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State of the art in cystic fibrosis pharmacology—Optimization of antimicrobials in the treatment of cystic fibrosis pulmonary exacerbations: I. Anti‐methicillin‐resistant Staphylococcus aureus (MRSA) antibiotics
Acute pulmonary exacerbations (APE) are a complication of cystic fibrosis (CF) and are associated with morbidity and mortality. Methicillin‐resistant Staphylococcus aureus (MRSA) is one of many organisms that has been detected in the airways of patients with CF. This review provides an evidence‐base...
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Published in: | Pediatric pulmonology 2020-01, Vol.55 (1), p.33-57 |
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description | Acute pulmonary exacerbations (APE) are a complication of cystic fibrosis (CF) and are associated with morbidity and mortality. Methicillin‐resistant Staphylococcus aureus (MRSA) is one of many organisms that has been detected in the airways of patients with CF. This review provides an evidence‐based summary of pharmacokinetic/pharmacodynamic (PK/PD), tolerability, and efficacy studies utilizing anti‐MRSA antibiotics (ie, ceftaroline, clindamycin, fluoroquinolone derivatives (ciprofloxacin, levofloxacin), glycopeptide derivatives (telavancin, vancomycin), linezolid, rifampin, sulfamethoxazole/trimethoprim (SMZ/TMP), and tetracycline derivatives (doxycycline, minocycline, tigecycline) in the treatment of APE and identifies areas where further study is warranted. A recent utilization study of antimicrobials for anti‐MRSA has shown some CF Foundation accredited care centers and affiliate programs are using doses higher than the FDA‐approved doses. Further studies are needed to determine the PK/PD properties in CF patients with clindamycin, minocycline, rifampin, SMZ/TMP, telavancin, and tigecycline; as well as, efficacy and tolerability studies with ciprofloxacin, clindamycin, doxycycline, levofloxacin, minocycline, rifampin, SMZ/TMP, in CF patients with MRSA. |
doi_str_mv | 10.1002/ppul.24537 |
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Further studies are needed to determine the PK/PD properties in CF patients with clindamycin, minocycline, rifampin, SMZ/TMP, telavancin, and tigecycline; as well as, efficacy and tolerability studies with ciprofloxacin, clindamycin, doxycycline, levofloxacin, minocycline, rifampin, SMZ/TMP, in CF patients with MRSA.</description><identifier>ISSN: 8755-6863</identifier><identifier>EISSN: 1099-0496</identifier><identifier>DOI: 10.1002/ppul.24537</identifier><identifier>PMID: 31609097</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Aminoglycosides ; Anti-Bacterial Agents - therapeutic use ; antibiotic therapy ; Antibiotics ; Ceftaroline ; Cephalosporins ; Ciprofloxacin ; Clindamycin ; Cystic fibrosis ; Cystic Fibrosis - drug therapy ; Humans ; Linezolid ; Lipoglycopeptides ; Methicillin ; Methicillin-Resistant Staphylococcus aureus - drug effects ; MRSA ; pharmacology ; Rifampin - therapeutic use ; Staphylococcus infections ; Trimethoprim, Sulfamethoxazole Drug Combination - therapeutic use ; Vancomycin - therapeutic use</subject><ispartof>Pediatric pulmonology, 2020-01, Vol.55 (1), p.33-57</ispartof><rights>2019 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3577-2274202143ba3ab9bd61e1c61c14658e438af964f927a6535fd9ac39dbaab9893</citedby><cites>FETCH-LOGICAL-c3577-2274202143ba3ab9bd61e1c61c14658e438af964f927a6535fd9ac39dbaab9893</cites><orcidid>0000-0001-6047-306X ; 0000-0003-0977-7257</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31609097$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Epps, Quovadis J.</creatorcontrib><creatorcontrib>Epps, Kevin L.</creatorcontrib><creatorcontrib>Young, David C.</creatorcontrib><creatorcontrib>Zobell, Jeffery T.