| Literature DB >> 22563403 |
Khai Tran1, Karen Cimon, Melissa Severn, Carmem L Pessoa-Silva, John Conly.
Abstract
Aerosol generating procedures (AGPs) may expose health care workers (HCWs) to pathogens causing acute respiratory infections (ARIs), but the risk of transmission of ARIs from AGPs is not fully known. We sought to determine the clinical evidence for the risk of transmission of ARIs to HCWs caring for patients undergoing AGPs compared with the risk of transmission to HCWs caring for patients not undergoing AGPs. We searched PubMed, EMBASE, MEDLINE, CINAHL, the Cochrane Library, University of York CRD databases, EuroScan, LILACS, Indian Medlars, Index Medicus for SE Asia, international health technology agencies and the Internet in all languages for articles from 01/01/1990 to 22/10/2010. Independent reviewers screened abstracts using pre-defined criteria, obtained full-text articles, selected relevant studies, and abstracted data. Disagreements were resolved by consensus. The outcome of interest was risk of ARI transmission. The quality of evidence was rated using the GRADE system. We identified 5 case-control and 5 retrospective cohort studies which evaluated transmission of SARS to HCWs. Procedures reported to present an increased risk of transmission included [n; pooled OR(95%CI)] tracheal intubation [n = 4 cohort; 6.6 (2.3, 18.9), and n = 4 case-control; 6.6 (4.1, 10.6)], non-invasive ventilation [n = 2 cohort; OR 3.1(1.4, 6.8)], tracheotomy [n = 1 case-control; 4.2 (1.5, 11.5)] and manual ventilation before intubation [n = 1 cohort; OR 2.8 (1.3, 6.4)]. Other intubation associated procedures, endotracheal aspiration, suction of body fluids, bronchoscopy, nebulizer treatment, administration of O2, high flow O2, manipulation of O2 mask or BiPAP mask, defibrillation, chest compressions, insertion of nasogastric tube, and collection of sputum were not significant. Our findings suggest that some procedures potentially capable of generating aerosols have been associated with increased risk of SARS transmission to HCWs or were a risk factor for transmission, with the most consistent association across multiple studies identified with tracheal intubation.Entities:
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Year: 2012 PMID: 22563403 PMCID: PMC3338532 DOI: 10.1371/journal.pone.0035797
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Characteristics of included studies
| Study; Country | Design/Setting | Period of evaluation | Population | Assessment of training and protective equipment? | Laboratory tests | Study quality (GRADE) |
| Raboud et al, 2010 | Retrospective cohort study; Multiple hospitals | 2003 SARS outbreak in Toronto | 624 HCWs (physicians, residents, nurses, therapists, technologists, housekeepers, others) | Yes | Culture and PCR for SARS-CoV | VERY LOW |
| Chen et al, 2009 | Case-control study; Hospital | 2003 SARS outbreak in Guangzhou | 758 HCWs (doctors, nurses, health attendants, technicians, others) | Yes | ELISA for antibody against SARS-CoV | VERY LOW |
| Liu et al, 2009 | Case-control; Hospital | 2003 SARS outbreak in Beijing | 477 HCWs (medical staff, nursing staff, others) | Yes | ELISA for antibody against SARS-CoV | VERY LOW |
| Pei et al, 2006 | Case-control study; Three hospitals | 2002–2003 SARS outbreak in Beijing and Tianjin | 443 HCWs (doctors, nurses, technicians, administrators, others) | Yes | Not mentioned of methods to detect antibodies against SARS-CoV | VERY LOW |
| Fowler et al, 2004 | Retrospective cohort study; Intensive care unit | 2003 SARS outbreak in Toronto | 122 critical care staff (physicians, nurses, nursing assistants, respiratory therapists, others) | No, on training All HCWs wore gloves, gowns, N-95/PCM 2,000 masks, and hairnets. Eye and face shields were variably employed | PCR or serology for SARS-CoV | VERY LOW |
| Loeb et al, 2004 | Retrospective cohort study; Intensive care unit; Coronary care unit | 2003 SARS outbreak in Toronto | 43 nurses | Yes | Serology, immunofluorescence | VERY LOW |
| Ma et al, 2004 | Case-control study; Five hospitals | 2003 SARS outbreak in Beijing | HCWs (nurse assistants, janitors and others) (N = 473) | Yes | Diagnostic criteria for SARS from Chinese Minister of Health | VERY LOW |
| Teleman et al, 2004 | Case-control study; Hospital | 2003 SARS outbreak in Singapore | 86 HCWs (doctors, nurses, others) | Not mentioned | Symptoms, chest X-ray and serology | VERY LOW |
| Wong et al, 2004 | Retrospective cohort study; Hospital | 2003 SARS outbreak in Hong Kong | 66 medical students | Yes, on personal protection equipmentNo, on training | Indirect immunofluorescent to detect antibodies against SARS-CoV | VERY LOW |
| Scales et al, 2003 | Retrospective cohort study; Intensive care unit | 2003 SARS outbreak in Toronto | 69 intensive care staff | Unclear | Radiographic lung infiltrates | VERY LOW |
CoV: coronavirus; HCWs: health care workers; PCR: polymerase chain reaction; SARS: severe acute respiratory syndrome.
