Table 2.
Reference | Country | N Subjectsa | N Samplesb | Treatmentc | Lengthd |
---|---|---|---|---|---|
(De La Cochetière et al. 2005) | Francee | 6 [0] | 1; 1–4; 2 | AMX, 3×500 mg [5 days] | 55 |
(Jernberg et al. 2007) | Swedene | 4 [4] | 1; 1; 7 | CLI, 4×150 mg [7 days] | ∼730 |
(Dethlefsen et al. 2008) | USAe | 3 [0] | 2-4; 1–2; 2 | CIP, 2×500 mg [5 days] | 175 |
(Jakobsson et al. 2010) | Swedene | 3 [3] | 1; 1; 2 | MTR, 2×400 mg; CIP, 2×250 mg; OME, 2×20 mg [7 days] | ∼1460 |
(Dethlefsen and Relman 2011) | USA | 3 [0] | 11; 5; 20–24; 4–5; 10–12f | CIP, 2×500 mg [5 days] | 37-103 |
(Morotomi et al. 2011) | Japan | 5 [29] | 0-1; 0–1; 0–2 | Various, 150–3000 mg [1-8 days] | 0-20 |
(Bajaj et al. 2013) | USA | 20 [0] | 1; 1; 0 | RFX, 2×550 mg [∼56 days] | 0 |
(O'Sullivan et al. 2013) | Ireland | 42 [143]g | 1g | Various, Not Specified | ≤31 |
(Pérez-Cobas et al. 2013b) | Germany | 1 [0] | 1; 4; 1 | SAM + CFZ, Not Specified [14 days] | 26 |
(Arat et al. 2015) | USAe | 46 [15] | 1; 1; 0 | GSK, 500–3000 mg [1-4 days] | 0 |
(Ladirat et al. 2014) | Netherlands | 10 [0] | 2; 2; 0–4 | AMX, 3×375 mg [5 days] | 21 |
(Panda et al. 2014) | Spaine | 21 [0] | 1; 1; 0 | Various, Not Specified [7 days] | 0 |
(Abeles et al. 2015) | USAe | 4 [5] | 0; 3; 0 | Various, Not Specified [≥42 days] | 0 |
(Heinsen et al. 2015) | Germanye | 5 [0] | 1; 1; 1 | PMM, 4000 mg [3 days] | 43 |
(Rashid et al. 2015) | Swedene | 19 [10] | 1; 1; 3–4 | CIP, 2×500 mg; CLI 4×150 mg [10 days] | ∼356 |
(Stewardson et al. 2015) | Switzerland | 22 [20] | 1; 1; 1 | Various, Various [Not Specified] | ∼28 |
(Willmann et al. 2015) | Germany | 2 [0] | 1; 3; 2 | CIP, 2×500 mg [6 days] | 28 |
(Zaura et al. 2015) | UK and Sweden | 43 [23] | 1; 1; 4 | Various, Various [5-10 days]] | ∼356 |
(Raymond et al. 2016) | Canada | 18 [6] | 1; 1; 1 | CPR, 2×500 mg [7 days] | 90 |
(Wipperman et al. 2017) | Haiti | 38 [101]g | 1g | HRZE, Not Specified [≥∼183 days] | 34-1202 |
(MacPherson et al. 2018) | Canadae | 70 [0] | 1; 1; 2 | AMX, 875 mg; CLA 125 mg [7 days] | ∼14 |
(Suez et al. 2018) | Israele | 21 [25] | 7; 7; 14 | CIP, 2×500 mg; MTR, 3×500 mg [7 days] | 180 |
(Dubinsky et al. 2020) | Israel | 33 [16] | 75 / 159h | Various, Various, [14-4646 days] | Various |
‘N subjects’ column shows the number of treated subjects covered by the study, followed by the number of untreated controls in square brackets.
‘N samples’ column shows the number of samples taken from each subject, with samples taken before, during and after treatment separated by semicolons.
‘Treatment’ column shows the antibiotic treatment administered to the subjects, listing first the drug, then the daily dose, then the length of the course in square brackets. Drug codes used are: AMX/Amoxicillin, CLI/Clindamycin, CIP/Ciprofloxacin, MTR/Metronidazole, OME/Omeprazole, RFX/Rifaximin, SAM/Ampicillin-Sulbactam, CFZ/Cefazolin, GSK/GSK1322322, PMM/Paromomycin, CPR/Cefprozil, HRZE/Isoniazid-Rifampin-Pyrazinamide-Ethambutol, CLA/Clavulanic Acid.
‘Length’ column shows the length of the study, shown as the number of days between the end of treatment and the last sample collected.
Location inferred from author locations and locations of ethical approval.
Study encompassed two courses of antibiotic treatment, and samples are listed in the format: before treatment; during first treatment; interval; during second treatment; after treatment.
Study used cross-sectional experimental design, so each subject was only sampled once.
Study collected a widely different number of samples from each subject, for a total of 75 antibiotic associated and 159 non-associated samples.