Stanford Health Care Antimicrobial Dosing Reference Guide
Stanford Health Care Antimicrobial Dosing Reference Guide
Stanford Health Care Antimicrobial Dosing Reference Guide
Intermittent
Drug CrCl > 50 mL/min CrCl 10 – 50 mL/min CrCl < 10 mL/min Hemodialysis (IHD) CRRT
Assumes thrice weekly dialysis
Usual dose:
CrCl < 10:
500 mg q8h CrCl 10 – 30:
500 mg q24h
or 875 mg q12h 500 mg q12h 500 mg q24h;
For q24h regimen, dose after
Amoxicillin/clavulanate CAP: 875 mg q12h IAI / Uncomplicated GNR
IAI / Uncomplicated GNR dialysis or administer No data
(PO)1,2,10–12 bacteremia (oral step-down
IAI / Uncomplicated GNR bacteremia (oral step-down additional dose at the end of
alternative):
bacteremia (oral step-down alternative): dialysis
up to 875 mg q24h
alternative): up to 875 mg q12h
up to 875 mg q8h
Amphotericin B
Liposomal1,2
3 – 5 mg/kg/day No change No change No change No change
(Consider adjusted BW
in obese)
Mild/uncomplicated: Mild/uncomplicated: CVVH: 2 g q8–12H
Mild/uncomplicated: Mild/uncomplicated:
1 g q6–8h 1 g q12h CVVHDF: 2 g q6–8h
1 – 2 g q6h 1 g q12h
Ampicillin (IV)1–3 Meningitis/endovascular Meningitis/endovascular Meningitis/endovascular
Meningitis/endovascular/PJI: Meningitis/endovascular/PJI:
/PJI: /PJI: /PJI:
2 g q4h 2 g q12–24h
2 g q6–12h 2 g q12–24h; or 1 g q8h 2 g q6h
1.5 – 3 g q12–24h
Ampicillin/sulbactam1–3,5 1.5 – 3 g q6h CrCl < 30: 1.5 – 3 g q12h CrCl < 15: 1.5 – 3 g q24h Dose daily, but after HD on HD 3 g q6–8h
days
CrCl
CMV induction CMV maintenance HSV
(mL/min/kg)
Foscarnet (IV)1,2,50–52
> 1.4 60 mg/kg q8h 90 mg/kg q12h 90 mg/kg q24h 120 mg/kg q24h 40 mg/kg q12h 40 mg/kg q8h
(Consider adjusted BW
in obese) > 1.0 – 1.4 45 mg/kg q8h 70 mg/kg q12h 70 mg/kg q24h 90 mg/kg q24h 30 mg/kg q12h 30 mg/kg q8h
> 0.8 – 1.0 50 mg/kg q12h 50 mg/kg q12h 50 mg/kg q24h 65 mg/kg q24h 20 mg/kg q12h 35 mg/kg q12h
> 0.6 – 0.8 40 mg/kg q12h 80 mg/kg q24h 80 mg/kg q48h 105 mg/kg q48h 35 mg/kg q24h 25 mg/kg q12h
Adj CrCl (mL/min/kg) > 0.5 – 0.6 60 mg/kg q24h 60 mg/kg q24h 60 mg/kg q48h 80 mg/kg q48h 25 mg/kg q24h 40 mg/kg q24h
≥ 0.4 – 0.5 50 mg/kg q24h 50 mg/kg q24h 50 mg/kg q48h 65 mg/kg q48h 20 mg/kg q24h 35 mg/kg q24h
< 0.4 Not recommended Not recommended Not recommended
IHD 45 – 60 mg/kg/dose post-HD only No data No data
CRRT No data
CMV CrCl >70* CrCl >50 CrCl >25 CrCl >10 CrCl <10
Ganciclovir (IV)1,2 5 mg/kg 2.5 mg/kg 2.5 mg/kg 1.25 mg/kg 1.25 mg/kg
Induction (I) I: 1.25 mg/kg post HD only I: 2.5 mg/kg q12–24h
(Consider adjusted BW q12h q12h q24h q24h 3x/week M: 0.625 mg/kg post HD only M: 1.25 – 2.5 mg/kg q24h
in obese) 5 mg/kg 2.5 mg/kg 1.25 mg/kg 0.625 mg/kg 0.625 mg/kg
Maintenance (M)
q24h q24h q24h q24h 3x/week
*Manufacturer’s CrCl cutoffs. Please refer to BMT protocols if applicable
Intermittent
Drug CrCl > 50 mL/min CrCl 10 – 50 mL/min CrCl < 10 mL/min Hemodialysis (IHD) CRRT
Assumes thrice weekly dialysis
CrCl > 60 CrCl 40 – 59 CrCl 20 – 39 CrCl < 20 IHD CRRT
1.7 mg/kg q8h 1.7 mg/kg q12h 1.7 mg/kg q24h
or or or 2 mg/kg 2 mg/kg loading 1.5 – 2.5
Gram negative 5 – 7 mg/kg q24h 5 – 7 mg/kg q36h CrCl > 30: 5 – 7 mg/kg q48h loading dose, dose, then 1.5 mg/kg
(high-dose (high-dose CrCl < 30: Not recommended then per level mg/kg post HD q24–48h
extended-interval) extended-interval) (high-dose extended-interval)
Gentamicin1,3,53 1 mg/kg q48–72h;
(Use adjusted BW in Gram positive 1 mg/kg load,consider redosing 1 mg/kg q24h,
