Literature DB >> 9195117

Cyclosporin pharmacokinetics in paediatric transplant recipients.

G F Cooney1, K Habucky, K Hoppu.   

Abstract

Cyclosporin is an essential component of the antirejection drug protocol used in the long term management of paediatric organ transplant recipients. This article looks at the pharmacokinetics of cyclosporin in paediatric kidney, heart, liver and bone marrow transplant recipients and critically evaluates its relationship to pharmacokinetic data in adult transplant recipients. There are limited data on the pharmacokinetics of cyclosporin in paediatric transplant recipients (14 publications provide the database) as compared with the adult transplant population. Study design, analytical methodology and age ranges of the individuals differ between studies, making comparative interpretation of pharmacokinetic data difficult. However, significant trends are noteworthy and these may influence dose administration guidelines and therapeutic monitoring standards for cyclosporin in the paediatric organ transplant recipient. The bioavailability of the oral formulations of cyclosporin is highly variable as with the adult population, but there appears to be a correlation between cyclosporin bioavailability and age with both the traditional oral formulation (Sandimmun) and the new microemulsion formulation (Neoral) in young liver transplant patients. Bowel length, presystemic metabolism in the gut wall, type of transplant and time since transplant are contributing factors in the variation of bioavailability patterns in paediatric transplant patients. The volume of distribution of cyclosporin does not appear to differ between paediatric and adult transplant recipients, but systemic clearance is comparatively higher in the paediatric population. In general, paediatric patients require higher doses of cyclosporin to achieve target blood concentrations of the drug which are equivalent to the values used in the adult population. Younger patients (less than 8 years of age) may be managed more effectively with a 3 times daily administration schedule rather than the twice daily schedule which is universally used for cyclosporin in the transplant population. The comparatively higher doses and more frequent administration schedule used in paediatric transplant recipients are the consequence of age-related differences in bioavailability and the possibility of increased metabolic clearance of the drug in younger patients.

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Year:  1997        PMID: 9195117     DOI: 10.2165/00003088-199732060-00004

Source DB:  PubMed          Journal:  Clin Pharmacokinet        ISSN: 0312-5963            Impact factor:   6.447


  67 in total

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Authors:  G Appel
Journal:  Kidney Int       Date:  1991-01       Impact factor: 10.612

2.  Comparison of conventional oral cyclosporine and cyclosporine microemulsion formulations in children with a liver transplant.

Authors:  K Hoppu; H Jalanko; J Laine; C Holmberg
Journal:  Transplantation       Date:  1996-07-15       Impact factor: 4.939

3.  Effect of bile on cyclosporin absorption in liver transplant patients.

Authors:  M U Mehta; R Venkataramanan; G J Burckart; R J Ptachcinski; B Delamos; S Stachak; D H Van Thiel; S Iwatsuki; T E Starzl
Journal:  Br J Clin Pharmacol       Date:  1988-05       Impact factor: 4.335

4.  Relationship between corticosteroid exposure and plasma lipid levels in heart transplant recipients.

Authors:  D M Becker; B Chamberlain; R Swank; M G Hegewald; R Girardet; K L Baughman; P O Kwiterovich; T A Pearson; W H Ettinger; D Renlund
Journal:  Am J Med       Date:  1988-11       Impact factor: 4.965

5.  Causes of death after liver transplantation in children treated with cyclosporine and steroids.

Authors:  Delawir Khan; Carlos O Esquivel; Leonard Makowka; Manuel Madrigal-Torres; Eduardo Yunis; Shunzahure Iwatsukl; Thomas E Starzl
Journal:  Clin Transplant       Date:  1989       Impact factor: 2.863

6.  Cyclosporine kinetics in renal transplantation.

Authors:  R J Ptachcinski; R Venkataramanan; J T Rosenthal; G J Burckart; R J Taylor; T R Hakala
Journal:  Clin Pharmacol Ther       Date:  1985-09       Impact factor: 6.875

Review 7.  Pathophysiological and disease-induced changes in drug distribution volume: pharmacokinetic implications.

