Pharmacokinetics and Safety of Metronidazole in Preterm Infants: Validation of Dried Blood Spot Sampling Mario Sampson, PharmD Duke Clinical Research Institute.

Slides:



Advertisements
Similar presentations
The Execution and Management of a Complex Clinical Trial Elizabeth K. Walsh, RN ECTSS 2013 Conflicts of Interest Advisory Board for TAVR Administrators.
Advertisements

Azithromycin Pharmacokinetics in Pregnancy James H. Fischer, Pharm.D., FCCP May 17, 2011.
Great Ormond Street Hospital for Children NHS Trust The School of Pharmacy UCL INSTITUTE OF CHILD HEALTH Centre for Paediatric Pharmacy Research Drug Development.
PEDIATRIC TRIALS NETWORK March 27, 2014 A project of the Best Pharmaceuticals for Children Act.
1 Effect of Maternal HAART on Postnatal HIV-1 Transmission after Cessation of Extended Infant Antiretroviral Prophylaxis Taha Taha 1, Johnstone Kumwenda.
Poster will be available at after September 10 th 2006 ABSTRACT AN2690 is a new novel antifungal being developed for the treatment of onychomycosis.
Copyright restrictions may apply JAMA Pediatrics Journal Club Slides: Glove Use to Prevent Infections in Preterm Infants Kaufman DA, Blackman A, Conaway.
Copyright restrictions may apply JAMA Pediatrics Journal Club Slides: Surgery and Neurodevelopmental Outcome of VLBW Infants Morriss FH Jr, Saha S, Bell.
Q II Case Study: Surfactant Use in Preterm Infants Laura C. Leviton, PhD Gautham Suresh, MD for the TRIP Investigators.
Once-Daily Regimen of FTC, DDI, EFV in ARV Therapy- Naïve Children PACTG 1021.
“Association of OPRM1 and COMT Single Nucleotide Polymorphisms with Hospital Length of Hospital Stay and Treatment of Neonatal Abstinence Syndrome” E Wachman,
What’s different about paediatric prescribing.  Vary in their developmental stages ◦ Pre-term, neonates, infants, children, adolescents  Dynamic anatomy.
The higher BUP-to-NBUP ratio (0.7—19.19) than adults (0.165—1.4) has been observed in newborn patients studied. It might be due to immature hepatic function.
The impact of managed clinical networks on place of birth and newborn transfers Chris Gale On behalf of the Neonatal Data Analysis Unit and the Medicines.
Updates and Lessons Learned from Pediatric Trials Network (PTN) Michael Cohen-Wolkowiez, MD, PhD Assistant Professor Duke University Michael Cohen-Wolkowiez,
1 One Year Post-Exclusivity Adverse Event Review: Ertapenem Pediatric Advisory Committee Meeting November 16, 2006 Alan M. Shapiro, MD, PhD, FAAP Medical.
Clinical Pharmacology Subcommittee of the Advisory Committee for Pharmaceutical Science Meeting April 22, 2003 Pediatric Population Pharmacokinetics Study.
Programs for HIV Prevention and TreatmentIRD UMI 174 Pediatric HIV Clinical Pharmacology Program Development in Thailand Tim R. Cressey Research Associate,
Gastroschisis and Mode of Delivery: National Trends and Evaluation of Outcomes, 1991 to 2005 T. Mac Bird University of Arkansas for Medical Sciences College.
Copyright © 2013, 2010 by Saunders, an imprint of Elsevier Inc. Chapter 10 Drug Therapy in Pediatric Patients.
POSTER TEMPLATES BY: Introduction Results Discussion References Study Objective(s) Methods (Continued) Specify the objective(s)
Phase III trial of pafuramidine maleate (DB289), a novel, oral drug, for treatment of first stage sleeping sickness Introduction Only a very limited number.
For Clinical Pharmacist
A Population Based Survey of Infant Inconsolability and Postpartum Depression Pamela C. High*, Rachel Cain**, Hanna Kim** and Samara Viner-Brown** Hasbro.
Pediatric Trials Network. What Is The Pediatric Trials Network PTN? Sponsored by the Eunice Kennedy Shriver National Institute of Child Health and Human.
Newborn Screening Translational Research Network Coordinating Center Duane Alexander, M.D. Director, Eunice Kennedy Shriver National Institute of Child.
Barry T Bloom, MD Presented to The Blue Ribbon Commission on Infant Mortality September 24, 2010 A Proposal Kansas Perinatal Quality Improvement Collaborative.
HIVNET 023 Sponsored by the US National Institute of Allergy and Infectious Diseases, National Institute of Health through the HIV Prevention Trials Network.
Evidence Based Medication Use in the NICU: Erythropoietin Dan Ellsbury MD Director, Continuous Quality Improvement Pediatrix Medical Group.
The impact of academic medical centers on infant mortality rates in five North Carolina counties Timberly Butler, MSII Mentor: Kristen G. Hairston, MD,
FDA Case Studies Pediatric Oncology Subcommittee March 4, 2003.
Population PK-PD Modeling of Anti-Infective Agents
POPULATION PHARMACOKINETICS OF ANTIRETROVIRAL DRUGS IN HCV/HIV OR HBV/HIV CO-INFECTED INDIVIDUALS J.P. Cruz 1,2, D. Matias 1, C. Carvalho 1, J. Morais.