Risk of SARS Transmission to HCWs Exposed and Not Exposed to Aerosol-Generating Procedures, and Aerosol Generating Procedures as Risk Factors for SARS Transmission
| Aerosol Generating Procedures | Odds ratio (95% CI) | |
| Point estimate | Pooled estimate; I2 | |
| Tracheal intubation (4 cohort studies) | 3.0 (1.4, 6.7) | 6.6 (2.3, 18.9); 39.6% |
| 22.8 (3.9, 131.1) | ||
| 13.8 (1.2, 161.7) | ||
| 5.5 (0.6, 49.5) | ||
| Tracheal intubation (4 case-control studies) | 0.7 (0.1, 3.9) | 6.6 (4.1, 10.6); 61.4% |
| 9.2 (4.2, 20.2) | ||
| 8.0 (3.9, 16.6) | ||
| 9.3 (2.9, 30.2) | ||
| Suction before intubation (2 cohort studies) | 13.8 (1.2, 161.7) | 3.5 (0.5, 24.6); 59.2% |
| 1.7 (0.7, 4.2) | ||
| Suction after intubation (2 cohort studies) | 0.6 (0.1, 3.0) | 1.3 (0.5, 3.4); 28.8% |
| 1.8 (0.8, 4.0) | ||
| Nebulizer treatment (3 cohort studies) | 6.6 (0.9, 50.5) | 0.9 (0.1, 13.6); 73.1% |
| 0.1 (0.0 | ||
| 1.2 (0.1, 20.7) | ||
| Manipulation of oxygen mask (2 cohort studies) | 17.0 (1.8, 165.0) | 4.6 (0.6, 32.5); 64.8% |
| 2.2 (0.9, 4.9) | ||
| Bronchoscopy (2 cohort studies) | 3.3 (0.2, 59.6) | 1.9 (0.2, 14.2); 0% |
| 1.1 (0.1, 18.5) | ||
| Non-invasive ventilation (2 cohort studies) | 2.6 (0.2, 34.5) | 3.1 (1.4, 6.8); 0% |
| 3.2 (1.4, 7.2) | ||
| Insertion of nasogastric tube (2 cohort studies) | 1.7 (0.2, 11.5) | 1.2 (0.4, 4.0); 0% |
| 1.0 (0.2, 4.5) | ||
| Chest compressions (1 case-control study) | 4.5 (1.5, 13.8) | |
| Chest compressions (2 cohort studies) | 3.0 (0.4, 24.5) | 1.4 (0.2, 11.2); 27.3% |
| 0.4 (0.0 | ||
| Defibrillation (2 cohort studies) | 0.5 (0.0 | 2.5 (0.1, 43.9); 55.3% |
| 7.9 (0.8, 79.0) | ||
| Chest physiotherapy (2 cohort studies) | 1.3 (0.2, 8.3) | 0.8 (0.2, 3.2); 0% |
| 0.5 (0.1, 3.5) | ||
| High-frequency oscillatory ventilation (1 cohort study) | 0.7 (0.1, 5.5) | |
| High flow oxygen (1 cohort study) | 0.4 (0.1, 1.7) | |
| Tracheotomy (1 case-control study) | 4.2 (1.5, 11.5) | |
| Intubation, tracheotomy, airway care, and cardiac resuscitation (1 case-control study) | 6.2 (2.2, 18.1) | |
| Manipulation of BiPAP mask (1 cohort study) | 6.2 (2.2, 18.1) | |
| Endotracheal aspiration (1 cohort study) | 1.0 (0.2, 5.2) | |
| Suction of body fluid (1 case-control study) | 1.0 (0.4, 2.8) | |
| Administration of oxygen (I case-control study) | 1.0 (0.3, 2.8) | |
| Mechanical ventilation (1 cohort study) | 0.9 (0.4, 2.0) | |
| Manual ventilation before intubation (1 cohort study) | 2.8 (1.3, 6.4) | |
| Manual ventilation after intubation (1 cohort study) | 1.3 (0.5, 3.2) | |
| Manual ventilation (1 cohort study) | 1.3 (0.2, 8.3) | |
| Collection of sputum sample (1 cohort study) | 2.7 (0.9, 8.2) | |
BiPAP: bi-level positive airway pressure; CI: confidence interval.
actual value is 0.01;
actual value is 0.02.
Figure 1Risk of SARS Transmission to HCWs Exposed to Tracheal Intubation.
Figure 2Tracheal Intubation as Risk Factor of SARS Transmission.