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Indomethacin Pharmacodynamics Are Altered by Surfactant: A Possible Challenge to Current Indomethacin Dosing Guidelines Created Before Surfactant Availability
The effect of surfactant administration for respiratory distress syndrome (RDS) on indomethacin (INDO) pharmacodynamics and dosing requirements for patent ductus arteriosus (PDA) closure and renal toxicity was evaluated. A 22-year prospective cohort study including 442 INDO-treated patients given 46...
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Published in: | Pediatric cardiology 2010-05, Vol.31 (4), p.505-510 |
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creator | McPherson, Christopher Gal, Peter Ransom, J. Laurence Carlos, Rita Q. Dimaguila, Mary Ann V. T. Smith, McCrae Davonzo, Christie Wimmer, John E. |
description | The effect of surfactant administration for respiratory distress syndrome (RDS) on indomethacin (INDO) pharmacodynamics and dosing requirements for patent ductus arteriosus (PDA) closure and renal toxicity was evaluated. A 22-year prospective cohort study including 442 INDO-treated patients given 466 INDO treatment courses. The database included demographic information, medical problems, and medications. Neonates with a PDA confirmed by echocardiography were treated with INDO, 0.25–0.3 mg/kg. Subsequent INDO dosing was based on a combined pharmacokinetic/pharmacodynamic (PK/PD) approach. Data were fit to an Emax model and ANOVA was used to compare mean closure levels between groups. PDA closure was successful in 405 of 442 patients (91.6%) and in 434 of 466 treatment courses (93.1%) using an individualized PK/PD dosing approach. Renal toxicity was documented in 56 of 442 patients (12.7%) or 56 of 466 treatment courses (12.0%). Patients not treated with synthetic surfactant trended toward lower mean INDO concentrations at PDA closure compared to patients treated with synthetic surfactant (1.65 vs. 2.01 mg/l;
P
> 0.05) and significantly lower mean INDO concentrations at PDA closure compared to patients treated with natural surfactant (1.65 vs. 2.15 mg/l;
P
|
doi_str_mv | 10.1007/s00246-009-9628-6 |
format | article |
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P
> 0.05) and significantly lower mean INDO concentrations at PDA closure compared to patients treated with natural surfactant (1.65 vs. 2.15 mg/l;
P
< 0.002). This requires an increased total dose of ~0.3 mg/kg or an individual dose increase of 0.1 mg/kg. Administration of natural or synthetic surfactant for RDS may increase the INDO concentrations and doses needed for PDA closure in premature infants.</description><identifier>ISSN: 0172-0643</identifier><identifier>EISSN: 1432-1971</identifier><identifier>DOI: 10.1007/s00246-009-9628-6</identifier><identifier>PMID: 20063159</identifier><language>eng</language><publisher>New York: Springer-Verlag</publisher><subject><![CDATA[Analysis ; Animals ; Anti-Inflammatory Agents, Non-Steroidal - administration & dosage ; Anti-Inflammatory Agents, Non-Steroidal - pharmacokinetics ; Anti-Inflammatory Agents, Non-Steroidal - toxicity ; Biological Availability ; Biological Products - administration & dosage ; Calfactant ; Cardiac Surgery ; Cardiology ; Care and treatment ; Cohort Studies ; Congenital heart disease ; Dose-Response Relationship, Drug ; Drug Administration Schedule ; Drug Combinations ; Drug Interactions ; Ductus Arteriosus, Patent - blood ; Ductus Arteriosus, Patent - diagnostic imaging ; Ductus Arteriosus, Patent - drug therapy ; Echocardiography ; Echocardiography, Doppler, Color ; Fatty Alcohols - administration & dosage ; Guideline Adherence ; Humans ; Indomethacin ; Indomethacin - administration & dosage ; Indomethacin - pharmacokinetics ; Indomethacin - toxicity ; Infant, Newborn ; Intensive Care Units, Neonatal ; Kidney - drug effects ; Medical research ; Medicine ; Medicine & Public Health ; Medicine, Experimental ; Metabolic Clearance Rate ; Neonatology ; Original Article ; Phosphorylcholine - administration & dosage ; Polyethylene Glycols - administration & dosage ; Prospective Studies ; Pulmonary Surfactants - administration & dosage ; Respiratory Distress Syndrome, Newborn - blood ; Respiratory Distress Syndrome, Newborn - diagnostic imaging ; Respiratory Distress Syndrome, Newborn - drug therapy ; Vascular Surgery]]></subject><ispartof>Pediatric cardiology, 2010-05, Vol.31 (4), p.505-510</ispartof><rights>Springer Science+Business Media, LLC 2010</rights><rights>COPYRIGHT 2010 Springer</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c453t-f090cc5e3d1645957871f3335cde9b838dd4343a969fd83794365520a37ba95a3</citedby><cites>FETCH-LOGICAL-c453t-f090cc5e3d1645957871f3335cde9b838dd4343a969fd83794365520a37ba95a3</cites></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/20063159$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>McPherson, Christopher</creatorcontrib><creatorcontrib>Gal, Peter</creatorcontrib><creatorcontrib>Ransom, J. Laurence</creatorcontrib><creatorcontrib>Carlos, Rita Q.</creatorcontrib><creatorcontrib>Dimaguila, Mary Ann V. T.</creatorcontrib><creatorcontrib>Smith, McCrae</creatorcontrib><creatorcontrib>Davonzo, Christie</creatorcontrib><creatorcontrib>Wimmer, John E.</creatorcontrib><title>Indomethacin Pharmacodynamics Are Altered by Surfactant: A Possible Challenge to Current Indomethacin Dosing Guidelines Created Before Surfactant Availability</title><title>Pediatric cardiology</title><addtitle>Pediatr Cardiol</addtitle><addtitle>Pediatr Cardiol</addtitle><description>The effect of surfactant administration for respiratory distress syndrome (RDS) on indomethacin (INDO) pharmacodynamics and dosing requirements for patent ductus arteriosus (PDA) closure and renal toxicity was evaluated. A 22-year prospective cohort study including 442 INDO-treated patients given 466 INDO treatment courses. The database included demographic information, medical problems, and medications. Neonates with a PDA confirmed by echocardiography were treated with INDO, 0.25–0.3 mg/kg. Subsequent INDO dosing was based on a combined pharmacokinetic/pharmacodynamic (PK/PD) approach. Data were fit to an Emax model and ANOVA was used to compare mean closure levels between groups. PDA closure was successful in 405 of 442 patients (91.6%) and in 434 of 466 treatment courses (93.1%) using an individualized PK/PD dosing approach. Renal toxicity was documented in 56 of 442 patients (12.7%) or 56 of 466 treatment courses (12.0%). Patients not treated with synthetic surfactant trended toward lower mean INDO concentrations at PDA closure compared to patients treated with synthetic surfactant (1.65 vs. 2.01 mg/l;
P
> 0.05) and significantly lower mean INDO concentrations at PDA closure compared to patients treated with natural surfactant (1.65 vs. 2.15 mg/l;
P
< 0.002). This requires an increased total dose of ~0.3 mg/kg or an individual dose increase of 0.1 mg/kg. Administration of natural or synthetic surfactant for RDS may increase the INDO concentrations and doses needed for PDA closure in premature infants.