Comprehensive guidance for antibiotic dosing in obese adults: 2022 update.


Journal

Pharmacotherapy
ISSN: 1875-9114
Titre abrégé: Pharmacotherapy
Pays: United States
ID NLM: 8111305

Informations de publication

Date de publication:
03 2023
Historique:
revised: 19 01 2023
received: 31 10 2022
accepted: 23 01 2023
pubmed: 27 1 2023
medline: 16 3 2023
entrez: 26 1 2023
Statut: ppublish

Résumé

Drug dosing in obese patients continues to be challenging due to a lack of high-quality evidence to guide dosing recommendations. We first published guidance for antibiotic dosing in obese adults in 2017, in which we critically reviewed articles identified from a broad search strategy to develop dosing recommendations for 35 antimicrobials. In this updated narrative review, we searched Pubmed, Web of Science, and the Cochrane Library using Medical Subject Headings including anti-infectives, specific generic antimicrobial names, obese, pharmacokinetics, and others. We reviewed 393 articles, cross-referenced select cited references, and when applicable, referenced drug databases, package inserts, and clinical trial data to update dosing recommendations for 41 antimicrobials. Most included articles were pharmacokinetic studies, other less frequently included articles were clinical studies (mostly small, retrospective), case reports, and very rarely, guidelines. Pharmacokinetic changes are frequently reported, can be variable, and sometimes conflicting in this population, and do not always translate to a documented difference in clinical outcomes, yet are used to inform dosing strategies. Extended infusions, high doses, and therapeutic drug monitoring remain important strategies to optimize dosing in this population. Additional studies are needed to clinically validate proposed dosing strategies, clarify optimal body size descriptors, dosing weight scalars, and estimation method of renal function in obese patients.

Identifiants

pubmed: 36703246
doi: 10.1002/phar.2769
doi:

Substances chimiques

Anti-Bacterial Agents 0
Anti-Infective Agents 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

226-246

Informations de copyright

© 2023 Pharmacotherapy Publications, Inc.

