ArticleBritish journal of clinical pharmacology1992
The pharmacokinetics and pharmacodynamics of recombinant human erythropoietin in haemodialysis patients.
Article in British journal of clinical pharmacology, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.
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Who cites it
21 citing papers in PubMed.
- Pharmacokinetic and pharmacodynamic profiles of extended dosing of epoetin alfa in anemic patients who have chronic kidney disease and are not on dialysis.Clinical journal of the American Society of Nephrology : CJASN · 2008Trial
- Change in erythropoietin pharmacokinetics following hematopoietic transplantation.Clinical pharmacology and therapeutics · 2007Trial
- Development and evaluation of a population pharmacokinetic-pharmacodynamic model of darbepoetin alfa in patients with nonmyeloid malignancies undergoing multicycle chemotherapy.The AAPS journal · 2006Trial
- Recombinant human erythropoietin for the treatment of renal anaemia in children: no justification for bodyweight-adjusted dosage.Clinical pharmacokinetics · 2004Trial
- Review
- Economic Benefits of Switching From Intravenous to Subcutaneous Epoetin Alfa for the Management of Anemia in Hemodialysis Patients.Canadian journal of kidney health and disease · 2020Article
- Effect of renal function and dialysis modality on daprodustat and predominant metabolite exposure.Clinical kidney journal · 2019Article
- A Randomized Controlled Trial: Regenerative Effects, Efficacy and Safety of Erythropoietin in Burn and Scalding Injuries.Frontiers in pharmacology · 2018Article
- The greatly misunderstood erythropoietin resistance index and the case for a new responsiveness measure.Hemodialysis international. International Symposium on Home Hemodialysis · 2016Article
- Association of Erythropoietin Dose and Route of Administration with Clinical Outcomes for Patients on Hemodialysis in the United States.Clinical journal of the American Society of Nephrology : CJASN · 2015Article
- Clinical pharmacokinetics and pharmacodynamics of erythropoiesis-stimulating agents.Clinical pharmacokinetics · 2013Review
- Predictive modeling for improved anemia management in dialysis patients.Current opinion in nephrology and hypertension · 2011Review
- Erythropoietin dosing in children with chronic kidney disease: based on body size or on hemoglobin deficit?Pediatric nephrology (Berlin, Germany) · 2009Article
- Iron and anemia in human biology: a review of mechanisms.Heart failure reviews · 2008Review
- A 'bottom-up' approach for endo-PK/PD analysis.Biopharmaceutics & drug disposition · 2006Article
- Pharmacodynamic analysis of changes in reticulocyte subtype distribution in phlebotomy-induced stress erythropoiesis.Journal of pharmacokinetics and pharmacodynamics · 2005Article
- Predicting the time course of haemoglobin in children treated with erythropoietin for renal anaemia.British journal of clinical pharmacology · 1998Article
- Pharmacokinetic and pharmacological profiles of free and liposomal recombinant human erythropoietin after intravenous and subcutaneous administrations in rats.Pharmaceutical research · 1997Article
- Epoetin alfa. A review of its clinical efficacy in the management of anaemia associated with renal failure and chronic disease and its use in surgical patients.Drugs & aging · 1995Review
- The pharmacokinetics of recombinant human erythropoietin after subcutaneous injection at different sites.European journal of clinical pharmacology · 1994Article
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
1. The pharmacokinetics of and therapeutic response to recombinant human erythropoietin (rcEPO) were studied in 12 patients under chronic haemodialysis on a thrice weekly intravenous rcEPO treatment scheme. The kinetics of rcEPO were also assessed after a subcutaneous injection during the initial period and during maintenance treatment. RcEPO was measured in plasma by radioimmunoassay. 2. After the first i.v. dose plasma erythropoietin concentrations were best described by a monoexponential disposition function with a mean (+/- s.d.) elimination half-life of 5.4 +/- 1.7 h. The volume of distribution was 70 +/- 5.2 ml kg-1 and the clearance was 10.1 +/- 3.5 ml h-1 kg-1 (n = 12). 3. After 3 months of continuous therapy, the plasma half-life of rcEPO decreased by 15% (P < 0.05, mean half-life during steady state: 4.6 +/- 2.8 h), while mean clearance and volume of distribution remained constant. 4. After the first s.c. injection the mean (+/- s.d.) absorption time was 22 +/- 11 h and systemic availability was 44 +/- 7%. 5. Changes in haemoglobin concentrations were described by a linear additive dose-response model, defined by an efficacy constant (Keff) and the mean erythrocyte lifetime (MRTHb). The sample mean (+/- s.d.) Keff was 0.043 +/- 0.017 g dl-1 Hb per 1000 units rcEPO and MRTHb was 10.02 +/- 1.75 weeks. The net effect of rcEPO treatment was described by the area under the unit-dose-response curve (AUEC) with a mean (+/- s.d.) value of 0.45 +/- 0.23 g dl-1 weeks. 6. RcEPO clearance showed a significant positive correlation (r2 = 0.41) with the effectiveness of rcEPO therapy, as measured by the parameters Keff or AUEC.
Indexed as
Identifiers
1493082PMC1381451What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.