Trimethoprim-sulfamethoxazole: Difference between revisions
From IDWiki
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* Resistant Gram-negative infections |
* Resistant Gram-negative infections |
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** [[Cystitis]]: 160 mg (1 |
** [[Cystitis]] or [[pyelonephritis]]: 160 mg/800 mg (1 DS tab) IV/PO q12h |
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** Other infections: 8 to 12 mg/kg/day IV/PO divided q8-12h (max 960 mg total daily dose) |
** Other infections: 8 to 12 mg/kg/day IV/PO divided q8-12h (max 960 mg total daily dose) |
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*[[Nocardia]]: 10 mg/kg TDD |
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*[[Pneumocystis jirovecii]]: 15-20 mg/kg TDD |
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*CNS infections: 15-20 mg/kg TDD |
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=== Oral Dosing === |
=== Oral Dosing === |
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* 10 to 20 mg/kg TMP total daily dose, split TID to QID |
* 10 to 20 mg/kg TMP total daily dose, split TID to QID |
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⚫ | |||
==== TMP 10 mg/kg per day ==== |
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⚫ | |||
⚫ | |||
! Weight (kg) |
! Weight (kg) |
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! Total dose TMP (mg/day) |
! Total dose TMP (mg/day) |
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!Dose (PO) |
!Dose (PO) |
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|- |
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| rowspan="5" |10 mg/kg |
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| 40-49 |
| 40-49 |
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| 480 |
| 480 |
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| 20 mL q6h |
| 20 mL q6h |
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|2 DS tabs q6h |
|2 DS tabs q6h |
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|} |
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==== TMP 15 mg/kg per day ==== |
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{| class="wikitable" |
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! Weight (kg) |
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! Total dose TMP (mg/day) |
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! Dose (IV) |
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⚫ | |||
|- |
|- |
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| rowspan="9" |15 mg/kg |
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|40-44 |
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|640 |
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|10 mL q6h |
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|1 DS tab q6h, or 2 DS tabs q12h |
|1 DS tab q6h, or 2 DS tabs q12h |
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|- |
|- |
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|45-49 |
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|720 |
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|15 mL q8h |
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|3 SS tabs q8h |
|3 SS tabs q8h |
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|- |
|- |
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|50-69 |
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|960 |
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|15 mL q6h |
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|2 DS tabs q8h, or 3 SS tabs q6h |
|2 DS tabs q8h, or 3 SS tabs q6h |
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|- |
|- |
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|70-79 |
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|1200 |
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|25 mL q8h |
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|5 SS tabs q8h |
|5 SS tabs q8h |
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|- |
|- |
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|80-89 |
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|1280 |
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|20 mL q6h |
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|2 DS tabs q6h |
|2 DS tabs q6h |
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|- |
|- |
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|90-99 |
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|1440 |
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|30 mL q8h |
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|3 DS tabs q8h |
|3 DS tabs q8h |
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|- |
|- |
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|100-109 |
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|1600 |
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|25 mL q6h |
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|2/2/3/3 DS tabs q6h, or 5 SS tabs q6h |
|2/2/3/3 DS tabs q6h, or 5 SS tabs q6h |
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|- |
|- |
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|110-119 |
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|1680 |
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|35 mL q8h |
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|7 SS tabs q8h |
|7 SS tabs q8h |
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|- |
|- |
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|120-129 |
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|1920 |
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|30 mL q6h |
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|3 DS tabs q6h |
|3 DS tabs q6h |
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|} |
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==== TMP 20 mg/kg per day ==== |
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{| class="wikitable" |
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! Weight (kg) |
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! Total dose TMP (mg/day) |
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! Dose (IV) |
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!Dose (PO) |
