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. 2024 Oct 11;6(12):100913. doi: 10.1016/j.xkme.2024.100913

Table 1.

Characteristics of the Included Studies

First Author (Year), Country Study Design Comparison Daily Drug Doses (IC Group)/(Comparator Group) Study Population Total No. of Participants (IC Group/Comparator Group) Sex M:F, (IC Group)/(Comparator Group) Age, IC Group/Comparator Group, Mean (SD), y Follow-up Duration, d Outcomes Reported
Randomized controlled trials
Carmellini et al23 (1997), Italy RCT IC vs ceftazidime (500 mg/500 mg every 8 h)/(1 g every 12 h) before surgery, for 2 d Kidney transplant recipients receiving cyclosporin 69 (33/36) (15:18)/(15:11) 44.2 (9.7)/43.1 (9.8) 30 Scra and mortality
Carmellini et al24 (1998), Italy RCT IC vs ceftazidime (500 mg/500 mg every 8 h)/(2 g/d) following 2 postoperative days Kidney transplant recipients receiving cyclosporin 16 (8/8) Not specified 45 (5)/42 (4) 14 AKIb
Markewitz et al45 (1994), Germany RCT IC vs placebo control (500 mg/500 mg every 12 h) preoperatively followed by 7 d postoperatively Heart transplant patients receiving cyclosporin 20 (10/10) Not specified 51 (9.3)/5 (9.3) 10 Scrc and AKId
Schmitt et al27 (2006), Multicountry RCT IC vs piperacillin/tazobactam (1 g/1 g)/(4 g/500 mg) every 8 h for 5-21 d Hospitalized patients with nosocomial infection 217 (110/107) (64:47)/(77:33) 65.7 (13.8)/68.4 (13.7) 21 Mortality
Zanetti et al28 (2003), Multicountry RCT IC vs cefepime (2 g/2 g every 8 h)/(500 mg every 6 h) Hospitalized patients with nosocomial pneumonia 209 (101/108) (67:34)/(72:36) 53 (18)/55 (18) 14 AKIe, mortality
Observational studies
Baghai et al22 (1995), United States Observational IC vs control (500 mg/500 mg every 6 h) for 5 d Heart and lung transplant recipients receiving cyclosporin 20 (10/10) Not specified Not specified 14 Scrf
Gruss et al25 (1996), Spain Observational IC vs control Dose not reported Bone marrow transplant recipients receiving cyclosporin 104 (64/40) Not specified Not specified 30 Scrg and AKIh
Hakeam et al46 (2019), Saudi Arabia Observational IC vs meropenem 0.5 g every 6 h in 109 patients and 1 g every 8 h in 12 patients/1 g every 8 h in 98 patients and 0.5 every 8 h in 8 patients Hospitalized patients being treated for various infections with vancomycin 227 (106/121) (62:59)/(63:43) 50.7 (17.4)/50.7 (17.4) 7 Scri, AKIj, and mortality
Hornik et al29 (2014), United States Observational IC vs meropenem Dose not specified Hospitalized infants treated with carbapenem antibiotics 5566 (2087 /3256)k Not specified First 120 d of life 120 AKIl and mortality
Zaballos et al26 (2021), Spain Observational IC vs control (500 mg/500 mg every 8 h) Patients with peritoneal carcinomatosis receiving surgery and intraperitoneal cisplatin; 9.4% in the IC group versus 53.5% in the control group received cotreatment with doxorubicin 181 (83/98) (5:80)/(7:91) 56.79 (11.42)/53.22 (10.94) 7 Scrm, AKIn, and mortality

Notes: All studies included imipenem/cilastatin (IC) in the intervention group.

Abbreviations: IC, imipenem/cilastatin; M:F, male:female; RCT, randomized clinical trial; RIFLE, Risk, Injury, Failure Loss, End-stage renal disease; Scr, serum creatinine; SD, standard deviation.

oDefined by Scr measurement >1.7 mg/dL.

a

Measured on postoperative day 30.

b

Defined by Scr and urinary output changes over 14 d of follow-up.

c

Measured on postoperative days 1-10 consecutively.

d

Defined by receipt of kidney replacement therapy in the postoperative period.

e

Defined as Scr >200 μmol/L, with measurements taken at baseline, then twice weekly, and within 48 h after the completion of drug therapy and/or patient identified as a possible case of interstitial nephritis.

f

Measured on postoperative days 1-5 consecutively.

g

Measured posttransplant, days not specified.

h

Definition not specified.

i

Measured day 1 and day 4 following initiation of antibiotics.

j

Defined according to the RIFLE criteria based on changes in Scr and urinary output.

k

223 infants received both carbapenems at different times in the study.

l

Defined according to the RIFLE criteria criteria based on changes in Scr and urinary output.

m

Measured at baseline and post-intervention day 1 to day 7 consecutively.

n

Defined according to the RIFLE criteria.