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Poster number: PKP-008 · IMPROVING THE QUALITY OF CLINICAL DECISION MAKING BASED ON TOTAL...

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IMPROVING THE QUALITY OF CLINICAL DECISION MAKING BASED ON TOTAL PHENYTOIN SERUM LEVELS Poster number: PKP-008 R. Juvany 1 , M. Colls 1 , M. Dastis 2 , L. Santulario 1 , E. Leiva 1 , S. Cobo 1 , D. Dot 2 , R. Jódar 1 . 1 Hospital Universitari de Bellvitge, Pharmacy department, Hospitalet de Llobregat, Spain. 2 Hospital Universitari de Bellvitge, Clinical Laboratory, Hospitalet de Llobregat, Spain. To design and implement an algorithm, in accordance with the Clinical Laboratory, that includes the albumin serum measurement whenever THPEL is requested in routine testing in hospitalized patients, with the purpose to facilitate the correct interpretation on THPEL. BACKGROUND RESULTS N= 561 THPEL (206 patients; average age: 60.5 years; 119 female). PURPOSE MATERIALS AND METHODS CONCLUSIONS Therapeutic drug monitoring of phenytoin in basis of total phenytoin level (TPHEL) can be misleading in patients with serum albumin < 44 g/L, needing correction before use in clinical decision-making. However, serum albumin isn't always requested with phenytoin measurement. The majority of hospitalized patients had albumin inferior to 44 g/L, requiring the calculation of AATPHEL to optimize clinical decisions. The collaboration between the Clinical Laboratory and the Pharmacy Service has facilitated the availability of serum albumin values for nearly 90% of TPHEL thus improving quality in TPHEL interpretation. Retrospective observational study of hospitalized patients between January 2013 - August 2014. - Variables collected: age, sex, TPHEL, albumin, creatinine and urea serum values. - Phenytoin therapeutic interval: 10-20 mg/L. - Albumin-adjusted total phenytoin level (AATPHEL) by the Sheiner-Tozer equation and GFR by CKD-EPI were calculated Serum albumin analysis in routine testing was determined if it wasn't requested on the same day as phenytoin measurement. TPHEL and AATPHEL results was classified into infra, supra or therapeutic groups and discrepancies among groups were analyzed. 74 (13%) TPHEL did not have albumin results because were stat requests. 98.8% of TPHEL (481 out of 487) had serum albumin < 44 g/L and required correction and 93% of them (449 out of 481) had GFR > 25 mL/min/1.73 m2. 13% 92% 7% 1% 87% No albumin serum values Albumin<44g/L & GFR>25mL/min/1,73m2 Albumin<44g/L & GFR<25mL/min/1,73m2 Albumin>44g/L 0 5 10 15 20 25 30 35 40 45 50 55 Dose increment Dose reduction No dose modification 44 16 40 27 38 35 THPEL AATHPEL Percentage (%) Based on the TPHEL alone, 44% required an increased dose while only 27% required it when using AATPHEL. In contrast, 16% of TPHEL results required dose reduction, which jumped to 38% when AATPHEL was used.
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Page 1: Poster number: PKP-008 · IMPROVING THE QUALITY OF CLINICAL DECISION MAKING BASED ON TOTAL PHENYTOIN SERUM LEVELS Poster number: PKP-008 R. Juvany 1, M. Colls 1, M. Dastis

IMPROVING THE QUALITY OF CLINICAL DECISION MAKING

BASED ON TOTAL PHENYTOIN SERUM LEVELS

Poster number: PKP-008 R. Juvany

1, M. Colls

1, M. Dastis

2, L. Santulario

1, E. Leiva

1, S. Cobo

1, D. Dot

2, R. Jódar

1.

1Hospital Universitari de Bellvitge, Pharmacy department, Hospitalet de Llobregat, Spain.

2Hospital Universitari de Bellvitge, Clinical Laboratory, Hospitalet de Llobregat, Spain.

To design and implement an algorithm, in accordance

with the Clinical Laboratory, that includes the albumin

serum measurement whenever THPEL is requested in

routine testing in hospitalized patients, with the

purpose to facilitate the correct interpretation on

THPEL.

BACKGROUND

RESULTS

N= 561 THPEL (206 patients; average age: 60.5 years; 119 female).

PURPOSE

MATERIALS AND METHODS

CONCLUSIONS

Therapeutic drug monitoring of phenytoin in basis of

total phenytoin level (TPHEL) can be misleading in

patients with serum albumin < 44 g/L, needing

correction before use in clinical decision-making.

However, serum albumin isn't always requested with

phenytoin measurement.

The majority of hospitalized patients had albumin inferior to 44 g/L, requiring the calculation of AATPHEL to

optimize clinical decisions.

The collaboration between the Clinical Laboratory and the Pharmacy Service has facilitated the availability of

serum albumin values for nearly 90% of TPHEL thus improving quality in TPHEL interpretation.

Retrospective observational study of hospitalized patients between January 2013 - August 2014.

- Variables collected: age, sex, TPHEL, albumin, creatinine and urea serum values.

- Phenytoin therapeutic interval: 10-20 mg/L.

- Albumin-adjusted total phenytoin level (AATPHEL) by the Sheiner-Tozer equation and GFR by CKD-EPI were

calculated

Serum albumin analysis in routine testing was determined if it wasn't requested on the same day as phenytoin

measurement.

TPHEL and AATPHEL results was classified into infra, supra or therapeutic groups and discrepancies among

groups were analyzed.

74 (13%) TPHEL did not have albumin results because

were stat requests.

98.8% of TPHEL (481 out of 487) had serum albumin

< 44 g/L and required correction and 93% of them (449

out of 481) had GFR > 25 mL/min/1.73 m2.

13%

92%

7%

1%

87%

No albumin serum values

Albumin<44g/L & GFR>25mL/min/1,73m2

Albumin<44g/L & GFR<25mL/min/1,73m2

Albumin>44g/L

0

5

10

15

20

25

30

35

40

45

50

55

Doseincrement

Dosereduction

No dosemodification

44

16

40

27

38

35

THPEL

AATHPEL

Percentage (%)

Based on the TPHEL alone, 44% required an

increased dose while only 27% required it when using

AATPHEL.

In contrast, 16% of TPHEL results required dose

reduction, which jumped to 38% when AATPHEL was

used.

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