obese) 1 mg/kg q8h** 1 mg/kg q12h 1 mg/kg q24h
synergy then by level when level then per level
< 1 mcg/L
See appendix for
Goal levels: Gram-negative infections: Goal peak for traditional dosing 4 – 8 mcg/mL; goal trough < 1 – 2 mcg/mL
complete guidelines
Gram-positive synergy: Goal peak 3 – 4 mcg/mL; goal trough < 1 mcg/mL
Timing of levels: Draw peak 30 minutes after completion of 3rd dose. Draw trough 30 minutes prior to 4th dose (For CrCl < 20 mL/min, may check levels
sooner than 3rd/4th dose)
For 7 mg/kg once-daily dosing, draw a single random level 8 – 12 hours after dose administration. Adjust based on Hartford nomogram
For HD, draw trough pre-HD (alternative: draw trough level 4-hr post-HD); and peak 30 minutes after end of each infusion
** Streptococci, Streptococcus gallolyticus (bovis), Streptococcus viridans endocarditis: optional dosing 3 mg/kg q24h for CrCl > 60 mL/min
** Staphylococci; Enterococcus spp (strains susceptible to PCN and gentamicin) endocarditis: optional dosing 3 mg/kg in 2 or 3 equally divided doses
Linezolid (IV/PO)1,2
600 mg q12h No change No change No change No change
(SHC Restriction)
CrCl > 50 CrCl 26 – 50 CrCl 10 – 25 CrCl < 10
500 mg q24h
Usual dose
Meropenem 1–4,54
(FN, PNA, 1 g q8h 1 g q12h 0.5 g q12h 0.5 g q24h 1 g q8h
CF/CNS: 1 g q24h
3-hr extended infusion Pseudomonas) CF/CNS: 2 g q12h
CF/Meningitis 2 g q8h 2 g q12h 1 g q12h 1 g q24h Dose daily, but after HD on HD
days
No change
Metronidazole (IV/PO)1,2 500 mg q6–8h 500 mg q8h 500 mg q6–8h
Severe hepatic impairment: can consider 500 mg q12h
1,2
Moxifloxacin (IV/PO) 400 mg IV/PO q24h No change No change No change No change
No change for renal impairment.
2 g q4h
Nafcillin1,2 Hepatic Impairment: No specific dose adjustment provided by manufacturer. Dosage adjustment may be necessary in the
Mild infections: 1 g q4h
setting of concomitant renal impairment; nafcillin primarily undergoes hepatic metabolism.
Prophylaxis:
CrCl ≥ 60 CrCl 30 – 60 CrCl 10 – 30 30 mg x 1, then 30 mg after
every other HD session Prophylaxis: 75 mg q24h
Oseltamivir (PO)1,2,55 Prophylaxis 75 mg q24h 30 mg q24h 30 mg q48h
Treatment: Treatment: 75 mg q12h
Treatment 75 mg q12h 30 mg q12h 30 mg q24h 30 mg x 1, then 30 mg post-
HD only
2 – 4 mu q4h
Mild: 0.5 – 1 mu q4–6h;
Dose range: 12 – 24 million or 1 – 2 mu q8–12h
Penicillin G (IV)1–3,5 units/day continuous infusion 2 – 3 mu q4h 1 – 2 mu q6h 4 mu q4–6h
Severe: 2 mu q4–6h;
or in divided doses every 4 to
or 4 mu q8–12h
6 hours
CrCl > 40 CrCl 20 – 40 CrCl < 20
Intermittent Dosing (30-minutes)
General 3.375 g q6h 2.25 g q6h 2.25 g q8h General: 2.25 g q12h
Severe/sepsis/CF/
4.5 g q6h 3.375 g q6h 2.25 g q6h 3.375 g q6h over 30-
nosocomial PNA
Severe infections: minutes
Piperacillin/tazobactam1 Extended-Infusion Dosing (4-hr infusion)
–4,56,57 3.375 g q12h over 4-hr
General, CF
Extended infusion for CrCl > 20: Extended infusion:
Pseudomonas, 3.375 g q12h over 4h
3.375 – 4.5 g q8h over 4h* alt: 2.25 g q8h 3.375 – 4.5 g q8h over 4-hr
nosocomial PNA:
*In select cases, higher piperacillin/tazobactam dosing may be warranted, e.g. sepsis,
critically ill patients with severe or deep-seated infections, infections with MIC > 16 mg/L,
obesity with weight > 120kg or BMI > 40, CrCl > 120 mL/min, or enhanced drug clearance
such as those with cystic fibrosis: consider doses of 4.5 g q8h (infused over 4 hours) or q6h.