Références

Meng L, Mui E, Holubar MK, Deresinski SC. Comprehensive guidance for antibiotic dosing in obese adults. Pharmacotherapy. 2017;37(11):1415-1431.
Pai MP. Antimicrobial dosing in specific populations and novel clinical methodologies: obesity. Clin Pharmacol Ther. 2021;109(4):942-951.
Alobaid AS, Hites M, Lipman J, Taccone FS, Roberts JA. Effect of obesity on the pharmacokinetics of antimicrobials in critically ill patients: a structured review. Int J Antimicrob Agents. 2016;47(4):259-268.
Hanley MJ, Abernethy DR, Greenblatt DJ. Effect of obesity on the pharmacokinetics of drugs in humans. Clin Pharmacokinet. 2010;49(2):71-87.
Rowland M, Tozer TN. Clinical Pharmacokinetics: Concepts and Applications. Williams & Wilkins; 1995.
Ryu H, Mohayya S, Hong T, et al. Safety and effectiveness of high-dose cefazolin in patients with high body weight: a retrospective cohort study. Open Forum Infect Dis. 2022;9(4):Ofac105.
Kees MG, Weber S, Kees F, Horbach T. Pharmacokinetics of moxifloxacin in plasma and tissue of morbidly obese patients. J Antimicrob Chemother. 2011;66(10):2330-2335.
Pai MP, Rodvold KA. Aminoglycoside dosing in patients by kidney function and area under the curve: the Sawchuk-Zaske dosing method revisited in the era of obesity. Diagn Microbiol Infect Dis. 2014;78(2):178-187.
Bland CM, Pai MP, Lodise TP. Reappraisal of contemporary pharmacokinetic and pharmacodynamic principles for informing aminoglycoside dosing. Pharmacotherapy: J Human Pharmacol Drug Therapy. 2018;38(12):1229-1238.
Cox KK, Alexander B, Livorsi DJ, Heintz BH. Clinical outcomes in patients hospitalized with cellulitis treated with oral clindamycin and trimethoprim/sulfamethoxazole: the role of weight-based dosing. J Infect. 2017;75(6):486-492.
Crass R, Dunn R, Hong J, Krop L, Pai M. Dosing vancomycin in the super obese: less is more. J Antimicrob Chemother. 2018;73(11):3081-3086.
Hong J, Krop LC, Johns T, Pai MP. Individualized vancomycin dosing in obese patients: a two-sample measurement approach improves target attainment. Pharmacotherapy. 2015;35(5):455-463.
Soule AF, Green SB, Blanchette LM. Clinical efficacy of 12-H metronidazole dosing regimens in patients with anaerobic or mixed anaerobic infections. Therapeutic Adv Infect. 2018;5(3):57-62.
Dorn C, Petroff D, Stoelzel M, et al. Perioperative administration of cefazolin and metronidazole in obese and non-obese patients: a pharmacokinetic study in plasma and interstitial fluid. J Antimicrob Chemother. 2021;76(8):2114-2120.
Busse D, Simon P, Petroff D, et al. High-dosage fosfomycin results in adequate plasma and target-site exposure in morbidly obese and nonobese nonhyperfiltration patients. Antimicrobial Agents Chemother. 2022;66(6):e02302-21. doi: 10.1128/aac.02302-21
File TM, Beegle S, Crandon J, et al. Lefamulin efficacy in adults with community-acquired bacterial pneumonia (CABP) is unaffected by obesity: pooled analysis of the Lefamulin phase 3 clinical trial program. Chest. 2022;162(4):A307-A308.
Fratoni AJ, Nicolau DP, Kuti JL. A guide to therapeutic drug monitoring of Β-lactam antibiotics. Pharmacotherapy. 2021;41(2):220-233.
Hagel S, Bach F, Brenner T, et al. Effect of therapeutic drug monitoring-based dose optimization of piperacillin/tazobactam on sepsis-related organ dysfunction in patients with sepsis: a randomized controlled trial. Intensive Care Med. 2022;48(3):311-321.
Roberts JA, Paul SK, Akova M, et al. DALI: defining antibiotic levels in intensive care unit patients: are current -lactam antibiotic doses sufficient for critically ill patients? Clin Infect Dis. 2014;58(8):1072-1083.
De Waele JJ, Carrette S, Carlier M, et al. Therapeutic drug monitoring-based dose optimisation of piperacillin and meropenem: a randomised controlled trial. Intensive Care Med. 2014;40(3):380-387.
Abdul-Aziz MH, Alffenaar JWC, Bassetti M, et al. Antimicrobial therapeutic drug monitoring in critically ill adult patients: a position paper. Intensive Care Med. 2020;46(6):1127-1153.
