L.</au><au>Conforti, A.</au><au>Del Zotti, F.</au><au>Leone, R.</au><au>Iorio, M. L.</au><au>Meneghelli, I.</au><au>Massignani, D.</au><au>Visonà, E.</au><au>Moretti, U.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of severe potential drug-drug interactions using an Italian general-practitioner database</atitle><jtitle>European journal of clinical pharmacology</jtitle><stitle>Eur J Clin Pharmacol</stitle><addtitle>Eur J Clin Pharmacol</addtitle><date>2008-03-01</date><risdate>2008</risdate><volume>64</volume><issue>3</issue><spage>303</spage><epage>309</epage><pages>303-309</pages><issn>0031-6970</issn><eissn>1432-1041</eissn><abstract>Objective
To analyze prescriptions in a general-practitioner database over 1 year to determine the frequency, the characteristics, and the monitoring of the severe potential drug-drug interactions (DDIs).
Methods
We retrospectively analyzed the clinical records from 16 general practitioners in the Veneto region, an area in northern Italy. The study covered the period from January 1 to December 31, 2004. We selected all severe and well-documented interactions according to the book
Drug Interaction Facts
by David S. Tatro (Facts and Comparisons, St. Louis, MO, 2006). We grouped severe potential DDIs according to their specific potential risk, and for the most frequently interacting drug pairs, we investigated whether some specific tests had been prescribed by physicians for safety monitoring.
Results
During the study period, 16,037 patients (55% female) with at least one drug prescription were recorded, and a total of 185,704 prescriptions relating to 1,020 different drugs were analyzed. Ramipril was the most frequently prescribed drug followed by acetylsalicylic acid and atorvastatin. The final number of different types of severe potential DDIs was 119, which occurred 1,037 times in 758 patients (4.7% of the total number of patients). More than 80% of drugs involved in severe potential DDIs were cardiovascular drugs. Digoxin was the most frequently involved drug. Electrolyte disturbances, increase in serum digoxin levels, risk of hemorrhage, severe myopathy or rhabdomyolysis, and cardiac arrhythmias were the most commonly implicated potential risks. When considering patients using digoxin with loop or thiazide diuretics for more than 5 months, 72% had at least one test to monitor potential digoxin toxicity, whereas 28% had no tests. Sixty-four percent of patients using digoxin with amiodarone, verapamil, or propafenone had an ECG and/or digoxin monitoring, and 36% of them did not have any tests.
Conclusions
The present study revealed that, in a group of Italian general practitioners, the risks of severe potential drug interactions are relatively low and the drugs concerned are few. Analyses of specific tests showed that physicians are generally aware of the potential risks caused by digoxin drug associations. However not all patients were closely monitored and this should be improved.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>17992523</pmid><doi>10.1007/s00228-007-0394-1</doi><tpages>7</tpages></addata></record> |
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subjects | Adolescent Adult Adverse Drug Reaction Reporting Systems - statistics & numerical data Aged Biological and medical sciences Biomedical and Life Sciences Biomedicine Child Child, Preschool Data analysis Databases, Factual Drug Interactions Drug Monitoring - standards Drug Monitoring - statistics & numerical data Drug therapy Female Humans Infant Italy Male Medical sciences Middle Aged Pharmacoepidemiology and Prescription Pharmacology Pharmacology. Drug treatments Pharmacology/Toxicology Physicians Physicians, Family - standards Physicians, Family - statistics & numerical data Practice Patterns, Physicians' - standards Practice Patterns, Physicians' - statistics & numerical data Retrospective Studies Risk Factors |
title | Identification of severe potential drug-drug interactions using an Italian general-practitioner database |
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