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Ventilator-associated respiratory infection in a resource-restricted setting: impact and etiology.
Phu, Vu Dinh; Nadjm, Behzad; Duy, Nguyen Hoang Anh; Co, Dao Xuan; Mai, Nguyen Thi Hoang; Trinh, Dao Tuyet; Campbell, James; Khiem, Dong Phu; Quang, Tran Ngoc; Loan, Huynh Thi; Binh, Ha Son; Dinh, Quynh-Dao; Thuy, Duong Bich; Lan, Huong Nguyen Phu; Ha, Nguyen Hong; Bonell, Ana; Larsson, Mattias; Hoan, Hoang Minh; Tuan, Dang Quoc; Hanberger, Hakan; Minh, Hoang Nguyen Van; Yen, Lam Minh; Van Hao, Nguyen; Binh, Nguyen Gia; Chau, Nguyen Van Vinh; Van Kinh, Nguyen; Thwaites, Guy E; Wertheim, Heiman F; van Doorn, H Rogier; Thwaites, C Louise.
Affiliation
  • Phu VD; National Hospital for Tropical Diseases, Hanoi, Vietnam.
  • Nadjm B; Oxford University Clinical Research Unit, Hanoi, Vietnam.
  • Duy NHA; Oxford University Clinical Research Unit, Hanoi, Vietnam.
  • Co DX; Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, UK.
  • Mai NTH; Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
  • Trinh DT; Bach Mai Hospital, Hanoi, Vietnam.
  • Campbell J; Oxford University Clinical Research Unit, Hanoi, Vietnam.
  • Khiem DP; Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
  • Quang TN; Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
  • Loan HT; National Hospital for Tropical Diseases, Hanoi, Vietnam.
  • Binh HS; Oxford University Clinical Research Unit, Hanoi, Vietnam.
  • Dinh QD; Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, UK.
  • Thuy DB; Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
  • Lan HNP; National Hospital for Tropical Diseases, Hanoi, Vietnam.
  • Ha NH; National Hospital for Tropical Diseases, Hanoi, Vietnam.
  • Bonell A; Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
  • Larsson M; Bach Mai Hospital, Hanoi, Vietnam.
  • Hoan HM; Oxford University Clinical Research Unit, Hanoi, Vietnam.
  • Tuan DQ; Oxford University Clinical Research Unit, Hanoi, Vietnam.
  • Hanberger H; Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
  • Minh HNV; Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
  • Yen LM; Oxford University Clinical Research Unit, Hanoi, Vietnam.
  • Van Hao N; Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
  • Binh NG; Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
  • Chau NVV; National Hospital for Tropical Diseases, Hanoi, Vietnam.
  • Van Kinh N; Oxford University Clinical Research Unit, Hanoi, Vietnam.
  • Thwaites GE; Karolinska Institutet, Stockholm, Sweden.
  • Wertheim HF; Bach Mai Hospital, Hanoi, Vietnam.
  • van Doorn HR; Bach Mai Hospital, Hanoi, Vietnam.
  • Thwaites CL; Linköping University, Linköping, Sweden.
J Intensive Care ; 5: 69, 2017.
Article in En | MEDLINE | ID: mdl-29276607
ABSTRACT

BACKGROUND:

Ventilator-associated respiratory infection (VARI) is a significant problem in resource-restricted intensive care units (ICUs), but differences in casemix and etiology means VARI in resource-restricted ICUs may be different from that found in resource-rich units. Data from these settings are vital to plan preventative interventions and assess their cost-effectiveness, but few are available.

METHODS:

We conducted a prospective observational study in four Vietnamese ICUs to assess the incidence and impact of VARI. Patients ≥ 16 years old and expected to be mechanically ventilated > 48 h were enrolled in the study and followed daily for 28 days following ICU admission.

RESULTS:

Four hundred fifty eligible patients were enrolled over 24 months, and after exclusions, 374 patients' data were analyzed. A total of 92/374 cases of VARI (21.7/1000 ventilator days) were diagnosed; 37 (9.9%) of these met ventilator-associated pneumonia (VAP) criteria (8.7/1000 ventilator days). Patients with any VARI, VAP, or VARI without VAP experienced increased hospital and ICU stay, ICU cost, and antibiotic use (p < 0.01 for all). This was also true for all VARI (p < 0.01 for all) with/without tetanus. There was no increased risk of in-hospital death in patients with VARI compared to those without (VAP HR 1.58, 95% CI 0.75-3.33, p = 0.23; VARI without VAP HR 0.40, 95% CI 0.14-1.17, p = 0.09). In patients with positive endotracheal aspirate cultures, most VARI was caused by Gram-negative organisms; the most frequent were Acinetobacter baumannii (32/73, 43.8%) Klebsiella pneumoniae (26/73, 35.6%), and Pseudomonas aeruginosa (24/73, 32.9%). 40/68 (58.8%) patients with positive cultures for these had carbapenem-resistant isolates. Patients with carbapenem-resistant VARI had significantly greater ICU costs than patients with carbapenem-susceptible isolates (6053 USD (IQR 3806-7824) vs 3131 USD (IQR 2108-7551), p = 0.04) and after correction for adequacy of initial antibiotics and APACHE II score, showed a trend towards increased risk of in-hospital death (HR 2.82, 95% CI 0.75-6.75, p = 0.15).

CONCLUSIONS:

VARI in a resource-restricted setting has limited impact on mortality, but shows significant association with increased patient costs, length of stay, and antibiotic use, particularly when caused by carbapenem-resistant bacteria. Evidence-based interventions to reduce VARI in these settings are urgently needed.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Observational_studies / Risk_factors_studies Language: En Journal: J Intensive Care Year: 2017 Document type: Article Affiliation country: Vietnam

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Observational_studies / Risk_factors_studies Language: En Journal: J Intensive Care Year: 2017 Document type: Article Affiliation country: Vietnam
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