</description><subject>Analysis</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - pharmacokinetics</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - toxicity</subject><subject>Biological Availability</subject><subject>Biological Products - administration & dosage</subject><subject>Calfactant</subject><subject>Cardiac Surgery</subject><subject>Cardiology</subject><subject>Care and treatment</subject><subject>Cohort Studies</subject><subject>Congenital heart disease</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Administration Schedule</subject><subject>Drug Combinations</subject><subject>Drug Interactions</subject><subject>Ductus Arteriosus, Patent - blood</subject><subject>Ductus Arteriosus, Patent - diagnostic imaging</subject><subject>Ductus Arteriosus, Patent - drug therapy</subject><subject>Echocardiography</subject><subject>Echocardiography, Doppler, Color</subject><subject>Fatty Alcohols - administration & dosage</subject><subject>Guideline Adherence</subject><subject>Humans</subject><subject>Indomethacin</subject><subject>Indomethacin - administration & dosage</subject><subject>Indomethacin - pharmacokinetics</subject><subject>Indomethacin - toxicity</subject><subject>Infant, Newborn</subject><subject>Intensive Care Units, Neonatal</subject><subject>Kidney - drug effects</subject><subject>Medical research</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Medicine, Experimental</subject><subject>Metabolic Clearance Rate</subject><subject>Neonatology</subject><subject>Original Article</subject><subject>Phosphorylcholine - administration & dosage</subject><subject>Polyethylene Glycols - administration & dosage</subject><subject>Prospective Studies</subject><subject>Pulmonary Surfactants - administration & dosage</subject><subject>Respiratory Distress Syndrome, Newborn - blood</subject><subject>Respiratory Distress Syndrome, Newborn - diagnostic imaging</subject><subject>Respiratory Distress Syndrome, Newborn - drug therapy</subject><subject>Vascular Surgery</subject><issn>0172-0643</issn><issn>1432-1971</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp9kc1q3TAQhUVpaW7TPkA3RdC105Fl2VZ3rtumgUADSddClsb3KthykOTCfZk-axXcHwIhzEIwOt8ZOIeQtwzOGEDzIQKUVV0AyELWZVvUz8iOVbwsmGzYc7ID1pQF1BU_Ia9ivAWAFlrxkpyUADVnQu7IrwtvlxnTQRvn6dVBh1mbxR69np2JtAtIuylhQEuHI71ew6hN0j59pB29WmJ0w4S0P-hpQr9HmhbaryGgT_SB8eclOr-n56uzODmPkfYBdcqun3Bc8pH_zrT7qd2kBze5dHxNXox6ivjmz3tKfnz9ctN_Ky6_n1_03WVhKsFTMYIEYwRyy-pKSNG0DRs558JYlEPLW2srXnEtaznaljey4rUQJWjeDFoKzU_J-813rydUzo9LCtrMLhrVNUwI1nAos-rsEVUeizmtxePo8v4BwDbAhJxVwFHdBTfrcFQM1H2FaqtQ5QrVfYWqzsy7jblbhxntP-JvZ1lQboKYv3LoQd0ua_A5nidcfwOjcqdb</recordid><startdate>20100501</startdate><enddate>20100501</enddate><creator>McPherson, Christopher</creator><creator>Gal, Peter</creator><creator>Ransom, J. Laurence</creator><creator>Carlos, Rita Q.</creator><creator>Dimaguila, Mary Ann V. T.</creator><creator>Smith, McCrae</creator><creator>Davonzo, Christie</creator><creator>Wimmer, John E.</creator><general>Springer-Verlag</general><general>Springer</general><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>20100501</creationdate><title>Indomethacin Pharmacodynamics Are Altered by Surfactant: A Possible Challenge to Current Indomethacin Dosing Guidelines Created Before Surfactant Availability</title><author>McPherson, Christopher ; Gal, Peter ; Ransom, J. Laurence ; Carlos, Rita Q. ; Dimaguila, Mary Ann V. 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Laurence</creatorcontrib><creatorcontrib>Carlos, Rita Q.</creatorcontrib><creatorcontrib>Dimaguila, Mary Ann V. T.</creatorcontrib><creatorcontrib>Smith, McCrae</creatorcontrib><creatorcontrib>Davonzo, Christie</creatorcontrib><creatorcontrib>Wimmer, John E.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Pediatric cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McPherson, Christopher</au><au>Gal, Peter</au><au>Ransom, J. Laurence</au><au>Carlos, Rita Q.</au><au>Dimaguila, Mary Ann V. T.