Polymyxin B1,2,58,59 Dosing presented as units (10,000 units = 1 mg)
(SHC Restriction) 20,000 – 25,000 units/kg load x 1, then 12,500 – 15,000 units/kg q12h No data No change
(Use adjusted BW if
obese) (maximum: 25,000 units/kg/day)
Intermittent
Drug CrCl > 50 mL/min CrCl 10 – 50 mL/min CrCl < 10 mL/min Hemodialysis (IHD) CRRT
Assumes thrice weekly dialysis
No renal adjustment
Delayed-release tablet
Oral Suspension
/ Intravenous solution
Prophylaxis 200 mg q8h 300 mg q12h x 1 day,
Posaconazole (PO/IV)1,2
Treatment Usual dose: 200 mg q6–8h or 400 mg q12h then 300 mg q24h No change No change
(SHC Restriction [IV])
• Delayed-release tablet and oral suspension are not interchangeable
• Posaconazole levels shown to have great degree of interpatient variability. Consider
drawing a trough 4 – 7 days after initiating dose.
• Please refer to Antifungal TDM Guide
Usual Dose: 25 mg/kg q24h
(max dose: 2,000 mg/day)
Pyrazinamide (PO)1,2,47,48
(Use lean BW if obese) Lean body
Dose CrCl < 30: 25 mg/kg 3 times per week
(See footnote for lean BW weight No data
equation) 25 mg/kg 3 times per week Administer after HD only
40 – 55 kg 1,000 mg
56 – 75 kg 1,500 mg
76 – 90 kg 2,000 mg
Valganciclovir (PO)1,2 CrCl > 60 CrCl 40 – 59 CrCl 25 – 39 CrCl 10 – 24 CrCl < 10; IHD CRRT
Please refer to Induction (14-21 days) 900 mg q12h 450 mg q12h 450 mg q24h 450 mg q48h 200 mg 3x/week after HD only No data
transplant protocols if
applicable Maintenance/ prophylaxis 900 mg q24h 450 mg q24h 450 mg q48h 450 mg twice/week 100 mg 3x/week after HD only No data
Vancomycin (IV)1,2,65,66
(Use actual body See Vancomycin Dosing Protocol
weight)
Poor systemic absorption- used for the treatment of Clostridium difficile-associated diarrhea
Vancomycin PO1,2,67 Mild/moderate/severe: 125 mg PO q6h No change No change
Severe complicated (CDI-related septic shock, ileus, toxic megacolon): 500 mg PO q6h
IVPO conversion 1:1 (round to nearest tablet size- available in 200 mg and 50 mg tablets)
Voriconazole IV: 6 mg/kg IV q12h x 2,
(IV/PO)1,2,68,69 then 4 mg/kg IV q12h Caution with IV: accumulation of IV vehicle cyclodextrin occurs.
Consider PO if CrCl < 50 mL/min unless benefits justify risks of IV use.
(Dose by adjusted BW PO: 400 mg PO q12h x 2,
in obese) then 200 mg PO q12h Levels shown to have great degree of interpatient variability. Consider drawing a trough 4 – 7 days after new dose.
Please refer to Antifungal TDM Guide
Abbreviations: CAP = community acquired pneumonia; CRRT = continuous renal replacement therapy; FN = febrile neutropenia; HD = hemodialysis; LD = loading dose; MU = million
units; PCP = pneumocystis jiroveci pneumonia; PNA = pneumonia; SCr = serum creatinine; TB = tuberculosis; TMP = trimethoprim; UF = ultrafiltration
CRRT dosing: doses listed are for CVVHDF and CVVHD modalities, which are the most common modes at SHC. Note that these are generally higher than doses used in CVVH.
