Hospital-Acquired Pneumonia in a Multipurpose Intensive Care Unit: One-Year Prospective Study

被引:11
|
作者
Costa, Rui Dias [1 ]
Baptista, Joao Pedro [2 ]
Freitas, Ricardo [2 ]
Martins, Paulo Jorge [2 ]
机构
[1] Ctr Hosp Tondela Viseu, Dept Internal Med, Viseu, Portugal
[2] Ctr Hosp & Univ Coimbra, Dept Intens Care, Coimbra, Portugal
来源
ACTA MEDICA PORTUGUESA | 2019年 / 32卷 / 12期
关键词
Cross Infection; Drug Resistance; Multiple; Bacterial; Healthcare-Associated Pneumonia; Intensive Care Units; Pneumonia; Ventilator-Associated; VENTILATOR-ASSOCIATED PNEUMONIA; DE-ESCALATION THERAPY; COLONIZATION PRESSURE; MORTALITY; RISK; RESISTANCE; SEPSIS; ADULTS;
D O I
10.20344/amp.11607
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Hospital-acquired pneumonia continues to be a frequent complication in the intensive care unit and an important cause of admission in the intensive care unit. The aim of our study was to evaluate the demography, incidence, risk factors, causative bacterial pathogens and outcome of all episodes of Hospital-acquired pneumonia in our unit. Material and Methods: Prospective observational study, at a tertiary university hospital during one year (2014) including all the cases of hospital-acquired pneumonia in the intensive care unit. Results: Sixty patients were identified with pneumonia. Thirty-five (58.3%) had an intensive care unit acquired pneumonia, corresponding to 6.9 cases/1000 intubation-days. Antibiotic treatment in the previous 30 days was present in 75% of the cases. The incidence of Staphylococcus aureus, Pseudomonas aeruginosa and Acinetobacter baumannii was 26.2%, 20.0% and 9.2%, respectively. Patients with late-onset hospital-acquired pneumonia (>= 7 days) showed higher frequency of non-fermenting Gram-negative bacilli isolates, and methicillin-resistant S. aureus. Combination therapy was performed in 67.0%, and de-escalation in 18.3%. The mortality rate was 18.3%. The adjusted odds ratio for intensive care unit mortality in the group of patients with non-intensive care unit acquired pneumonia was 5.2 (95% CI of 1.02 - 22.10; p = 0.046). Discussion: The knowledge of local bacterial flora and resistance patterns is of crucial importance and strongly recommended. This evidence increases the probability of success of empiric antibiotic therapy. Conclusion: S. aureus was the predominant causative agent of nosocomial pneumonia. The most frequent risk factor identified for infection with multidrug-resistant organisms was previous treatment with antibiotics. Multidrug-resistant organisms were present in 45% of documented hospital-acquired pneumonias. In admitted patients with non-intensive care unit acquired pneumonia, the intensive care unit mortality rate was nearly five times higher compared to intensive care unit acquired pneumonia.
引用
收藏
页码:746 / 753
页数:8
相关论文
共 50 条
  • [41] Risk factors for hospital-acquired pneumonia caused by imipenem-resistant Pseudomonas aeruginosa in an intensive care unit
    Furtado, G. H.
    Gales, A. C.
    Perdiz, L. B.
    Santos, A. F.
    Wey, S. B.
    Medeiros, E. A.
    [J]. ANAESTHESIA AND INTENSIVE CARE, 2010, 38 (06) : 994 - 1001
  • [42] Impact of chronic liver disease in intensive care unit acquired pneumonia: a prospective study
    Marta Di Pasquale
    Mariano Esperatti
    Ernesto Crisafulli
    Miquel Ferrer
    Gianluigi Li Bassi
    Mariano Rinaudo
    Angels Escorsell
    Javier Fernandez
    Antoni Mas
    Francesco Blasi
    Antoni Torres
    [J]. Intensive Care Medicine, 2013, 39 : 1776 - 1784
  • [43] Impact Of Chronic Liver Disease In Intensive Care Unit Acquired Pneumonia: A Prospective Study
    Di Pasquale, M.
    Ferrer, M.
    Esperatti, M.
    Crisafulli, E.
    Li Bassi, G.
    Rinaudo, M.
    Escorsell, A.
    Fernandez, J.
    Mas, A.
    Blasi, F.
    Torres, A.
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2013, 187
  • [44] An analysis of hospital-acquired bacteraemia in intensive care unit patients in a university hospital in Kuwait
    Jamal, WY
    El-Din, K
    Rotimi, VO
    Chugh, TD
    [J]. JOURNAL OF HOSPITAL INFECTION, 1999, 43 (01) : 49 - 56
  • [45] Impact of chronic liver disease in intensive care unit acquired pneumonia: a prospective study
    Di Pasquale, Marta
    Esperatti, Mariano
    Crisafulli, Ernesto
    Ferrer, Miquel
    Bassi, Gianluigi Li
    Rinaudo, Mariano
    Escorsell, Angels
    Fernandez, Javier
    Mas, Antoni
    Blasi, Francesco
    Torres, Antoni
    [J]. INTENSIVE CARE MEDICINE, 2013, 39 (10) : 1776 - 1784
  • [46] PREVALENCE OF HOSPITAL-ACQUIRED INFECTION IN INTENSIVE CARE UNIT: A HOSPITAL-BASED STUDY FROM A TERTIARY CARE HOSPITAL OF BIHAR
    Suman, Keshri K.
    Ratnesh, Kumar
    Nidhi, Prasad
    Rakesh, Kumar
    Shailesh, Kumar
    Namrata, Kumari
    Anima, Xess
    Shahi, S. K.
    [J]. JOURNAL OF EVOLUTION OF MEDICAL AND DENTAL SCIENCES-JEMDS, 2016, 5 (73): : 5381 - 5384
  • [47] Prognosis of hospital-acquired pneumonia/ventilator-associated pneumonia with Stenotrophomonas maltophilia versus Klebsiella pneumoniae in intensive care unit: A retrospective cohort study
    Chen, Shuping
    Zou, Dongdong
    [J]. CLINICAL RESPIRATORY JOURNAL, 2022, 16 (10): : 669 - 676
  • [48] Oral Care Clinical Trial to Reduce Non-Intensive Care Unit, Hospital-Acquired Pneumonia: Lessons for Future Research
    McNally, Edel
    Krisciunas, Gintas P.
    Langmore, Susan E.
    Crimlisk, Janet T.
    Pisegna, Jessica M.
    Massaro, Joseph
    [J]. JOURNAL FOR HEALTHCARE QUALITY, 2019, 41 (01) : 1 - 9
  • [49] A one-year prospective study of colonization with antimicrobial-resistant organisms on admission to a Vietnamese intensive care unit
    Duong Bich Thuy
    James Campbell
    Nguyen Van Minh Hoang
    Truong Thi Thuy Trinh
    Ha Thi Hai Duong
    Nguyen Chi Hieu
    Nguyen Hoang Anh Duy
    Nguyen Van Hao
    Stephen Baker
    Thwaites, Guy E.
    Nguyen Van Vinh Chau
    Louise Thwaites, C.
    [J]. PLOS ONE, 2017, 12 (09):
  • [50] The costs of septic syndromes in the intensive care unit and influence of hospital-acquired sepsis
    Brun-Buisson, C
    Roudot-Thoraval, F
    Girou, E
    Grenier-Sennelier, C
    Durand-Zaleski, I
    [J]. INTENSIVE CARE MEDICINE, 2003, 29 (09) : 1464 - 1471