Guilhaumou R, Benaboud S, Bennis Y, et al. Optimization of the treatment with Beta-lactam antibiotics in critically ill patients-guidelines from the French society of pharmacology and therapeutics (Société Française De Pharmacologie et Thérapeutique-SFPT) and the French society of Anaesthesia and intensive care medicine (Société Française d'Anesthésie et Réanimation-SFAR). Crit Care. 2019;23(1):104.
Kunz Coyne AJ, Alshaer M, Casapao AM, et al. Effectiveness and safety of Beta-lactam antibiotics with and without therapeutic drug monitoring in patients with pseudomonas aeruginosa pneumonia or bloodstream infection. Antimicrob Agents Chemother. 2022;66(10):E00646-E00622.
Longo C, Bartlett G, Macgibbon B, et al. The effect of obesity on antibiotic treatment failure: a historical cohort study. Pharmacoepidemiol Drug Saf. 2013;22(9):970-976.
Soares ALPPDP, Montanha MC, Alcantara CDS, et al. Pharmacokinetics of amoxicillin in obese and nonobese subjects. Br J Clin Pharmacol. 2021;87(8):3227-3233.
Rocha MBS, De Nucci G, Lemos FN, et al. Impact of bariatric surgery on the pharmacokinetics parameters of amoxicillin. Obes Surg. 2019;29(3):917-927.
Mellon G, Hammas K, Burdet C, et al. Population pharmacokinetics and dosing simulations of amoxicillin in obese adults receiving co-amoxiclav. J Antimicrob Chemother. 2020;75(12):3611-3618.
CLSI M100-ED32:2022. Performance Standards for Antimicrobial Susceptibility Testing, 32nd Edition. [Cited 2022 Sep 13]. Available From: http://Em100.Edaptivedocs.Net/Getdoc.Aspx?Doc=CLSI%20M100%20ED32:2022&Sbssok=CLSI%20M100%20ED32:2022%20TABLE%202A
Jung B, Mahul M, Breilh D, et al. Repeated piperacillin-tazobactam plasma concentration measurements in severely obese versus nonobese critically ill septic patients and the risk of under- and overdosing. Crit Care Med. 2017;45(5):E470-E478.
Alobaid AS, Wallis SC, Jarrett P, et al. Population pharmacokinetics of piperacillin in nonobese, obese, and morbidly obese critically ill patients. Antimicrob Agents Chemother. 2017;61(3):E01276-E01216.
Hites M, Taccone FS, Wolff F, et al. Broad-spectrum Β-lactams in obese non-critically ill patients. Nutr Diabetes. 2014;4(6):E119.
Hites M, Taccone FS, Wolff F, et al. Case-control study of drug monitoring of Β-lactams in obese critically ill patients. Antimicrob Agents Chemother. 2013;57(2):708-715.
Chung EK, Cheatham SC, Fleming MR, Healy DP, Shea KM, Kays MB. Population pharmacokinetics and pharmacodynamics of piperacillin and tazobactam administered by prolonged infusion in obese and nonobese patients. J Clin Pharmacol. 2015;55(8):899-908.
Cheatham SC, Fleming MR, Healy DP, et al. Steady-state pharmacokinetics and pharmacodynamics of piperacillin and tazobactam administered by prolonged infusion in obese patients. Int J Antimicrob Agents. 2013;41(1):52-56.
Santibañez M, Bunnell K, Harrington A, Bleasdale S, Wenzler E. Association between estimated pharmacokinetic/pharmacodynamic predictions of efficacy and observed clinical outcomes in obese and nonobese patients with enterobacteriaceae bloodstream infections. Open Forum Infect Dis. 2019;6(10):Ofz400.
Veillette JJ, Winans SA, Maskiewicz VK, Truong J, Jones RN, Forland SC. Pharmacokinetics and pharmacodynamics of high-dose piperacillin-tazobactam in obese patients. Eur J Drug Metab Pharmacokinet. 2021;46(3):385-394.
Roberts JA, Udy AA, Jarrett P, et al. Plasma and target-site subcutaneous tissue population pharmacokinetics and dosing simulations of cefazolin in post-trauma critically ill patients. J Antimicrob Chemother. 2015;70(5):1495-1502.
Zeller V, Durand F, Kitzis MD, et al. Continuous cefazolin infusion to treat bone and joint infections: clinical efficacy, feasibility, safety, and serum and bone concentrations. Antimicrob Agents Chemother. 2009;53(3):883-887.
Bratzler DW, Dellinger EP, Olsen KM, et al. Clinical practice guidelines for antimicrobial prophylaxis in surgery. Am J Health Syst Pharm. 2013;70(3):195-283.
Poltak J, Connors C, Wungwattana M, Nicolau D, Mercuro NJ, Liu J. Pharmacokinetics of cefazolin in patients with obesity undergoing surgery requiring cardiopulmonary bypass. J Cardiothorac Vasc Anesth. 2022;36(8, Part B):2942-2947.