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|- |
|- |
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| rowspan="7" |20 mg/kg |
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|40-54 |
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|960 |
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|15 mL q6h |
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|2 DS tabs q8h, or 3 SS tabs q6h |
|2 DS tabs q8h, or 3 SS tabs q6h |
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|- |
|- |
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|55-69 |
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|1280 |
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|20 mL q6h |
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|2 DS tabs q6h |
|2 DS tabs q6h |
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|- |
|- |
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|70-79 |
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|1440 |
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|30 mL q8h |
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|3 DS tabs q8h |
|3 DS tabs q8h |
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|- |
|- |
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|80-89 |
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|1600 |
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|25 mL q6h |
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|2/2/3/3 DS tabs q6h, or 5 SS tabs q6h |
|2/2/3/3 DS tabs q6h, or 5 SS tabs q6h |
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|- |
|- |
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|90-104 |
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|1920 |
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|30 mL q6h |
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|3 DS tabs q6h |
|3 DS tabs q6h |
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|- |
|- |
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|105-119 |
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|2240 |
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|35 mL q6h |
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|3/3/4/4 DS tabs q6h, or 7 SS tabs q6h |
|3/3/4/4 DS tabs q6h, or 7 SS tabs q6h |
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|- |
|- |
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|120-134 |
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|2560 |
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|40 mL q6h |
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|4 DS tabs q6h |
|4 DS tabs q6h |
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|} |
|} |
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=== Renal Dosing === |
==== Renal Dosing ==== |
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{| class="wikitable" |
{| class="wikitable" |
Latest revision as of 16:37, 27 September 2024
Background
- Sulfonamide antibiotic
Brand Names
- Septra
- Bactrim (US)
- TMP-SMX
Dosing
- Traditionally based on the trimethroprim component
Form | TMP | SMX | Conversion |
---|---|---|---|
Intravenous | 16 mg/ml | 80 mg/ml | 10 mL |
Oral suspension | 8 mg/ml | 40 mg/ml | 20 mL |
Oral SS tab | 80 mg | 400 mg | 2 tabs |
Oral DS tab | 160 mg | 800 mg | 1 tab |
- Resistant Gram-negative infections
- Cystitis or pyelonephritis: 160 mg/800 mg (1 DS tab) IV/PO q12h
- Other infections: 8 to 12 mg/kg/day IV/PO divided q8-12h (max 960 mg total daily dose)
- Nocardia: 10 mg/kg TDD
- Pneumocystis jirovecii: 15-20 mg/kg TDD
- CNS infections: 15-20 mg/kg TDD
Oral Dosing
- Ranges from 1 SS tab BID (160 mg TMP TDD) to 3 DS tabs TID (1440 mg TMP TDD)
Intravenous Dosing
- 10 to 20 mg/kg TMP total daily dose, split TID to QID
Dose (TMP) | Weight (kg) | Total dose TMP (mg/day) | Dose (IV) | Dose (PO) |
---|---|---|---|---|
10 mg/kg | 40-49 | 480 | 10 mL q8h | 1 DS tab q8h |
50-64 | 640 | 10 mL q6h | 1 DS tab q6h, or 2 DS tabs q12h | |
65-74 | 720 | 15 mL q8h | 3 SS tabs q8h | |
75-99 | 960 | 15 mL q6h | 2 DS tabs q8h, or 3 SS tabs q6h | |
100-129 | 1280 | 20 mL q6h | 2 DS tabs q6h | |
15 mg/kg | 40-44 | 640 | 10 mL q6h | 1 DS tab q6h, or 2 DS tabs q12h |
45-49 | 720 | 15 mL q8h | 3 SS tabs q8h | |
50-69 | 960 | 15 mL q6h | 2 DS tabs q8h, or 3 SS tabs q6h | |
70-79 | 1200 | 25 mL q8h | 5 SS tabs q8h | |
80-89 | 1280 | 20 mL q6h | 2 DS tabs q6h | |
90-99 | 1440 | 30 mL q8h | 3 DS tabs q8h | |
100-109 | 1600 | 25 mL q6h | 2/2/3/3 DS tabs q6h, or 5 SS tabs q6h | |
110-119 | 1680 | 35 mL q8h | 7 SS tabs q8h | |
120-129 | 1920 | 30 mL q6h | 3 DS tabs q6h | |
20 mg/kg | 40-54 | 960 | 15 mL q6h | 2 DS tabs q8h, or 3 SS tabs q6h |
55-69 | 1280 | 20 mL q6h | 2 DS tabs q6h | |
70-79 | 1440 | 30 mL q8h | 3 DS tabs q8h | |
80-89 | 1600 | 25 mL q6h | 2/2/3/3 DS tabs q6h, or 5 SS tabs q6h | |
90-104 | 1920 | 30 mL q6h | 3 DS tabs q6h | |
105-119 | 2240 | 35 mL q6h | 3/3/4/4 DS tabs q6h, or 7 SS tabs q6h | |
120-134 | 2560 | 40 mL q6h | 4 DS tabs q6h |
Renal Dosing
CrCl (mL/min) | Bacterial infection (TMP) | PJP (TMP) |
---|---|---|
> 30 | 8-12 mg/kg/day in 2-4 divided doses | 15-20 mg/kg/day in 2-4 divided doses |
10 to 29 | 75% of usual dose | 12-15 mg/kg/day in 2-4 divided doses |
< 10, including PD | Generally not recommended; use 50% of usual dose | Generally not recommended; use 7.5-10 mg/kg/day in 2-4 divided doses |
Hemodialysis | 50% of usual dose, scheduled post-dialysis | 50% of usual dose, scheduled post-dialysis |
CRRT | 7.5 mg/kg/day in 2-4 divided doses | 15 mg/kg/day in 2-4 divided doses |
Adverse Drug Reactions
- Systemic allergic reactions
- Cutaneous reactions
- High rate of SJS/TEN
- Other non-specific rash
- Erythema multiforme
- Urticaria
- Photodermatitis
- GI upset, including nausea at higher doses
- Drug-drug interactions
- Increases warfarin levels
- Anemia, neutropenia and thrombocytopenia
- It is a mild folate antagonist
- Hepatotoxicity
- Hyperkalemia
- Hyponatremia
- Hypoglycemia
- Acute kidney injury, though it also increases tubular creatinine reabsorption
- Renal tubular acidosis
Further Reading
- Considerations when prescribing trimethoprim-sulfamethoxazole. CMAJ. 2011;183(16):1851-1858. doi: 10.1503/cmaj.111152
- Review of adverse events