LBW (men) = (1.10 x Weight(kg)) - 128 x (Weight2/(100 x Height(m))2)
LBW (women) = (1.07 x Weight(kg)) - 148 x (Weight2/(100 x Height(m))2)
LBW online calculator: http://www.empr.com/medical-calculators/lean-body-weight-calculator/article/170219/
References:
1. Lexicomp Online. Accessed April 9, 2017. http://online.lexi.com
2. MICROMEDEX®. Accessed April 9, 2017. http://www.micromedexsolutions.com.laneproxy.stanford.edu/micromedex2/librarian
3. Heintz BH, Matzke GR, Dager WE. Antimicrobial Dosing Concepts and Recommendations for Critically Ill Adult Patients Receiving Continuous Renal Replacement Therapy or
Intermittent Hemodialysis. Pharmacother J Hum Pharmacol Drug Ther. 2009;29. doi:10.1592/phco.29.5.562
4. Trotman RL, Williamson JC, Shoemaker DM, Salzer WL. Antibiotic Dosing in Critically Ill Adult Patients Receiving Continuous Renal Replacement Therapy. Clin Infect Dis.
2005;41(8):1159-1166. doi:10.1086/444500
5. Aronoff G, Bennett W, Berns J, et al. Drug Prescribing in Renal Failure. 5th ed. American College of Physicians; 2007.
6. Turner RB, Cumpston A, Sweet M, et al. Prospective, Controlled Study of Acyclovir Pharmacokinetics in Obese Patients. Antimicrob Agents Chemother. 2016;60. doi:10.1128/aac.02010-
15
7. Tomblyn M, Chiller T, Einsele H, et al. Guidelines for Preventing Infectious Complications among Hematopoietic Cell Transplantation Recipients: A Global Perspective. Biol Blood
Marrow Transplant. 2009;15(10):1143-1238. doi:10.1016/j.bbmt.2009.06.019
8. Roger C, Wallis SC, Muller L, et al. Influence of Renal Replacement Modalities on Amikacin Population Pharmacokinetics in Critically Ill Patients on Continuous Renal Replacement
Therapy. Antimicrob Agents Chemother. 2016;60. doi:10.1128/aac.00828-16
9. Taccone FS, Backer D de, Laterre P-F, et al. Pharmacokinetics of a loading dose of amikacin in septic patients undergoing continuous renal replacement therapy. Int J Antimicrob Agents.
2011;37. doi:10.1016/j.ijantimicag.2011.01.026
10. Mora Lopez L, Serra Pla S, Serra-Aracil X, Ballesteros E, Navarro S. Application of a modified Neff classification to patients with uncomplicated diverticulitis. Colorectal Dis.
2013;15(11):1442-1447. doi:10.1111/codi.12449
11. Biondo S, Golda T, Kreisler E, et al. Outpatient Versus Hospitalization Management for Uncomplicated Diverticulitis: A Prospective, Multicenter Randomized Clinical Trial (DIVER
Trial). Ann Surg. 2014;259(1):38-44. doi:10.1097/SLA.0b013e3182965a11
12. Mora-López L, Ruiz-Edo N, Estrada-Ferrer O, et al. Efficacy and Safety of Nonantibiotic Outpatient Treatment in Mild Acute Diverticulitis (DINAMO-study): A Multicentre, Randomised,
Open-label, Noninferiority Trial. Ann Surg. 2021;274(5):e435. doi:10.1097/SLA.0000000000005031
13. Gerig JS, Bolton ND, Swabb EA, Scheld WM, Bolton WK. Effect of hemodialysis and peritoneal dialysis on aztreonam pharmacokinetics. Kidney Int. 1984;26. doi:10.1038/ki.1984.174
14. Gustot T, ter Heine R, Brauns E, Cotton F, Jacobs F, Brüggemann RJ. Caspofungin dosage adjustments are not required for patients with Child–Pugh B or C cirrhosis. J Antimicrob
Chemother. 2018;73(9):2493-2496. doi:10.1093/jac/dky189
15. Roger C, Wallis SC, Muller L, et al. Caspofungin Population Pharmacokinetics in Critically Ill Patients Undergoing Continuous Veno-Venous Haemofiltration or Haemodiafiltration. Clin
Pharmacokinet. 2017;56(9):1057-1068. doi:10.1007/s40262-016-0495-z
16. Pappas PG, Kauffman CA, Andes DR, et al. Clinical Practice Guideline for the Management of Candidiasis: 2016 Update by the Infectious Diseases Society of America. Clin Infect Dis Off
Publ Infect Dis Soc Am. 2016;62(4):e1-50. doi:10.1093/cid/civ933
17. Stryjewski ME, Szczech LA, Benjamin DK, et al. Use of Vancomycin or First-Generation Cephalosporins for the Treatment of Hemodialysis-Dependent Patients with Methicillin-
Susceptible Staphylococcus aureus Bacteremia. Clin Infect Dis. 2007;44. doi:10.1086/510386
18. Crandon JL, Bulik CC, Kuti JL, Nicolau DP. Clinical Pharmacodynamics of Cefepime in Patients Infected with Pseudomonas aeruginosa. Antimicrob Agents Chemother. 2010;54.
