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. 2022 Mar 22;15:1205–1218. doi: 10.2147/IDR.S357746

Table 2.

Regimens, Adverse Reactions and Outcomes

Treatment Value
Preemptive therapya 207 (77.20%)
Loading dose% 110 (41.04%)
Loading dose≥2.0mg/kg 59 (22.01%)
Maintenance dose ≥1.25mg/kg q12h 39 (14.55%)
Loading dose (mg/kg) 1.01 (0.84–1.69)
Maintenance dose (mg/kg q12h) 0.85 (0.82–1.00)
Cumulative dose (mg) 928.57 (552.50–1361.11)
Treatment duration time (days) 9.67 (6.12–13.81)
Combination of drugs*
 Tigecycline 84 (31.34%)
 Carbapenems 75 (27.99%)
 β-lactams 90 (33.58%)
 Glycopeptides 44 (16.42%)
 Others 41 (15.30%)
Efficacy
 Clinical effectiveness 98/268 (36.57%)
 7-day clearance 96/326 (29.45%)
 Course of treatment clearance 136/345 (39.42%)
 Bacteria removal time (days) 6.67 (4.17–10.92)
 All-cause mortalityb 91 (33.96%)
 Survival time (days)c 10 (6.0–20.5)
Length of hospital stay (days) 36.00 (21.80–67.00)
Adverse reactions 56 (19.58%)
 Nephrotoxicity (AKI)c 22 (8.21%)
 Skin pigmentation 20 (6.99%)
 Drowsiness 4 (1.49%)
 Neuromuscular block 3 (1.12%)
 Drug-induced 2 (0.75%)
 Drug eruption 1 (0.37%)
 Itching 1 (0.37%)
 Feel nausea 1 (0.37%)
 Hepatotoxicity 1 (0.37%)
 Insomnia 1 (0.37%)

Notes: aPreemptive therapy defined as the use of PMB before or within two days of bacterial culture and drug sensitivity results; bAll-cause mortality include in-hospital deaths and patients discharged from hospital in critical condition with low blood pressure after abandonment of treatment; cSurvival time defined as the time from the beginning of PMB to the end of in-hospital death or abandonment of treatment; cNephrotoxicity (AKI): Creatinine was increased by 2 times after treatment compared with baseline (before treatment). *There were two or more drugs combined with PMB.

Abbreviations: PMB, Polymyxin B; ICU, Intensive Care Unit; APACHE II, Acute Physiology and Chronic Health Evaluation II; CR-GNB, Carbapenem-resistant Gram-negative Bacteria; MIC, minimum inhibitory concentration.