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Implementation of safety standards of compounded sterile preparations in hospital pharmacies: a multinational cross-sectional study

ObjectivesTo evaluate implementation of safety standards of compounded sterile preparations in different hospitals.MethodsThis cross-sectional study included 124 hospitals from 19 countries. A survey was developed based on the guidelines and safety practices of the Institute for Safe Medication Prac...

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Published in:European journal of hospital pharmacy. Science and practice 2016-11, Vol.23 (6), p.339-342
Main Authors: Al-Fadel, Nouf, Mahmoud, Mansour A, Dabliz, Rabih, Tabbara, Osama, Aljadhey, Hisham
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cited_by cdi_FETCH-LOGICAL-b476t-9a606656320074f23511a088508edc34acfceda5b96b4f22a47cea2a1fc635a73
cites cdi_FETCH-LOGICAL-b476t-9a606656320074f23511a088508edc34acfceda5b96b4f22a47cea2a1fc635a73
container_end_page 342
container_issue 6
container_start_page 339
container_title European journal of hospital pharmacy. Science and practice
container_volume 23
creator Al-Fadel, Nouf
Mahmoud, Mansour A
Dabliz, Rabih
Tabbara, Osama
Aljadhey, Hisham
description ObjectivesTo evaluate implementation of safety standards of compounded sterile preparations in different hospitals.MethodsThis cross-sectional study included 124 hospitals from 19 countries. A survey was developed based on the guidelines and safety practices of the Institute for Safe Medication Practices (ISMP) for sterile preparations compounding, and was sent to the members of the Intravenous and Parenteral Nutrition experts’ network (IV PN experts’ network) in the Gulf region and beyond using SurveyMonkey software.Results124 pharmacists were invited to participate in this study. Only 39 (31.5%) pharmacists from seven countries responded: 16 (41%) of the participants were pharmacy supervisors, and 23 (59%) had >10 years of work experience. However, a majority, 27 (69%), of the respondents were from Saudi Arabia. Written policies and procedures for sterile preparations compounding were available in 37 (95%) hospitals. The concentrated electrolytes were removed from all patient care areas in 28 (72%) hospitals, and 30 (77%) hospitals clearly labelled those as high-alert medications. The use of advanced technologies, such as bar code verification or IV robotics, for compounding sterile preparations were not implemented in 27 (69%) hospitals.ConclusionsMinimum standards and best practice recommendations to ensure safety of sterile preparation compounding were implemented in many hospitals of different countries. However, advanced technologies were not implemented by the majority of the hospitals.
doi_str_mv 10.1136/ejhpharm-2015-000872
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A survey was developed based on the guidelines and safety practices of the Institute for Safe Medication Practices (ISMP) for sterile preparations compounding, and was sent to the members of the Intravenous and Parenteral Nutrition experts’ network (IV PN experts’ network) in the Gulf region and beyond using SurveyMonkey software.Results124 pharmacists were invited to participate in this study. Only 39 (31.5%) pharmacists from seven countries responded: 16 (41%) of the participants were pharmacy supervisors, and 23 (59%) had &gt;10 years of work experience. However, a majority, 27 (69%), of the respondents were from Saudi Arabia. Written policies and procedures for sterile preparations compounding were available in 37 (95%) hospitals. The concentrated electrolytes were removed from all patient care areas in 28 (72%) hospitals, and 30 (77%) hospitals clearly labelled those as high-alert medications. The use of advanced technologies, such as bar code verification or IV robotics, for compounding sterile preparations were not implemented in 27 (69%) hospitals.ConclusionsMinimum standards and best practice recommendations to ensure safety of sterile preparation compounding were implemented in many hospitals of different countries. However, advanced technologies were not implemented by the majority of the hospitals.</description><identifier>ISSN: 2047-9956</identifier><identifier>EISSN: 2047-9964</identifier><identifier>DOI: 10.1136/ejhpharm-2015-000872</identifier><identifier>PMID: 31156879</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><subject>Automation ; Drug stores ; Electrolytes ; Medical errors ; Original ; Patient safety ; Pharmacists ; Safety standards ; Studies</subject><ispartof>European journal of hospital pharmacy. Science and practice, 2016-11, Vol.23 (6), p.339-342</ispartof><rights>Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing</rights><rights>Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/2016</rights><rights>Published by the BMJ Publishing Group Limited. 