A clinical study on the pattern of antimicrobial drug use and drug resistance in patients with ventilator-associated pneumonia in a tertiary care hospital

被引:2
作者
Rezia, Abisha [1 ]
Vijendra, R. [1 ,2 ]
机构
[1] Kempegowda Inst Med Sci, Dept Pharmacol, Bengaluru, Karnataka, India
[2] Kempegowda Inst Med Sci, Dept Pharmacol, Bengaluru 560070, Karnataka, India
关键词
Antimicrobial drug resistance; clinical pulmonary infection score; intensive care; ventilator-associated pneumonia; INFECTION-CONTROL; RISK-FACTORS; ONSET; UNITS;
D O I
10.4103/ijp.ijp_759_21
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
CONTEXT: Ventilator-associated pneumonia (VAP) develops nearly in about one-third of the patients, 48 h after receiving mechanical ventilation. Common pathogens are Pseudomonas aeruginosa, Staphylococcus aureus, Acinetobacter spp., Klebsiella spp., Escherichia coli, Proteus spp., Enterobacter spp. and Enterococcus spp. including multidrug-resistant pathogens. AIM: The study aims to assess the pattern of antimicrobial drug use in VAP and to assess the etiological organisms and their drug sensitivity and resistance pattern. SETTINGS AND DESIGN: Study participants admitted to Kempegowda Institute of Medical Sciences Hospital and Research Centre, Bengaluru, and who developed VAP were included in this prospective observational study. SUBJECTS AND METHODS: Bronchial secretions were subjected to microbiological analysis. The etiological organisms, their drug sensitivity and resistance pattern, and the outcome of drug therapy were recorded. The clinical course of the study participants was monitored till either the resolution of pneumonia or the demise of the participant. STATISTICAL ANALYSIS USED: Qualitative data were analyzed using the Chi-square test or Fischer's exact test and quantitative data using the independent t-test. RESULTS: Early VAP was seen in 91.7% and late VAP in 8.3% of the participants. The organisms isolated were S. aureus, Enterococcus spp., Acinetobacter spp., Klebsiella pneumoniae and P. aeruginosa. Majority of the study participants with early VAP (75%, n = 41) completely recovered from pneumonia and 80%, n = 4 participants with late VAP recovered completely. CONCLUSION: The organisms had a varied sensitivity and resistance pattern. The clinical outcome was multifactorial and its association with specific antimicrobial agents cannot be drawn.
引用
收藏
页码:89 / 96
页数:8
相关论文
共 21 条
[11]  
Mandell LA, 2018, HARRISONS PRINCIPLES, V20th, P908
[12]  
Mandell LA, 2018, HARRISONS PRINCIPLES, V20th, P910
[13]  
Patil Harsha V, 2017, J Nat Sci Biol Med, V8, P46, DOI [10.4103/0976-9668.198360, 10.4103/0976-9668.198360]
[14]   Comparison of the Bacterial Etiology of Early-Onset and Late-Onset Ventilator-Associated Pneumonia in Subjects Enrolled in 2 Large Clinical Studies [J].
Restrepo, Marcos I. ;
Peterson, Janet ;
Fernandez, Juan F. ;
Qin, Zhihai ;
Fisher, Alan C. ;
Nicholson, Susan C. .
RESPIRATORY CARE, 2013, 58 (07) :1220-1225
[15]   Nosocomial infections in combined medical-surgical intensive care units in the United States [J].
Richards, MJ ;
Edwards, JR ;
Culver, DH ;
Gaynes, RP .
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2000, 21 (08) :510-515
[16]  
Saravanan Revathy, 2013, J Basic Clin Pharm, V4, P56, DOI 10.4103/0976-0105.118797
[17]   Revised Kuppuswamy's Socioeconomic Status Scale: Explained and Updated [J].
Sharma, Rahul .
INDIAN PEDIATRICS, 2017, 54 (10) :867-870
[18]  
Timsit Jean-Francois, 2017, F1000Res, V6, P2061, DOI [10.12688/f1000research.12222.1, 10.12688/f1000research.12222.1]
[19]   Patterns of antimicrobial resistance in intensive care unit patients: a study in Vietnam [J].
Tran, Giang M. ;
Ho-Le, Thao P. ;
Ha, Duc T. ;
Tran-Nguyen, Chau H. ;
Nguyen, Tuyet S. M. ;
Pham, Thao T. N. ;
Nguyen, Tuyet A. ;
Nguyen, Dung A. ;
Hoang, Hoa Q. ;
Tran, Ngoc V. ;
Nguyen, Tuan V. .
BMC INFECTIOUS DISEASES, 2017, 17
[20]   Estimates of the global, regional, and national morbidity, mortality, and aetiologies of lower respiratory tract infections in 195 countries: a systematic analysis for the Global Burden of Disease Study 2015 [J].
Troeger, Christopher ;
Forouzanfar, Mohammad ;
Rao, Puja C. ;
Khalil, Ibrahim ;
Brown, Alexandria ;
Swartz, Scott ;
Fullman, Nancy ;
Mosser, Jonathan ;
Thompson, Robert L. ;
Reiner, Robert C., Jr. ;
Abajobir, Amanuel ;
Alam, Noore ;
Alemayohu, Mulubirhan Assefa ;
Amare, Azmeraw T. ;
Antonio, Carl Abelardo ;
Asayesh, Hamid ;
Avokpaho, Euripide ;
Barac, Aleksandra ;
Beshir, Muktar A. ;
Boneya, Dube Jara ;
Brauer, Michael ;
Dandona, Lalit ;
Dandona, Rakhi ;
Fitchett, Joseph R. A. ;
Gebrehiwot, Tsegaye Tewelde ;
Hailu, Gessessew Buggsa ;
Hotez, Peter J. ;
Kasaeian, Amir ;
Khoja, Tawfik ;
Kissoon, Niranjan ;
Knibbs, Luke ;
Kumar, G. Anil ;
Rai, Rajesh Kumar ;
Abd El Razek, Hassan Magdy ;
Mohammed, Muktar S. K. ;
Nielson, Katie ;
Oren, Eyal ;
Osman, Abdalla ;
Patton, George ;
Qorbani, Mostafa ;
Roba, Hirbo Shore ;
Sartorius, Benn ;
Savic, Miloje ;
Shigematsu, Mika ;
Sykes, Bryan ;
Swaminathan, Soumya ;
Topor-Madry, Roman ;
Ukwaja, Kingsley ;
Werdecker, Andrea ;
Yonemoto, Naohiro .
LANCET INFECTIOUS DISEASES, 2017, 17 (11) :1133-1161