Table 1.
Time points/medical treatment | Creatinine mg/dl (RI 0.8–1.6) |
Urea mg/dl (RI 30–60) |
UPC (<0.2) |
USG | TP g/dl (RI 6–8.2) |
Alb g/dl (RI 2.5–3.9) |
---|---|---|---|---|---|---|
Diagnosis – Started on allopurinol 10 mg/kg PO q12h – Allopurinol stopped 5 days later owing to a suspicion of CADR |
0.9 | 62.5 | 0.6 | 1.035 | 9 | 1.5 |
Day 0 – Started on meglumine antimoniate 50 mg/kg SC q24h |
1.2 | 75.9 | 0.6 | 1.035 | 9.6 | 2.5 |
Day 10 – Meglumine antimoniate was continued |
1.2 | 20 | * | 1.025 | 9.6 | 2.7 |
Day 25 – Meglumine antimoniate was discontinued – Hospitalisation for fluid therapy, supportive and ocular treatment |
6.5 | 119 | * | 1.030 | 9.1 | 2.8 |
Day 34 – Hospital discharge |
0.9 | 31.4 | * | * | * | * |
Day 44 – Started on N-AHCC ½ tablet PO q24h + benazepril 0.5 mg/kg PO q24h |
1.8 | 117.8 | 0.4 | 1.030 | 7.58 | 3.59 |
Day 123 – N-AHCC + benazepril were continued |
1.89 | 93.4 | 0.3 | 1.030 | 8.8 | 3.0 |
Day 162 – Started on miltefosine 2 mg/kg PO q24h for 28 days; N-AHCC + benazepril were continued |
1.9 | 83 | 0.3 | 1.028 | 8.8 | 2.9 |
Day 180 – Hospitalisation for fluid therapy and supportive treatment. Miltefosine and N-AHCC were continued; benazepril was discontinued |
3.84 | 141.9 | * | * | 9.35 | 2.96 |
Day 188 – Hospital discharge |
1.96 | 103.8 | <0.2 | * | * | * |
Day 204 – N-AHCC, renal diet, SC regular fluid therapy, intermittent administration of maropitant |
2.33 | 120.6 | <0.2 | 1.028 | * | * |
Day 213 – Same medical therapy and diet |
3.28 | 198.9 | * | 1.025 | 8.19 | 3.1 |
Day 268 – Same medical therapy and diet |
3.67 | 138.1 | * | 1.028 | 8.57 | 3.16 |
Day 315 – Same medical therapy and diet |
3.31 | 115 | <0.2 | 1.025 | 8.2 | 3.14 |
RI = reference interval; CADR = cutaneous adverse drug reaction; N-AHCC = nucleotides and active hexose correlated compounds
refers to missing data at each time-point