doi:10.1128/AAC.01183-09
19. Bauer KA, West JE, O’Brien JM, Goff DA. Extended-infusion cefepime reduces mortality in patients with Pseudomonas aeruginosa infections. Antimicrob Agents Chemother. 2013;57.
doi:10.1128/AAC.02365-12
20. Hoff BM, Maker JH, Dager WE, Heintz BH. Antibiotic Dosing for Critically Ill Adult Patients Receiving Intermittent Hemodialysis, Prolonged Intermittent Renal Replacement Therapy,
and Continuous Renal Replacement Therapy: An Update. Ann Pharmacother. 2020;54(1):43-55. doi:10.1177/1060028019865873
21. Vidaillac C, Leonard SN, Rybak MJ. In vitro activity of ceftaroline against methicillin-resistant Staphylococcus aureus and heterogeneous vancomycin-intermediate S. aureus in a hollow
fiber model. Antimicrob Agents Chemother. 2009;53(11):4712-4717. doi:10.1128/AAC.00636-09
22. Loo AS, Neely M, Anderson EJ, Ghossein C, McLaughlin MM, Scheetz MH. Pharmacodynamic target attainment for various ceftazidime dosing schemes in high-flux hemodialysis.
Antimicrob Agents Chemother. 2013;57(12):5854-5859. doi:10.1128/AAC.00474-13
23. Wenzler E, Bunnell KL, Bleasdale SC, Benken S, Danziger LH, Rodvold KA. Pharmacokinetics and Dialytic Clearance of Ceftazidime-Avibactam in a Critically Ill Patient on Continuous
Venovenous Hemofiltration. Antimicrob Agents Chemother. 2017;61(7). doi:10.1128/AAC.00464-17
24. Soukup P, Faust AC, Edpuganti V, Putnam WC, McKinnell JA. Steady-State Ceftazidime-Avibactam Serum Concentrations and Dosing Recommendations in a Critically Ill Patient Being
Treated for Pseudomonas aeruginosa Pneumonia and Undergoing Continuous Venovenous Hemodiafiltration. Pharmacother J Hum Pharmacol Drug Ther. 2019;39(12):1216-1222.
doi:10.1002/phar.2338
25. Pistolesi V, Morabito S, Di Mario F, Regolisti G, Cantarelli C, Fiaccadori E. A Guide to Understanding Antimicrobial Drug Dosing in Critically Ill Patients on Renal Replacement Therapy.
Antimicrob Agents Chemother. 2019;63(8). doi:10.1128/AAC.00583-19
26. Li L, Li X, Xia Y, et al. Recommendation of Antimicrobial Dosing Optimization During Continuous Renal Replacement Therapy. Front Pharmacol. 2020;11.
doi:10.3389/fphar.2020.00786
27. Bremmer DN, Nicolau DP, Burcham P, Chunduri A, Shidham G, Bauer KA. Ceftolozane/Tazobactam Pharmacokinetics in a Critically Ill Adult Receiving Continuous Renal Replacement
Therapy. Pharmacother J Hum Pharmacol Drug Ther. 2016;36(5):e30-e33. doi:10.1002/phar.1744
28. Oliver WD, Heil EL, Gonzales JP, et al. Ceftolozane-Tazobactam Pharmacokinetics in a Critically Ill Patient on Continuous Venovenous Hemofiltration. Antimicrob Agents Chemother.
2016;60. doi:10.1128/aac.02608-15
29. Aguilar G, Ferriols R, Martínez-Castro S, et al. Optimizing ceftolozane-tazobactam dosage in critically ill patients during continuous venovenous hemodiafiltration. Crit Care. 2019;23.
doi:10.1186/s13054-019-2434-5
30. Laville M, Mercatello A, Freney J, et al. Pharmacokinetics of ceftriaxone in hemodialysis. Pathol Biol (Paris). 1987;35(5 Pt 2):719-723.