Alrammaal H, Abduljalil K, Morton V, et al. Application of a physiologically based pharmacokinetic model to predict cefazolin and cefuroxime disposition In obese pregnant women undergoing caesarean section. Pharmaceutics. 2022;14(6):1162. doi: 10.3390/pharmaceutics14061162
Grupper M, Nicolau DP. Obesity and skin and soft tissue infections: how to optimize antimicrobial usage for prevention and treatment? Curr Opin Infect Dis. 2017;30(2):180-191.
Ryan RL, Jackson D, Hopkins G, et al. Plasma and interstitial fluid pharmacokinetics of prophylactic cefazolin in elective bariatric surgery patients. Antimicrob Agents Chemother. 2022;66(7):E0041922.
Tchaick RM, Sá MPBO, Figueira FRDM, Paz KC, ÁAB F, Moraes FRDN. Cefazolin concentration in the mediastinal adipose tissue of patients undergoing cardiac surgery. Braz J Cardiovasc Surg (Torino). 2017;32(4):239-244.
Coates M, Shield A, Peterson G, Hussain Z. Prophylactic cefazolin dosing in obesity-a systematic review. Obes Surg. 2022;32(9):3138-3149.
Hussain Z, Curtain C, Mirkazemi C, Gadd K, Peterson GM, Zaidi STR. Prophylactic cefazolin dosing and surgical site infections: does the dose matter in obese patients? Obes Surg. 2019;29(1):159-165.
Morris AJ, Roberts SA, Grae N, Frampton CM. Surgical site infection rate is higher following hip and knee arthroplasty when cefazolin is underdosed. Am J Health Syst Pharm. 2020;77(6):434-440.
Rondon AJ, Kheir MM, Tan TL, Shohat N, Greenky MR, Parvizi J. Cefazolin prophylaxis for total joint arthroplasty: obese patients are frequently underdosed and at increased risk of periprosthetic joint infection. J Arthroplasty. 2018;33(11):3551-3554.
Barber KE, Loper JT, Morrison AR, Stover KR, Wagner JL. Impact of obesity on ceftriaxone efficacy. Diseases. 2020;8(3):27.
Pinner NA, Tapley NG, Barber KE, Stover KR, Wagner JL. Effect of obesity on clinical failure of patients treated with Β-lactams. Open Forum Infect Dis. 2021;8(8):Ofab212.
Xiao AJ, Huntington JA, Long J, Caro L. Ceftolozane/tazobactam dose regimens in severely/morbidly obese patients with complicated intra-abdominal infection or complicated urinary tract infection. Int J Antimicrob Agents. 2018 Sep 1;52(3):324-330.
Justo JA, Mayer SM, Pai MP, et al. Pharmacokinetics of ceftaroline in normal body weight and obese (classes I, II, and III) healthy adult subjects. Antimicrob Agents Chemother. 2015;59(7):3956-3965.
Wilcox M, Yan JL, Gonzalez PL, Dryden M, Stone GG, Kantecki M. Impact of underlying comorbidities on outcomes of patients treated with Ceftaroline Fosamil for complicated skin and soft tissue infections: pooled results from three phase III randomized clinical trials. Infect Dis Ther. 2022;11(1):217-230.
Housman S, Mcwhorter P, Barie P, Nicolau D. Ertapenem concentrations in obese patients undergoing surgery. Surg Infect (Larchmt). 2022;23(6):545-549.
Chen M, Nafziger AN, Drusano GL, Ma L, Bertino JS. Comparative pharmacokinetics and pharmacodynamic target attainment of ertapenem in normal-weight, obese, and extremely obese adults. Antimicrob Agents Chemother. 2006;50(4):1222-1227.
Borracci T, Adembri C, Accetta G, et al. Use of the parenteral antibiotic ertapenem As short term prophylaxis in bariatric surgery: a Pharmaco-kinetic-pharmacodynamic study in class III obese female patients. Minerva Anestesiol. 2014;80(9):1005-1011.
Chambers J, Page-Sharp M, Salman S, et al. Ertapenem for osteoarticular infections in obese patients: a pharmacokinetic study of plasma and bone concentrations. Eur J Clin Pharmacol. 2019;75(4):511-517.
Chung EK, Cheatham SC, Fleming MR, Healy DP, Kays MB. Population pharmacokinetics and pharmacodynamics of meropenem in nonobese, obese, and morbidly obese patients. J Clin Pharmacol. 2017;57(3):356-368.
Alobaid AS, Wallis SC, Jarrett P, et al. Effect of obesity on the population pharmacokinetics of meropenem in critically ill patients. Antimicrob Agents Chemother. 2016;60(8):4577-4584.
Suchánková H, Strojil J. Imipenem dosing in the obese and in patients with augmented renal clearance: a PK/PD analysis. Clin Ther. 2017;39(8):E96-E97.