Population Pharmacokinetic Characteristics of Levosulpiride and Terbinafine in Healthy Male Korean Volunteers Yong-Bok Lee College of Pharmacy and Institute.
APPLICATION OF INDIVIDUALIZED BAYESIAN UREA KINETIC MODELING TO PEDIATRIC HEMODIALYSIS Olivera Marsenic, Athena Zuppa, Jeffrey S. Barrett, Marc Pfister.
DISEASES OF ALVEOLAR HOMEOSTASIS: RDS and BPD
FDA/CBER Vaccines and Related biological Products Advisory Committee Meeting Discussion of Clinical Trials to Support use of Vaccines against the 2009.
The effect of fluvoxamine on the pharmacokinetics, and safety of ivabradine in healthy subjects Adina Popa 1, Laurian Vlase 2, Maria Neag 3, Dana Muntean.
Rivaroxaban Has Predictable Pharmacokinetics (PK) and Pharmacodynamics (PD) When Given Once or Twice Daily for the Treatment of Acute, Proximal Deep Vein.
Evaluation of Current Vancomycin Dosing Practices and Pharmacokinetic Neonatal Infant Models with Therapeutic Drug Monitoring Data from a Pediatric Population.
Noncompartmental Models. Introduction The noncompartmental approach for data analysis does not require any specific compartmental model for the system.
BACKGROUND OBJECTIVES DESIGN / METHODS DISCUSSION AND CONCLUSIONS The PPK model is well predicted; pediatric anti-Xa exposure of dalteparin is well characterized.
Summer Research Training Program an opportunity to participate – in virtually all aspects of a research project with the guidance of a faculty research.
Background Derma-Smoothe/FS ® (Fluocinolone acetonide ) Contains 0.01% fluocinolone acetonide in an oil base solution, Categorized as a low to medium potency.
Validation and Refinement of a Prediction Rule to Identify Children at Low Risk for Acute Appendicitis Kharbanda AB, Dudley NC, Bajaj L, et al; Pediatric.
1 EFFICACY OF SHORT COURSE AMOXICILLIN FOR NON-SEVERE PNEUMONIA IN CHILDREN (Hazir T*, Latif E*, Qazi S** AND MASCOT Study Group) *Children’s Hospital,
Iman Al-Obari, Ms Pharm; Abdulrazaq Al-Jazairi, PharmD; Iman Zaghloul, PhD; Mahasen Saleh, MD Ali Sanei, MD; Aabdulrahman Al Mousa, MD; Zuhair Al-Halees,
Systemic Exposure of Topical Tacrolimus Veneeta Tandon, Ph.D. Pharmacokinetics Reviewer Division of Pharmaceutical Evaluation III Office of Clinical Pharmacology.
Integrated Mother-Premature Infant Intervention and Mother-Infant Interaction at 6-weeks Corrected Age Rosemary White-Traut, PhD, RN, FAAN Kathleen Norr,
Pharmacokinetics of Vancomycin in Adult Oncology Patients Hadeel Al-Kofide MS.c; Iman Zaghloul PhD; and Lamya Al-Naim PharmD Department of Clinical Pharmacy,
C-1 Pegfilgrastim (Neulasta  ) Oncologic Drugs Advisory Committee Pediatric Subcommittee October 20, 2005 Amgen Inc.
INTERMITTENT IV VANCOMYCIN WHAT DOSE SHOULD WE START WITH?
Copyright ©2008 by Pearson Education, Inc. Upper Saddle River, New Jersey All rights reserved. Focus on Pharmacology, First Edition By Jahangir Moini.
Effect of Captopril first doses on Blood Pressure and Renal Function in Children with Congestive Cardiac Failure Dr Hussain Mulla, Co-Director, Centre.
1 Pharmacokinetic Information Submitted to Support Valganciclovir Use in Maintenance Therapy for CMV Retinitis Robert O. Kumi, Ph.D. Reviewer, Pharmacokinetics.
Meeting the ACGME Milestones through Group Prenatal Care INTRODUCTION Mila D'Cunha MD. MSc., Anastasia Kolasa-Lenarz MD. MPH., Karolina Lis MD., Kimberly.
A Survival Comparison between HIV+ U.S.-born Latinos and Foreign-born Latinos in Houston, Texas Raouf Arafat, MD, MPH, Adebowale Awosika- Olumo.
Effect of Four Different Meal Types on the Population Pharmacokinetics of Single Dose of Rifapentine in Healthy Male Volunteers Simbarashe P. Zvada 1,
Society for Prevention Research 21st Annual Meeting (May 28-31, 2013) in San Francisco, CA A. Fogarasi-Grenczer 1, I. Rákóczi 2, K. L. Foley PhD. 3, P.
Overall support for the International Maternal Pediatric Adolescent AIDS Clinical Trials (IMPAACT) Network was provided by the National Institute of.
A Healthier Tomorrow Begins Today National Immunization Conference 2004.
Drug Therapy in Pediatric Patients
Gregory L. Kearns, PharmD, FCP 
17-alpha Hydroxyprogesterone caproate did not reduce the rate of recurrent preterm birth in a prospective cohort study David B. Nelson, MD; Donald D. McIntire,
Bioanalysis validation: case example
Morphine pharmacokinetics and pharmacodynamics in preterm and term neonates: secondary results from the NEOPAIN trial  K.J.S. Anand, B.J. Anderson, N.H.G.
Advances in Microsampling and Considerations for Interpretation of Results Kenneth Lewis, Ph.D. OpAns, LLC RTP, NC.
Yang Liu, Anne Chain, Rebecca Wrishko,
Drug Therapy in Pediatric Patients
Number of infants in different populations with birth weight < 1500 g who received exchange transfusions between 1974 and Number of infants in different.
Presentation transcript:

Pharmacokinetics and Safety of Metronidazole in Preterm Infants: Validation of Dried Blood Spot Sampling Mario Sampson, PharmD Duke Clinical Research Institute University of North Carolina Eshelman School of Pharmacy

Background n In preterm infants, intra-abdominal infections are deadly n These infections are polymicrobial, including anaerobes n Metronidazole has excellent anti-anaerobic activity n Pharmacokinetic data of metronidazole in preterm infants are limited n Blood volume is a limiting factor for studies in neonates l Dried blood spots require 10 times less blood per sample vs. plasma

Methods n Multicenter (N=3), open-label, PK study n N=24 n Population l Gestational age at birth <32 weeks l Postnatal age (PNA) <91 days l Suspected serious infection n Dosing (intravenous) l Loading dose 15 mg/kg l Maintenance dose 7.5 mg/kg every hours for 5 days

Methods Last dose, PNA < 14 days hours hours Last dose, PNA ≥ 14 days Dose 1, & hours n Sampling l Paired plasma and dried blood spots collected if possible n Population PK l Nonlinear mixed effects modeling using NONMEM software and bootstrapping to evaluate precision of parameters l Plasma and dried blood spot samples analyzed separately n Plasma and dried blood spot paired concentrations analyzed by linear regression

Subject Demographics

Population Pharmacokinetics n Final model: Clearance (L/h) = * Weight * (Postnatal Age/27) and Volume (L) = * Weight

Population Pharmacokinetic Parameters

Dried Blood Spots r 2 =0.85, p<0.001 N=46 paired samples r 2 =0.95, slope=0.80 [95% CI, 0.74, 0.85], p<0.001

Adverse Events

Conclusions n Metronidazole clearance increased with postnatal age l Clearance finding expected with development n The bias in population clearance and volume parameter estimates was <10% using dried blood spots n DBS sampling can be used to evaluate metronidazole pharmacokinetics n Pediatric Trials Network l Daniel Benjamin Jr. l Edmund Capparelli l Gregory Kearns l Philip Brian Smith l Michael Cohen-Wolkowiez l Katherine Berezny l Barrie Harper n Enrolling Sites l Children’s Hospital of Orange County - Antonio Arrieta l Duke University Medical Center - James Wynn l Wesley Medical Center - Barry Bloom - Paula Delmore n Data Coordinating Center l EMMES Corporation n NIGMS/NICHD UNC-Duke Collaborative T32 Clinical Pharmacology Postdoctoral Training Grant, National Institutes of Health (1 T32 GM 86330) l Kim Brouwer l Daniel Benjamin Jr. l Paul Watkins n Eunice Kennedy Shriver National Institute of Child Health and Human Development (NIH) l Contract #: HHSN and HHSN I l Task Order #: HHSN n Best Pharmaceuticals for Children Act n University of North Carolina Eshelman School of Pharmacy Acknowledgments