31. Stevens DL, Bisno AL, Chambers HF, et al. Practice Guidelines for the Diagnosis and Management of Skin and Soft Tissue Infections: 2014 Update by the Infectious Diseases Society of
America. Clin Infect Dis. 2014;59. doi:10.1093/cid/ciu296
32. Roger C, Wallis SC, Louart B, et al. Comparison of equal doses of continuous venovenous haemofiltration and haemodiafiltration on ciprofloxacin population pharmacokinetics in critically
ill patients. J Antimicrob Chemother. 2016;71(6):1643-1650. doi:10.1093/jac/dkw043
33. Nation RL, Garonzik SM, Thamlikitkul V, et al. Dosing Guidance for Intravenous Colistin in Critically Ill Patients. Clin Infect Dis. 2017;64(5):565-571. doi:10.1093/cid/ciw839
34. Plachouras D, Karvanen M, Friberg LE, et al. Population pharmacokinetic analysis of colistin methanesulfonate and colistin after intravenous administration in critically ill patients with
infections caused by gram-negative bacteria. Antimicrob Agents Chemother. 2009;53(8):3430-3436. doi:10.1128/AAC.01361-08
35. Dalfino L, Puntillo F, Mosca A, et al. High-dose, extended-interval colistin administration in critically ill patients: is this the right dosing strategy? A preliminary study. Clin Infect Dis Off
Publ Infect Dis Soc Am. 2012;54(12):1720-1726. doi:10.1093/cid/cis286
36. Dvorchik BH, Damphousse D. The pharmacokinetics of daptomycin in moderately obese, morbidly obese, and matched nonobese subjects. J Clin Pharmacol. 2005;45(1):48-56.
doi:10.1177/0091270004269562
37. Pai MP, Norenberg JP, Anderson T, et al. Influence of morbid obesity on the single-dose pharmacokinetics of daptomycin. Antimicrob Agents Chemother. 2007;51(8):2741-2747.
doi:10.1128/AAC.00059-07
38. Haselden M, Leach M, Bohm N. Daptomycin dosing strategies in patients receiving thrice-weekly intermittent hemodialysis. Ann Pharmacother. 2013;47(10):1342-1347.
doi:10.1177/1060028013503110
39. Patel N, Cardone K, Grabe DW, et al. Use of pharmacokinetic and pharmacodynamic principles to determine optimal administration of daptomycin in patients receiving standardized
thrice-weekly hemodialysis. Antimicrob Agents Chemother. 2011;55(4):1677-1683. doi:10.1128/AAC.01224-10
40. Falcone M, Russo A, Cassetta MI, et al. Daptomycin serum levels in critical patients undergoing continuous renal replacement. J Chemother Florence Italy. 2012;24(5):253-256.
doi:10.1179/1973947812Y.0000000033
41. Preiswerk B, Rudiger A, Fehr J, Corti N. Experience with daptomycin daily dosing in ICU patients undergoing continuous renal replacement therapy. Infection. 2013;41(2):553-557.
doi:10.1007/s15010-012-0300-3
42. Xu X, Khadzhynov D, Peters H, et al. Population pharmacokinetics of daptomycin in adult patients undergoing continuous renal replacement therapy. Br J Clin Pharmacol.
2017;83(3):498-509. doi:10.1111/bcp.13131
43. Diolez J, Venisse N, Belmouaz S, Bauwens M-A, Bridoux F, Beraud G. Pilot Pharmacokinetic Study of High-Dose Daptomycin in Hemodialysis Patients With Infected Medical Devices.
Am J Kidney Dis Off J Natl Kidney Found. 2017;70(5):732-734. doi:10.1053/j.ajkd.2017.05.011
44. Geerlings CJC, de Man P, Rietveld AP, Touw DJ, Cohen Tervaert JW. A practical thrice weekly Ertapenem dosage regime for chronic hemodialysis patients? Clin Nephrol.