Impact of Obesity on the Pharmacokinetics Of Imipenem-Relebactam in ICU Patients - Tabular View - Clinicaltrials.Gov [Internet]. [Cited 2022 Dec 6]. https://clinicaltrials.gov/ct2/show/record/nct05146154
Van Rhee KP, Smit C, Wasmann RE, et al. Ciprofloxacin pharmacokinetics after Oral and intravenous administration in (morbidly) obese and non-obese individuals: a prospective clinical study. Clin Pharmacokinet. 2022 Aug;61(8):1167-1175.
Cook AM, Martin C, Adams VR, Morehead RS. Pharmacokinetics of intravenous levofloxacin administered At 750 milligrams in obese adults. Antimicrob Agents Chemother. 2011;55(7):3240-3243.
Pai MP, Cojutti P, Pea F. Levofloxacin dosing regimen in severely morbidly obese patients (BMI ≥40 kg/M(2)) should Be guided by creatinine clearance estimates based on ideal body weight and optimized by therapeutic drug monitoring. Clin Pharmacokinet. 2014;53(8):753-762.
Kurtti A, Fritz K, Elofson-Disney K, Benefield R. Obesity is not strongly associated with increased risk for febrile neutropenia during levofloxacin prophylaxis in patients with hematological malignancies receiving intermediate-risk myelosuppressive chemotherapy. J Oncol Pharm Pract. 2020;26(6):1301-1305.
Janmahasatian S, Duffull SB, Ash S, Ward LC, Byrne NM, Green B. Quantification of lean bodyweight. Clin Pharmacokinet. 2005;44(10):1051-1065.
Pai MP, Wilcox M, Chitra S, Mcgovern P. Safety and efficacy of Omadacycline by body mass index in patients with community-acquired bacterial pneumonia: subanalysis from a randomized controlled trial. Respir Med. 2021;184:106442.
Kingsley J, Mehra P, Lawrence LE, et al. A randomized, double-blind, phase 2 study to evaluate subjective and objective outcomes in patients with acute bacterial skin and skin structure infections treated with delafloxacin, linezolid or vancomycin. J Antimicrob Chemother. 2016;71(3):821-829.
Pullman J, Gardovskis J, Farley B, et al. Efficacy and safety of delafloxacin compared with vancomycin plus aztreonam for acute bacterial skin and skin structure infections: a phase 3, double-blind, Randomized Study. J Antimicrob Chemother. 2017;72(12):3471-3480.
O'Riordan W, Mcmanus A, Teras J, et al. A comparison of the efficacy and safety of intravenous followed by oral delafloxacin with vancomycin plus aztreonam for the treatment of acute bacterial skin and skin structure infections: a phase 3, multinational, double-blind, randomized study. Clin Infect Dis. 2018;67(5):657-666.
Begg EJ, Barclay ML, Duffull SB. A suggested approach to once-daily aminoglycoside dosing. Br J Clin Pharmacol. 1995;39(6):605-609.
Schwartz SN, Pazin GJ, Lyon JA, Ho M, Pasculle AW. A controlled investigation of the pharmacokinetics of gentamicin and tobramycin in obese subjects. J Infect Dis. 1978;138(4):499-505.
Blouin RA, Mann HJ, Griffen WO Jr, Bauer LA, Record KE. Tobramycin pharmacokinetics in morbidly obese patients. Clin Pharmacol Therapeut. 1979;26(4):508-512.
Bauer LA, Edwards WAD, Dellinger EP, Simonowitz DA. Influence of weight on aminoglycoside pharmacokinetics in normal weight and morbidly obese patients. Eur J Clin Pharmacol. 1983;24(5):643-647.
Sketris I, Lesar T, Zaske DE, Cipolle RJ. Effect of obesity on gentamicin pharmacokinetics. J Clin Pharmacol. 1981;21(7):288-293.
Pai MP, Nafziger AN, Bertino JS. Simplified estimation of aminoglycoside pharmacokinetics in underweight and obese adult patients. Antimicrob Agents Chemother. 2011;55(9):4006-4011.
Crass R, Ross B, Derstine B, et al. Measurement of skeletal muscle area improves estimation of aminoglycoside clearance across body size. Antimicrob Agents Chemother. 2018;62(6):e00441-18. doi: 10.1128/AAC.00441-18
Smit C, Wasmann RE, Goulooze SC, et al. A prospective clinical study characterizing the influence of morbid obesity on the pharmacokinetics of gentamicin: towards individualized dosing in obese patients. Clin Pharmacokinet. 2019;58(10):1333-1343.
Smit C, Van Schip AM, Van Dongen EPA, Brüggemann RJM, Becker ML, Knibbe CAJ. Dose recommendations for gentamicin in the real-world obese population with varying body weight and renal (Dys)function. J Antimicrob Chemother. 2020;75(11):3286-3292.