</creatorcontrib><title>State of the art in cystic fibrosis pharmacology—Optimization of antimicrobials in the treatment of cystic fibrosis pulmonary exacerbations: I. Anti‐methicillin‐resistant Staphylococcus aureus (MRSA) antibiotics</title><title>Pediatric pulmonology</title><addtitle>Pediatr Pulmonol</addtitle><description>Acute pulmonary exacerbations (APE) are a complication of cystic fibrosis (CF) and are associated with morbidity and mortality. Methicillin‐resistant Staphylococcus aureus (MRSA) is one of many organisms that has been detected in the airways of patients with CF. This review provides an evidence‐based summary of pharmacokinetic/pharmacodynamic (PK/PD), tolerability, and efficacy studies utilizing anti‐MRSA antibiotics (ie, ceftaroline, clindamycin, fluoroquinolone derivatives (ciprofloxacin, levofloxacin), glycopeptide derivatives (telavancin, vancomycin), linezolid, rifampin, sulfamethoxazole/trimethoprim (SMZ/TMP), and tetracycline derivatives (doxycycline, minocycline, tigecycline) in the treatment of APE and identifies areas where further study is warranted. A recent utilization study of antimicrobials for anti‐MRSA has shown some CF Foundation accredited care centers and affiliate programs are using doses higher than the FDA‐approved doses. 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Anti‐methicillin‐resistant Staphylococcus aureus (MRSA) antibiotics</title><author>Epps, Quovadis J. ; Epps, Kevin L. ; Young, David C. ; Zobell, Jeffery T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3577-2274202143ba3ab9bd61e1c61c14658e438af964f927a6535fd9ac39dbaab9893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aminoglycosides</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>antibiotic therapy</topic><topic>Antibiotics</topic><topic>Ceftaroline</topic><topic>Cephalosporins</topic><topic>Ciprofloxacin</topic><topic>Clindamycin</topic><topic>Cystic fibrosis</topic><topic>Cystic Fibrosis - drug therapy</topic><topic>Humans</topic><topic>Linezolid</topic><topic>Lipoglycopeptides</topic><topic>Methicillin</topic><topic>Methicillin-Resistant Staphylococcus aureus - drug effects</topic><topic>MRSA</topic><topic>pharmacology</topic><topic>Rifampin - therapeutic use</topic><topic>Staphylococcus infections</topic><topic>Trimethoprim, Sulfamethoxazole Drug Combination - therapeutic use</topic><topic>Vancomycin - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Epps, Quovadis J.</creatorcontrib><creatorcontrib>Epps, Kevin L.</creatorcontrib><creatorcontrib>Young, David C.</creatorcontrib><creatorcontrib>Zobell, Jeffery T.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric pulmonology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Epps, Quovadis J.</au><au>Epps, Kevin L.</au><au>Young, David C.</au><au>Zobell, Jeffery T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>State of the art in cystic fibrosis pharmacology—Optimization of antimicrobials in the treatment of cystic fibrosis pulmonary exacerbations: I. Anti‐methicillin‐resistant Staphylococcus aureus (MRSA) antibiotics</atitle><jtitle>Pediatric pulmonology</jtitle><addtitle>Pediatr Pulmonol</addtitle><date>2020-01</date><risdate>2020</risdate><volume>55</volume><issue>1</issue><spage>33</spage><epage>57</epage><pages>33-57</pages><issn>8755-6863</issn><eissn>1099-0496</eissn><abstract>Acute pulmonary exacerbations (APE) are a complication of cystic fibrosis (CF) and are associated with morbidity and mortality. Methicillin‐resistant Staphylococcus aureus (MRSA) is one of many organisms that has been detected in the airways of patients with CF. 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Further studies are needed to determine the PK/PD properties in CF patients with clindamycin, minocycline, rifampin, SMZ/TMP, telavancin, and tigecycline; as well as, efficacy and tolerability studies with ciprofloxacin, clindamycin, doxycycline, levofloxacin, minocycline, rifampin, SMZ/TMP, in CF patients with MRSA.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31609097</pmid><doi>10.1002/ppul.24537</doi><tpages>25</tpages><orcidid>https://orcid.org/0000-0001-6047-306X</orcidid><orcidid>https://orcid.org/0000-0003-0977-7257</orcidid></addata></record> |
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subjects | Aminoglycosides Anti-Bacterial Agents - therapeutic use antibiotic therapy Antibiotics Ceftaroline Cephalosporins Ciprofloxacin Clindamycin Cystic fibrosis Cystic Fibrosis - drug therapy Humans Linezolid Lipoglycopeptides Methicillin Methicillin-Resistant Staphylococcus aureus - drug effects MRSA pharmacology Rifampin - therapeutic use Staphylococcus infections Trimethoprim, Sulfamethoxazole Drug Combination - therapeutic use Vancomycin - therapeutic use |
title | State of the art in cystic fibrosis pharmacology—Optimization of antimicrobials in the treatment of cystic fibrosis pulmonary exacerbations: I. Anti‐methicillin‐resistant Staphylococcus aureus (MRSA) antibiotics |
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