2013;80(4):312. doi:10.5414/cn108071
45. Hsaiky LM, Salinitri FD, Wong J, et al. Pharmacokinetics and investigation of optimal dose ertapenem in intermittent hemodialysis patients. Nephrol Dial Transplant. 2019;34(10):1766-
1772. doi:10.1093/ndt/gfy166
46. Ueng Y-F, Wang H-J, Wu S-C, Ng Y-Y. A Thrice-Weekly Ertapenem Regimen Is Practical for Hemodialysis Patients. Antimicrob Agents Chemother. 2019;63(12).
doi:10.1128/AAC.01427-19
47. Drug-Resistant Tuberculosis: A Survival Guide for Clinicians, 3rd edition | Curry International Tuberculosis Center. Accessed April 10, 2017.
http://www.currytbcenter.ucsf.edu/products/cover-pages/drug-resistant-tuberculosis-survival-guide-clinicians-3rd-edition
48. Nahid P, Dorman SE, Alipanah N, et al. Official American Thoracic Society/Centers for Disease Control and Prevention/Infectious Diseases Society of America Clinical Practice
Guidelines: Treatment of Drug-Susceptible Tuberculosis. Clin Infect Dis Off Publ Infect Dis Soc Am. 2016;63(7):e147-195. doi:10.1093/cid/ciw376
49. Muilwijk EW, Lange DW de, Schouten JA, et al. Suboptimal Dosing of Fluconazole in Critically Ill Patients: Time To Rethink Dosing. Antimicrob Agents Chemother. 2020;64(10).
doi:10.1128/AAC.00984-20
50. Aweeka FT, Jacobson MA, Martin-Munley S, et al. Effect of renal disease and hemodialysis on foscarnet pharmacokinetics and dosing recommendations. J Acquir Immune Defic Syndr
Hum Retrovirology Off Publ Int Retrovirology Assoc. 1999;20(4):350-357.
51. Jayasekara D, Aweeka FT, Rodriguez R, Kalayjian RC, Humphreys MH, Gambertoglio JG. Antiviral therapy for HIV patients with renal insufficiency. J Acquir Immune Defic Syndr 1999.
1999;21(5):384-395.
52. MacGregor RR, Graziani AL, Weiss R, Grunwald JE, Gambertoglio JG. Successful foscarnet therapy for cytomegalovirus retinitis in an AIDS patient undergoing hemodialysis: rationale
for empiric dosing and plasma level monitoring. J Infect Dis. 1991;164(4):785-787.
53. Nicolau DP, Freeman CD, Belliveau PP, Nightingale CH, Ross JW, Quintiliani R. Experience with a once-daily aminoglycoside program administered to 2,184 adult patients. Antimicrob
Agents Chemother. 1995;39(3):650-655.
54. Kuti JL, Dandekar PK, Nightingale CH, Nicolau DP. Use of Monte Carlo simulation to design an optimized pharmacodynamic dosing strategy for meropenem. J Clin Pharmacol.
2003;43(10):1116-1123. doi:10.1177/0091270003257225
55. Robson R, Buttimore A, Lynn K, Brewster M, Ward P. The pharmacokinetics and tolerability of oseltamivir suspension in patients on haemodialysis and continuous ambulatory peritoneal
dialysis. Nephrol Dial Transplant Off Publ Eur Dial Transpl Assoc - Eur Ren Assoc. 2006;21(9):2556-2562. doi:10.1093/ndt/gfl267
56. Lodise TP, Lomaestro B, Drusano GL. Piperacillin-tazobactam for Pseudomonas aeruginosa infection: clinical implications of an extended-infusion dosing strategy. Clin Infect Dis Off
Publ Infect Dis Soc Am. 2007;44(3):357-363. doi:10.1086/510590
57. Patel N, Scheetz MH, Drusano GL, Lodise TP. Identification of optimal renal dosage adjustments for traditional and extended-infusion piperacillin-tazobactam dosing regimens in
hospitalized patients. Antimicrob Agents Chemother. 2010;54(1):460-465. doi:10.1128/AAC.00296-09
58. Sandri AM, Landersdorfer CB, Jacob J, et al. Population pharmacokinetics of intravenous polymyxin B in critically ill patients: implications for selection of dosage regimens. Clin Infect
Dis Off Publ Infect Dis Soc Am. 2013;57(4):524-531. doi:10.1093/cid/cit334
59. Tsuji BT, Pogue JM, Zavascki AP, et al. International Consensus Guidelines for the Optimal Use of the Polymyxins: Endorsed by the American College of Clinical Pharmacy (ACCP),
European Society of Clinical Microbiology and Infectious Diseases (ESCMID), Infectious Diseases Society of America (IDSA), International Society for Anti-infective Pharmacology
(ISAP), Society of Critical Care Medicine (SCCM), and Society of Infectious Diseases Pharmacists (SIDP). Pharmacother J Hum Pharmacol Drug Ther. 2019;39(1):10-39.