Smit C, Wasmann RE, Wiezer MJ, et al. Tobramycin clearance is best described by renal function estimates in obese and non-obese individuals: results of a prospective rich sampling pharmacokinetic study. Pharm Res. 2019;36(8):112.
Rybak MJ, Le J, Lodise TP, et al. Therapeutic monitoring of vancomycin for serious methicillin-resistant staphylococcus aureus infections: a revised consensus guideline and review by the American society of health-system pharmacists, the infectious diseases society of America, the Pediatric Infectious Diseases Society, and the society of infectious diseases pharmacists. Am J Health Syst Pharm. 2020;77(11):835-864.
Dunn RD, Crass RL, Hong J, Pai MP, Krop LC. Vancomycin volume of distribution estimation in adults with class III obesity. Am J Health Syst Pharm. 2019;76(24):2013-2018.
Denetclaw TH, Yu MK, Moua M, Dowling TC, Steinke D. Performance of a divided-load intravenous vancomycin dosing strategy for obese patients. Ann Pharmacother. 2015;49(8):861-868.
Brown ML, Hutchison AM, Mcatee AM, Gaillard PR, Childress DT. Allometric versus consensus guideline dosing in achieving target vancomycin trough concentrations. Am J Health Syst Pharm. 2017;74(14):1067-1075.
Kubiak DW, Alquwaizani M, Sansonetti D, Barra ME, Calderwood MS. An evaluation of systemic vancomycin dosing in obese patients. Open forum. Infect Dis. 2015;2(4):Ofv176.
Morrill HJ, Caffrey AR, Noh E, Laplante KL. Vancomycin dosing considerations in a real-world cohort of obese and extremely obese patients. Pharmacotherapy. 2015;35(9):869-875.
Adane ED, Herald M, Koura F. Pharmacokinetics of vancomycin in extremely obese patients with suspected or confirmed Staphylococcus Aureus infections. Pharmacotherapy. 2015;35(2):127-139.
Smit C, Wasmann RE, Goulooze SC, et al. Population pharmacokinetics of vancomycin in obesity: finding the optimal dose for (morbidly) obese individuals. Br J Clin Pharmacol. 2020;86(2):303-317.
Wright L, Childress DT, Brown ML, Wilkerson W, Maldonado R, Durham SH. Which “weigh” to go? Alternative vancomycin dosing strategies in obese patients. J Pharm Pract. 2022;31:8971900221087122.
Huang J, Wang X, Hao C, et al. Cystatin C and/or creatinine-based estimated glomerular filtration rate for prediction of vancomycin clearance in long-stay critically ill patients with persistent inflammation, immunosuppression and catabolism syndrome (PICS): a population pharmacokinetics analysis. Intern Emerg Med. 2021;16(7):1883-1893.
Teaford H, Stevens R, Rule A, et al. Prediction of vancomycin levels using cystatin C in overweight and obese patients: a retrospective cohort study of hospitalized patients. Antimicrob Agents Chemother. 2021;65(1):e01487-20. doi: 10.1128/AAC.01487-20
Assadoon MS, Pearson JC, Kubiak DW, Kovacevic MP, Dionne BW. Evaluation of vancomycin accumulation in patients with obesity. Open Forum Infect Dis. 2022;9(10):Ofac491.
Pai MP, Hong J, Krop L. Peak measurement for vancomycin AUC estimation in obese adults improves precision and lowers bias. Antimicrob Agents Chemother. 2017;61(4):02490-16. doi: 10.1128/AAC.02490-16
Ehmann L, Simon P, Busse D, et al. Risk of target non-attainment in obese compared to non-obese patients in calculated linezolid therapy. Clin Microbiol Infect. 2020;26(9):1222-1228.
Simon P, Busse D, Petroff D, et al. Linezolid concentrations in plasma and subcutaneous tissue are reduced in obese patients, resulting in a higher risk of Underdosing in critically ill patients: a controlled clinical pharmacokinetic study. J Clin Med. 2020;9(4):E1067.
Cojutti P, Pai M, Pea F. Population pharmacokinetics and dosing considerations for the use of linezolid in overweight and obese adult patients. Clin Pharmacokinet. 2018;57(8):989-1000.
Blackman A, Jarugula P, Nicolau D, et al. Evaluation of linezolid pharmacokinetics in critically ill obese patients with severe skin and soft tissue infections. Antimicrob Agents Chemother. 2021;65(2):e01619-20. doi: 10.1128/AAC.01619-20