Authors:  U Klotz
Journal:  Clin Pharmacokinet       Date:  1976       Impact factor: 6.447

8.  Cyclosporin metabolism by human gastrointestinal mucosal microsomes.

Authors:  I R Webber; W H Peters; D J Back
Journal:  Br J Clin Pharmacol       Date:  1992-06       Impact factor: 4.335

9.  Cyclosporine pharmacokinetics in nephrotic and kidney-transplanted children.

Authors:  E Jacqz-Aigrain; C Montes; P Brun; C Loirat
Journal:  Eur J Clin Pharmacol       Date:  1994       Impact factor: 2.953

10.  Cyclosporine dosing and its relationship to outcome in pediatric renal transplantation.

Authors:  W E Harmon; E K Sullivan
Journal:  Kidney Int Suppl       Date:  1993-10       Impact factor: 10.545

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  25 in total

1.  Steroid-sparing effect of tacrolimus in a patient with juvenile dermatomyositis presenting poor bioavailability of cyclosporine A.

Authors:  Akiko Yamada; Yusei Ohshima; Nemuko Omata; Motoko Yasutomi; Mitsufumi Mayumi
Journal:  Eur J Pediatr       Date:  2004-07-08       Impact factor: 3.183

2.  Reduced Exposure to Piperaquine, Compared to Adults, in Young Children Receiving Dihydroartemisinin-Piperaquine as Malaria Chemoprevention.

Authors:  Meghan E Whalen; Richard Kajubi; Nona Chamankhah; Liusheng Huang; Francis Orukan; Erika Wallender; Moses R Kamya; Grant Dorsey; Prasanna Jagannathan; Philip J Rosenthal; Norah Mwebaza; Francesca T Aweeka
Journal:  Clin Pharmacol Ther       Date:  2019-07-22       Impact factor: 6.875

Review 3.  Cytochrome P450 3A: ontogeny and drug disposition.

Authors:  S N de Wildt; G L Kearns; J S Leeder; J N van den Anker
Journal:  Clin Pharmacokinet       Date:  1999-12       Impact factor: 6.447

Review 4.  Immunosuppressive therapy for paediatric transplant patients: pharmacokinetic considerations.

Authors:  María del Mar Fernández De Gatta; Dolores Santos-Buelga; Alfonso Domínguez-Gil; María José García
Journal:  Clin Pharmacokinet       Date:  2002       Impact factor: 6.447

Review 5.  Guidelines on paediatric dosing on the basis of developmental physiology and pharmacokinetic considerations.

Authors:  Imke H Bartelink; Carin M A Rademaker; Alfred F A M Schobben; John N van den Anker
Journal:  Clin Pharmacokinet       Date:  2006       Impact factor: 6.447

6.  Age effect on whole blood cyclosporine concentrations following oral administration in children with nephrotic syndrome.

Authors:  Katsumi Ushijima; Osamu Uemura; Takuji Yamada
Journal:  Eur J Pediatr       Date:  2011-11-26       Impact factor: 3.183

7.  Cyclosporine A monitoring--how to account for twice and three times daily dosing.

Authors:  Samuel Fanta; Janne T Backman; Paula Seikku; Christer Holmberg; Kalle Hoppu
Journal:  Pediatr Nephrol       Date:  2005-03-17       Impact factor: 3.714

Review 8.  Distribution of cyclosporin in organ transplant recipients.

Authors:  Fatemeh Akhlaghi; Andrew K Trull
Journal:  Clin Pharmacokinet       Date:  2002       Impact factor: 6.447

9.  Two-hour post-dose cyclosporin A levels in adolescent renal transplant recipients in the late post-transplant period.

Authors:  Salih Kavukçu; Alper Soylu; Mehmet Türkmen; Belde Kasap; Mukaddes Gümüştekin; Hüseyin Gülay
Journal:  Pediatr Nephrol       Date:  2004-03-31       Impact factor: 3.714

10.  Cyclosporine absorption profiles in pediatric kidney and liver transplant patients.

Authors:  J M Kovarik; Peter F Hoyer; Robert Ettenger; Jeffrey Punch; Marianne Soergel
Journal:  Pediatr Nephrol       Date:  2003-10-24       Impact factor: 3.714

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