doi:10.1002/phar.2209
60. Baddour LM, Wilson WR, Bayer AS, et al. Infective Endocarditis in Adults: Diagnosis, Antimicrobial Therapy, and Management of Complications: A Scientific Statement for Healthcare
Professionals From the American Heart Association. Circulation. 2015;132(15):1435-1486. doi:10.1161/CIR.0000000000000296
61. Osmon DR, Berbari EF, Berendt AR, et al. Diagnosis and management of prosthetic joint infection: clinical practice guidelines by the Infectious Diseases Society of America. Clin Infect
Dis Off Publ Infect Dis Soc Am. 2013;56(1):e1-e25. doi:10.1093/cid/cis803
62. Berbari EF, Kanj SS, Kowalski TJ, et al. 2015 Infectious Diseases Society of America (IDSA) Clinical Practice Guidelines for the Diagnosis and Treatment of Native Vertebral
Osteomyelitis in Adults. Clin Infect Dis Off Publ Infect Dis Soc Am. 2015;61(6):e26-46. doi:10.1093/cid/civ482
63. Flanagan S, Minassian SL, Morris D, et al. Pharmacokinetics of tedizolid in subjects with renal or hepatic impairment. Antimicrob Agents Chemother. 2014;58(11):6471-6476.
doi:10.1128/AAC.03431-14
64. Nahata MC. Dosage regimens of trimethoprim/sulfamethoxazole (TPM/SMX) in patients with renal dysfunction. Ann Pharmacother. 1995;29(12):1300.
65. Rybak M, Lomaestro B, Rotschafer JC, et al. Therapeutic monitoring of vancomycin in adult patients: a consensus review of the American Society of Health-System Pharmacists, the
Infectious Diseases Society of America, and the Society of Infectious Diseases Pharmacists. Am J Health-Syst Pharm AJHP Off J Am Soc Health-Syst Pharm. 2009;66(1):82-98.
doi:10.2146/ajhp080434
66. Liu C, Bayer A, Cosgrove SE, et al. Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in
adults and children. Clin Infect Dis Off Publ Infect Dis Soc Am. 2011;52(3):e18-55. doi:10.1093/cid/ciq146
67. Cohen SH, Gerding DN, Johnson S, et al. Clinical Practice Guidelines for Clostridium difficile Infection in Adults: 2010 Update by the Society for Healthcare Epidemiology of America
(SHEA) and the Infectious Diseases Society of America (IDSA). Infect Control Hosp Epidemiol. 2010;31(5):431-455. doi:10.1086/651706
68. Koselke E, Kraft S, Smith J, Nagel J. Evaluation of the effect of obesity on voriconazole serum concentrations. J Antimicrob Chemother. 2012;67(12):2957-2962. doi:10.1093/jac/dks312
69. Davies-Vorbrodt S, Ito JI, Tegtmeier BR, Dadwal SS, Kriengkauykiat J. Voriconazole serum concentrations in obese and overweight immunocompromised patients: a retrospective review.
Pharmacotherapy. 2013;33(1):22-30. doi:10.1002/phar.1156
A. Original Author/Date
Department of Pharmacy; 07/1998
B. Gatekeeper
Stanford Antimicrobial Stewardship Safety and Sustainability Program
D. Revision/Review History
Deepak Sisodiya, PharmD; 04/2005
Maggie Cudny, PharmD, BCOP; 04/2007, 01/2009
Katherine Miller, PharmD; 01/2009
Sean Carlton, PharmD, BCPS; 03/2010
Emily Mui, PharmD, BCIDP; 11/2010, 03/2011, 05/2012, 05/2013, 01/2014, 03/2017, 02/2019, 07/2019, 08/2019, 10/2019, 01/2020, 05/2020, 09/2020,
12/2021
Lina Meng, PharmD, BCPS, BCCCP; 11/2010, 03/2011, 03/2017, 08/2019, 10/2019, 05/2020, 09/2020, 12/2021
Marisa Holubar, MD; 03/2017
Stan Deresinski, MD; 03/2017
Will Alegria, PharmD; 08/2019, 01/2020, 05/2020, 09/2020, 12/2021
David Ha, PharmD; 01/2020, 05/2020, 09/2020, 12/2021
E. Approvals
Antimicrobial Subcommittee 09/2004, 04/2007, 01/2009, 11/2010, 03/2011, 05/2012, 05/2013, 01/2014, 03/2017, 07/2019, 10/2019; 01/2020, 09/2020,
08/2021,12/2021
Pharmacy & Therapeutics Committee 04/2007, 02/2009, 04/2010, 05/2011, 08/2012, 09/2012, 08/2013, 02/2014, 04/2017, 11/2019; 02/2020, 10/2020,
09/2021