Xie F, Mantzarlis K, Malliotakis P, et al. Pharmacokinetic evaluation of linezolid administered intravenously in obese patients with pneumonia. J Antimicrob Chemother. 2019;74(3):667-674.
Selvaskandan H, Modha DE, Denton-Beaumont R, Ashton C, Hamilton RA. High-dose oral linezolid achieved rapid clinical and microbiological recovery in a severely overweight male with long-standing infected ulcers. J Antimicrob Chemother. 2019;74(6):1755-1757.
Puzniak LA, Morrow LE, Huang DB, Barreto JN. Impact of weight on treatment efficacy and safety in complicated skin and skin structure infections and nosocomial pneumonia caused by methicillin-resistant Staphylococcus aureus. Clin Ther. 2013;35(10):1557-1570.
Rao GG, Konicki R, Cattaneo D, et al. Therapeutic drug monitoring can improve linezolid dosing regimens in current clinical practice: a review of linezolid pharmacokinetics and pharmacodynamics. Ther Drug Monit. 2020;42(1):83-92.
Dai Y, Jiang S, Chen X, et al. Analysis of the risk factors of linezolid-related Haematological toxicity in Chinese patients. J Clin Pharm Ther. 2021;46(3):807-813.
Wasserman S, Brust JCM, Abdelwahab MT, et al. Linezolid toxicity in patients with drug-resistant tuberculosis: a prospective cohort study. J Antimicrob Chemother. 2022;77(4):1146-1154.
Jaspard M, Butel N, El Helali N, et al. Linezolid-associated neurologic adverse events In patients with multidrug-resistant tuberculosis, France. Emerg Infect Dis. 2020;26(8):1792-1800.
Eimer J, Fréchet-Jachym M, Le Dû D, et al. Increased linezolid plasma concentrations are associated with the development of severe toxicity in MDR-TB treatment. Clin Infect Dis. 2022:Ciac485. doi:10.1093/cid/ciac485. Epub ahead of print.
Flanagan S, Minassian S, Passarell J, Fiedler-Kelly J, Prokocimer P. Pharmacokinetics of tedizolid in obese and nonobese subjects. J Clin Pharmacol. 2017;57(10):1290-1294.
Grégoire M, Libois JB, Waast D, et al. Pharmacokinetics of tedizolid in an obese patient after bariatric surgery. Antimicrob Agents Chemother. 2018;62(4):E02432-17.
Butterfield-Cowper J, Lodise T, Pai M. A fixed versus weight-based dosing strategy of daptomycin may improve safety in obese adults. Pharmacotherapy. 2018;38(9):981-985.
Lorenzo MP, Housman EL, Housman ST. Evaluation of fixed-dose daptomycin in obese patients with bloodstream infections caused by Staphylococcus aureus. Ann Pharmacother. 2020;54(3):290-291.
Ng JK, Schulz LT, Rose WE, et al. Daptomycin dosing based on ideal body weight versus actual body weight: comparison of clinical outcomes. Antimicrob Agents Chemother. 2014;58(1):88-93.
Shemanski S, Bennett N, Boyd S, Woods M, Ploetz J, Kennedy K. 698: evaluation of clinical effectiveness utilizing adjusted body weight for daptomycin dosing. Crit Care Med. 2016;44(12):251.
Fox AN, Smith WJ, Kupiec KE, et al. Daptomycin dosing in obese patients: analysis of the use of adjusted body weight versus actual body weight. Therapeut Adv Infect. 2019;6:2049936118820230.
Cojutti P, Carnelutti A, Mattelig S, Sartor A, Pea F. Real-time therapeutic drug monitoring-based pharmacokinetic/pharmacodynamic optimization of complex antimicrobial therapy in a critically ill morbidly obese patient. Grand round/a case study. Ther Drug Monit. 2020;42(3):349-352.
Ritchie H, Aggarwal A, Schimmel J, Lorenzo MP. Clinical failure of dalbavancin for MRSA bacteremia in patient with severe obesity and history of IVDU. J Infect Chemother. 2022;28(3):465-468.
Redell M, Sierra-Hoffman M, Assi M, et al. The CHROME study, a real-world experience of single- and multiple-dose Oritavancin for treatment of gram-positive infections. Open Forum Infect Dis. 2019;6(11):Ofz479.
Bunnell K, Pai M, Sikka M, et al. Pharmacokinetics of telavancin at fixed doses in normal-body-weight and obese (classes I, II, and III) adult subjects. Antimicrob Agents Chemother. 2018;62(4):e02475-17. doi:10.1128/AAC.02475-17
Slover CM, Nkechi A, Barriere SL, Lu Q. Telavancin for treatment of complicated skin and skin structure infections in obese patients. Fifty-First Interscience Conference on Antimicrobial agents and Chemotherapy, Chicago, IL, Abstract L1-1491 American Society For Microbiology, Washington, DC, USA. 2011.