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Science and practice</title><description>ObjectivesTo evaluate implementation of safety standards of compounded sterile preparations in different hospitals.MethodsThis cross-sectional study included 124 hospitals from 19 countries. A survey was developed based on the guidelines and safety practices of the Institute for Safe Medication Practices (ISMP) for sterile preparations compounding, and was sent to the members of the Intravenous and Parenteral Nutrition experts’ network (IV PN experts’ network) in the Gulf region and beyond using SurveyMonkey software.Results124 pharmacists were invited to participate in this study. Only 39 (31.5%) pharmacists from seven countries responded: 16 (41%) of the participants were pharmacy supervisors, and 23 (59%) had &gt;10 years of work experience. However, a majority, 27 (69%), of the respondents were from Saudi Arabia. Written policies and procedures for sterile preparations compounding were available in 37 (95%) hospitals. The concentrated electrolytes were removed from all patient care areas in 28 (72%) hospitals, and 30 (77%) hospitals clearly labelled those as high-alert medications. The use of advanced technologies, such as bar code verification or IV robotics, for compounding sterile preparations were not implemented in 27 (69%) hospitals.ConclusionsMinimum standards and best practice recommendations to ensure safety of sterile preparation compounding were implemented in many hospitals of different countries. 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Science and practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Al-Fadel, Nouf</au><au>Mahmoud, Mansour A</au><au>Dabliz, Rabih</au><au>Tabbara, Osama</au><au>Aljadhey, Hisham</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Implementation of safety standards of compounded sterile preparations in hospital pharmacies: a multinational cross-sectional study</atitle><jtitle>European journal of hospital pharmacy. Science and practice</jtitle><date>2016-11-01</date><risdate>2016</risdate><volume>23</volume><issue>6</issue><spage>339</spage><epage>342</epage><pages>339-342</pages><issn>2047-9956</issn><eissn>2047-9964</eissn><abstract>ObjectivesTo evaluate implementation of safety standards of compounded sterile preparations in different hospitals.MethodsThis cross-sectional study included 124 hospitals from 19 countries. A survey was developed based on the guidelines and safety practices of the Institute for Safe Medication Practices (ISMP) for sterile preparations compounding, and was sent to the members of the Intravenous and Parenteral Nutrition experts’ network (IV PN experts’ network) in the Gulf region and beyond using SurveyMonkey software.Results124 pharmacists were invited to participate in this study. Only 39 (31.5%) pharmacists from seven countries responded: 16 (41%) of the participants were pharmacy supervisors, and 23 (59%) had &gt;10 years of work experience. However, a majority, 27 (69%), of the respondents were from Saudi Arabia. Written policies and procedures for sterile preparations compounding were available in 37 (95%) hospitals. The concentrated electrolytes were removed from all patient care areas in 28 (72%) hospitals, and 30 (77%) hospitals clearly labelled those as high-alert medications. The use of advanced technologies, such as bar code verification or IV robotics, for compounding sterile preparations were not implemented in 27 (69%) hospitals.ConclusionsMinimum standards and best practice recommendations to ensure safety of sterile preparation compounding were implemented in many hospitals of different countries. However, advanced technologies were not implemented by the majority of the hospitals.</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><pmid>31156879</pmid><doi>10.1136/ejhpharm-2015-000872</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record>
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subjects Automation
Drug stores
Electrolytes
Medical errors
Original
Patient safety
Pharmacists
Safety standards
Studies
title Implementation of safety standards of compounded sterile preparations in hospital pharmacies: a multinational cross-sectional study
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