Optimizing lithium dosing in hemodialysis

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Standard

Optimizing lithium dosing in hemodialysis. / Bjarnason, N H; Munkner, R; Kampmann, J P; Tornoe, C W; Ladefoged, Susanne; Dalhoff, K.

I: Therapeutic Drug Monitoring, Bind 28, Nr. 2, 01.04.2006, s. 262-6.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskning

Harvard

Bjarnason, NH, Munkner, R, Kampmann, JP, Tornoe, CW, Ladefoged, S & Dalhoff, K 2006, 'Optimizing lithium dosing in hemodialysis', Therapeutic Drug Monitoring, bind 28, nr. 2, s. 262-6. https://doi.org/10.1097/01.ftd.0000183386.35018.86

APA

Bjarnason, N. H., Munkner, R., Kampmann, J. P., Tornoe, C. W., Ladefoged, S., & Dalhoff, K. (2006). Optimizing lithium dosing in hemodialysis. Therapeutic Drug Monitoring, 28(2), 262-6. https://doi.org/10.1097/01.ftd.0000183386.35018.86

Vancouver

Bjarnason NH, Munkner R, Kampmann JP, Tornoe CW, Ladefoged S, Dalhoff K. Optimizing lithium dosing in hemodialysis. Therapeutic Drug Monitoring. 2006 apr. 1;28(2):262-6. https://doi.org/10.1097/01.ftd.0000183386.35018.86

Author

Bjarnason, N H ; Munkner, R ; Kampmann, J P ; Tornoe, C W ; Ladefoged, Susanne ; Dalhoff, K. / Optimizing lithium dosing in hemodialysis. I: Therapeutic Drug Monitoring. 2006 ; Bind 28, Nr. 2. s. 262-6.

Bibtex

@article{a9a9f82754a24078aa6b40954e6cd8d8,
title = "Optimizing lithium dosing in hemodialysis",
abstract = "We studied a 62-year-old female hemodialysis patient during initiation and maintenance of lithium carbonate therapy. Three different methods were applied to estimate the regimen: a scenario based on volume of distribution (V(d)), a scenario based on glomerular filtration rate (GFR), and a scenario in which we developed an algorithm based on a 2-compartment distribution without elimination. The GFR estimate led to plasma concentrations 3-4 times lower than those anticipated. In contrast, the estimates based on V(d) and the algorithm derived from pharmacokinetic modeling led to comparable loading dose estimates. Furthermore, the maintenance dose estimated from the central compartment (V1) led to plasma concentrations within the therapeutic range. Thus, a regimen where 12.2 mmol lithium was given after each hemodialysis session resulted in stable between-dialysis plasma lithium concentrations in this patient with no residual kidney function. We did not observe adverse effects related to this regimen, which was monitored from 18 days to 8 months of therapy, and the patient experienced relief from her severe depressive disorder. In conclusion, dialysis patients may be treated with lithium administrated immediately postdialysis. Further observations are necessary to obtain robust long-term safety data and to optimize the monitoring schedule.",
author = "Bjarnason, {N H} and R Munkner and Kampmann, {J P} and Tornoe, {C W} and Susanne Ladefoged and K Dalhoff",
year = "2006",
month = apr,
day = "1",
doi = "http://dx.doi.org/10.1097/01.ftd.0000183386.35018.86",
language = "English",
volume = "28",
pages = "262--6",
journal = "Therapeutic Drug Monitoring",
issn = "0163-4356",
publisher = "Lippincott Williams & Wilkins",
number = "2",

}

RIS

TY - JOUR

T1 - Optimizing lithium dosing in hemodialysis

AU - Bjarnason, N H

AU - Munkner, R

AU - Kampmann, J P

AU - Tornoe, C W

AU - Ladefoged, Susanne

AU - Dalhoff, K

PY - 2006/4/1

Y1 - 2006/4/1

N2 - We studied a 62-year-old female hemodialysis patient during initiation and maintenance of lithium carbonate therapy. Three different methods were applied to estimate the regimen: a scenario based on volume of distribution (V(d)), a scenario based on glomerular filtration rate (GFR), and a scenario in which we developed an algorithm based on a 2-compartment distribution without elimination. The GFR estimate led to plasma concentrations 3-4 times lower than those anticipated. In contrast, the estimates based on V(d) and the algorithm derived from pharmacokinetic modeling led to comparable loading dose estimates. Furthermore, the maintenance dose estimated from the central compartment (V1) led to plasma concentrations within the therapeutic range. Thus, a regimen where 12.2 mmol lithium was given after each hemodialysis session resulted in stable between-dialysis plasma lithium concentrations in this patient with no residual kidney function. We did not observe adverse effects related to this regimen, which was monitored from 18 days to 8 months of therapy, and the patient experienced relief from her severe depressive disorder. In conclusion, dialysis patients may be treated with lithium administrated immediately postdialysis. Further observations are necessary to obtain robust long-term safety data and to optimize the monitoring schedule.

AB - We studied a 62-year-old female hemodialysis patient during initiation and maintenance of lithium carbonate therapy. Three different methods were applied to estimate the regimen: a scenario based on volume of distribution (V(d)), a scenario based on glomerular filtration rate (GFR), and a scenario in which we developed an algorithm based on a 2-compartment distribution without elimination. The GFR estimate led to plasma concentrations 3-4 times lower than those anticipated. In contrast, the estimates based on V(d) and the algorithm derived from pharmacokinetic modeling led to comparable loading dose estimates. Furthermore, the maintenance dose estimated from the central compartment (V1) led to plasma concentrations within the therapeutic range. Thus, a regimen where 12.2 mmol lithium was given after each hemodialysis session resulted in stable between-dialysis plasma lithium concentrations in this patient with no residual kidney function. We did not observe adverse effects related to this regimen, which was monitored from 18 days to 8 months of therapy, and the patient experienced relief from her severe depressive disorder. In conclusion, dialysis patients may be treated with lithium administrated immediately postdialysis. Further observations are necessary to obtain robust long-term safety data and to optimize the monitoring schedule.

U2 - http://dx.doi.org/10.1097/01.ftd.0000183386.35018.86

DO - http://dx.doi.org/10.1097/01.ftd.0000183386.35018.86

M3 - Journal article

VL - 28

SP - 262

EP - 266

JO - Therapeutic Drug Monitoring

JF - Therapeutic Drug Monitoring

SN - 0163-4356

IS - 2

ER -

ID: 34107751