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The Susceptibility of MDR-K. Pneumoniae to Polymyxin B Plus its Nebulised Form Versus Polymyxin B Alone in Critically Ill South Asian Patients Cover

The Susceptibility of MDR-K. Pneumoniae to Polymyxin B Plus its Nebulised Form Versus Polymyxin B Alone in Critically Ill South Asian Patients

Open Access
|Jan 2021

Figures & Tables

Table 1

Demographic and baseline characteristics of the patients

Variables
PIVNL group (n=64)PIV group (n=57)
Age (year)
Mean64.1±16.163.9±14.3
Range (min-max)20-8620-870.950
Gender
Male3733
Female27240.993
Comorbidities
Hypertension, n (%)31 (48.4)26 (45.6)0.756
Diabetes mellitus, n (%)30 (46.8)27 (47.3)0.957
Chronic lung diseases, n (%)16 (25)13 (22.8)0.778
APACHE II Score (0-30)
Mean18±4.818.3±5.5
Range (min-max)10–308–300.727
C-reactive protein (<10.0 mg/mL)
Mean161.7(112.8)139.2±105.3
Range (min-max)11.7–393.610.3–390.30.260
Procalcitonin (<0.1 ng/mL)
Mean7.5(17.3)7.4±14.4
Range (min-max)0.2–1140.1–68.50.976
White blood cell (4-11 K/μL)
Mean19.2(7.3)18.9±7.3
Range (min-max)9.7–46.111.1–47.60.823
Serum creatinine (0.8-1.4 mg/dL)
Mean1.6(0.5)1.5±0.5
Range (min-max)0.6–2.30.6–2.50.905
Table 2

Extubation, reintubation and hospitalisation time of the patients

GroupTime to extubation, n (%)p-valueICU length-of-stay, n (%)p-value21-day reintubation, n (%)P value
≥4 weeks: nil≥4 weeks: 4 (6.25)
PIVNL≥3 weeks: 1 (1.5)≥3 weeks: 7 (10.9)
(n=64)≥2 weeks: 19 (29.7)≥2 weeks: 38 (59.4)8 (12.5)
≥1 week: 40 (62.5)≥1 week: 14 (21.9)
<1 week: 4 (6.3)<1 week: 1 (1.6)
≥4 weeks: 13 (22.8)0.001**≥1 weeks: 36 (63.2)0.002**0.089**
≥3 weeks: 15 (26.3)≥3 weeks: 14 (24.5)
PIV≥2 weeks: 25 (43.9)≥2 weeks: 4 (7.0)17 (29.8)
(n=57)≥1 week: 4 (7.0)≥1 week: nil
<1 week: nil<1 week: 3 (5.3)
Table 3

Clinical outcomes of patients with intravenous polymyxin B with or without the nebulised form.

ParameterOdds ratio (95% confidence interval)p-value
Microbial eradication0.19 (0.06-0.58)0.003
Secondary bacterial infection0.17 (0.05-0.59)0.005
30-day mortality0.45 (0.14-1.43)0.178
Fig. 1

Kaplan-Meier 30-day survival curve for intravenous polymyxin B with nebulization (green line) and only intravenous polymyxin B (blue line). Analysis run using Group (polymyxin B intravenously with nebulization vs intravenous polymyxin B only) as factor; death as event and time to death as time variable.

Fig. 2

Adverse events associated with polymyxin B in both the groups (polymyxin B intravenously with nebulization vs intravenous polymyxin B alone)

DOI: https://doi.org/10.2478/jccm-2020-0044 | Journal eISSN: 2393-1817 | Journal ISSN: 2393-1809
Language: English
Page range: 28 - 36
Submitted on: Jul 15, 2020
Accepted on: Nov 23, 2020
Published on: Jan 29, 2021
Published by: University of Medicine, Pharmacy, Science and Technology of Targu Mures
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2021 Md. Jahidul Hasan, Raihan Rabbani, Ahmad Mursel Anam, Ario Santini, Shihan Mahmud Redwanul Huq, published by University of Medicine, Pharmacy, Science and Technology of Targu Mures
This work is licensed under the Creative Commons Attribution 4.0 License.