</au><au>Smith, McCrae</au><au>Davonzo, Christie</au><au>Wimmer, John E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Indomethacin Pharmacodynamics Are Altered by Surfactant: A Possible Challenge to Current Indomethacin Dosing Guidelines Created Before Surfactant Availability</atitle><jtitle>Pediatric cardiology</jtitle><stitle>Pediatr Cardiol</stitle><addtitle>Pediatr Cardiol</addtitle><date>2010-05-01</date><risdate>2010</risdate><volume>31</volume><issue>4</issue><spage>505</spage><epage>510</epage><pages>505-510</pages><issn>0172-0643</issn><eissn>1432-1971</eissn><abstract>The effect of surfactant administration for respiratory distress syndrome (RDS) on indomethacin (INDO) pharmacodynamics and dosing requirements for patent ductus arteriosus (PDA) closure and renal toxicity was evaluated. A 22-year prospective cohort study including 442 INDO-treated patients given 466 INDO treatment courses. The database included demographic information, medical problems, and medications. Neonates with a PDA confirmed by echocardiography were treated with INDO, 0.25–0.3 mg/kg. Subsequent INDO dosing was based on a combined pharmacokinetic/pharmacodynamic (PK/PD) approach. Data were fit to an Emax model and ANOVA was used to compare mean closure levels between groups. PDA closure was successful in 405 of 442 patients (91.6%) and in 434 of 466 treatment courses (93.1%) using an individualized PK/PD dosing approach. Renal toxicity was documented in 56 of 442 patients (12.7%) or 56 of 466 treatment courses (12.0%). Patients not treated with synthetic surfactant trended toward lower mean INDO concentrations at PDA closure compared to patients treated with synthetic surfactant (1.65 vs. 2.01 mg/l;
P
> 0.05) and significantly lower mean INDO concentrations at PDA closure compared to patients treated with natural surfactant (1.65 vs. 2.15 mg/l;
P
< 0.002). This requires an increased total dose of ~0.3 mg/kg or an individual dose increase of 0.1 mg/kg. Administration of natural or synthetic surfactant for RDS may increase the INDO concentrations and doses needed for PDA closure in premature infants.</abstract><cop>New York</cop><pub>Springer-Verlag</pub><pmid>20063159</pmid><doi>10.1007/s00246-009-9628-6</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Animals Anti-Inflammatory Agents, Non-Steroidal - administration & dosage Anti-Inflammatory Agents, Non-Steroidal - pharmacokinetics Anti-Inflammatory Agents, Non-Steroidal - toxicity Biological Availability Biological Products - administration & dosage Calfactant Cardiac Surgery Cardiology Care and treatment Cohort Studies Congenital heart disease Dose-Response Relationship, Drug Drug Administration Schedule Drug Combinations Drug Interactions Ductus Arteriosus, Patent - blood Ductus Arteriosus, Patent - diagnostic imaging Ductus Arteriosus, Patent - drug therapy Echocardiography Echocardiography, Doppler, Color Fatty Alcohols - administration & dosage Guideline Adherence Humans Indomethacin Indomethacin - administration & dosage Indomethacin - pharmacokinetics Indomethacin - toxicity Infant, Newborn Intensive Care Units, Neonatal Kidney - drug effects Medical research Medicine Medicine & Public Health Medicine, Experimental Metabolic Clearance Rate Neonatology Original Article Phosphorylcholine - administration & dosage Polyethylene Glycols - administration & dosage Prospective Studies Pulmonary Surfactants - administration & dosage Respiratory Distress Syndrome, Newborn - blood Respiratory Distress Syndrome, Newborn - diagnostic imaging Respiratory Distress Syndrome, Newborn - drug therapy Vascular Surgery |
title | Indomethacin Pharmacodynamics Are Altered by Surfactant: A Possible Challenge to Current Indomethacin Dosing Guidelines Created Before Surfactant Availability |
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