Wu W, Ke M, Ye L, Lin C. Application of physiologically based pharmacokinetic modeling to predict the pharmacokinetics of telavancin in obesity with renal impairment. Eur J Clin Pharmacol. 2021;77(7):989-998.
Ibrahim MM, Abuelmatty AM, Mohamed GH, et al. Best tigecycline dosing for treatment of infections caused by multidrug-resistant pathogens in critically ill patients with different body weights. Drug des Devel Ther. 2018;12:4171-4179.
Tamma P, Aitken SL, Bonomo RA, Clancy CJ. IDSA Guidance on The Treatment of Antimicrobial-Resistant Gram-Negative Infections: Version 2.0 [Internet]. 2022 [Cited 2022 Oct 28]. https://Www.Idsociety.Org/Practice-Guideline/Amr-Guidance-2.0/
Pai MP, Wilcox MH, Chitra S, Mcgovern PC. Safety and efficacy of Omadacycline by BMI categories and diabetes history in two phase III randomized studies of patients with acute bacterial skin and skin structure infections. J Antimicrob Chemother. 2021;76(5):1315-1322.
Opal S, File TM Jr, Van Der Poll T, Tzanis E, Chitra S, Mcgovern PC. An integrated safety summary of Omadacycline, a novel Aminomethylcycline antibiotic. Clin Infect Dis. 2019;69(Supplement_1):S40-S47.
Asempa TE, Izmailyan S, Lawrence K, Nicolau DP. Efficacy and safety of Eravacycline in obese patients: a post hoc analysis of pooled data from the IGNITE1 and IGNITE4 clinical trials. Open Forum Infect Dis. 2020;7(12):Ofaa548.
Lam SW, Athans V. Clinical and microbiological outcomes in obese patients receiving colistin for carbapenem-resistant gram-negative bloodstream infection. Antimicrob Agents Chemother. 2019;63(9):E00531-19.
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). Pharmacotherapy. 2019;39(1):10-39.
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.
Wang P, Zhang Q, Feng M, Sun T, Yang J, Zhang X. Population pharmacokinetics of polymyxin B in obese patients for resistant gram-negative infections. Front Pharmacol. 2021;12:754844. doi:10.3389/fphar.2021.754844
Pai MP, Polymyxin B. Dosing in obese and underweight adults. Clin Infect Dis. 2013;57(12):1785.
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. 2013;57(4):524-531.
Xie YL, Liu JJ, Peng JF, et al. The pharmacokinetic challenge of polymyxin B in critically ill patients with morbid obesity. J Glob Antimicrob Resist. 2021;27:172-174.
Miglis C, Rhodes NJ, Avedissian SN, et al. Population pharmacokinetics of polymyxin B in acutely ill adult patients. Antimicrob Agents Chemother. 2018;62(3):E01475-E01417.

Auteurs

Lina Meng (L)

Department of Quality, Stanford Health Care, Stanford, California, USA.
Division of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, California, USA.
Stanford Antimicrobial Safety and Sustainability Program, Stanford, California, USA.

Emily Mui (E)

Department of Quality, Stanford Health Care, Stanford, California, USA.
Division of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, California, USA.
Stanford Antimicrobial Safety and Sustainability Program, Stanford, California, USA.

David R Ha (DR)

Department of Quality, Stanford Health Care, Stanford, California, USA.
Division of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, California, USA.
Stanford Antimicrobial Safety and Sustainability Program, Stanford, California, USA.

Christopher Stave (C)

Lane Medical Library, Stanford University School of Medicine, Stanford, California, USA.

Stan C Deresinski (SC)

Department of Quality, Stanford Health Care, Stanford, California, USA.
Division of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, California, USA.
Stanford Antimicrobial Safety and Sustainability Program, Stanford, California, USA.

Marisa Holubar (M)

Department of Quality, Stanford Health Care, Stanford, California, USA.
Division of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, California, USA.
Stanford Antimicrobial Safety and Sustainability Program, Stanford, California, USA.

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