Case Report

Fatal Lactic Acidosis in a Kidney Transplant Recipient on Combination Antiretroviral Therapy after Initiation of Tacrolimus Therapy

Table 1

Haematology, biochemistry, thrombosis, and virology test results at various time points prior to and following renal transplantation.

VariableReference range (min, max), adultsPretransplant4–6 weeks prior to tacrolimus initiationOne week following tacrolimus initiationTwo weeks following tacrolimus initiation

Haematology
Haemoglobin (g/dL)13.0, 17.011.812.512.512.9
White cell count ( × 1 0 9 ) 4.0, 11.09.08.812.610.9
Platelet count ( × 1 0 9 ) 150, 400268308255229
CD4 Lymphocytes (per μL)300, 1400118895623521

Coagulation
Activated partial thromboplastin time ratio0.85, 1.160.911.081.231.51
International normalized ratio0.90, 1.101.031.041.101.59

Clinical Chemistry
Sodium (mmol/L)135, 145133136134130
Potassium (mmol/L)3.5, 5.04.34.34.65.1
Bicarbonate (mmol/L)22, 3025261915
Urea (mmol/L)1.7, 8.322.07.814.414.1
Creatinine (μmol/L)59, 1041415156206233
Albumin (g/L)40, 5246463732
Alkaline phosphatase (IU/L)35, 12962205236383
Bilirubin (μmol/L)0, 16761044
Alanine transaminase (IU/L)4, 59362065141
Gamma-glutamyl transferase (IU/L)4, 7242613541500
Creatine kinase (IU/L)0, 229Not measuredNot measuredNot measured1468
Lactic acid (mmol/L)0.4, 2.2Not measuredNot measuredNot measured18

Virology
Hepatitis C RNA (IU/mL)< 15Not measuredNot measured<15
HIV-1 RNA (copies/mL)<40<40Not measured<40
CMV DNA (copies/mL)Not applicableNot detectedNot detectedNot detected

Drug levels
Ciclosporin level (μg/L)100, 200Not applicable74Not applicableNot applicable
Tacrolimus level (μg/L)8, 12Not applicableNot applicable2613

Antiviral medications6 weeks prior to transplantation15 weeks following transplant: on ciclosporinNR2 weeks after switching to tacrolimus
Abacavir (mean steady state §Cmin, Cmax; ng/mL)10, 300015511611NR538
Lamivudine (mean steady state Cmin, Cmax; ng/mL) 90, 12007941615NR717
Nevirapine (therapeutic range min, max; ng/mL)3000, 80005227Not measuredNR5488

Estimated from therapeutic doses of  §300 mg abacavir twice daily and 150 mg lamivudine twice daily (values derived from Delphic Laboratories (Liverpool) ltd.).