| Literature DB >> 26002183 |
Abstract
The casualties of global conflict attract media attention and sympathy in public, governmental, and non-governmental circles. Hospitals in developed countries offering specialist reconstructive or tertiary services are not infrequently asked to accept civilian patients from overseas conflict for complex surgical procedures or rehabilitation. Concern about the infection prevention and control risks posed by these patients, and the lack of a good evidence base on which to base measured precautions, means that the precautionary principle of accepting zero risk is usually followed. The aim of this article is to highlight infection control considerations that may be required when treating casualties from overseas conflict, based partly on our own experience. Currently there is a lack of published evidence and national consensus on how to manage these patients. The precautionary principle requires that there is an ongoing search for evidence and knowledge that can be used to move towards more traditional risk management. We propose that only by gathering the experiences of the many individual hospitals that have each cared for small numbers of such patients can such evidence and knowledge be assimilated.Entities:
Keywords: Casualties; Civilian; Infection control assessment; Precautionary principle; Risk management; War
Mesh:
Year: 2015 PMID: 26002183 PMCID: PMC7134502 DOI: 10.1016/j.jhin.2015.03.011
Source DB: PubMed Journal: J Hosp Infect ISSN: 0195-6701 Impact factor: 3.926
Bacterial infections to consider in patients transferred from conflict areas overseas
| Bacteria | Suggested screening sites | Suggested screening regimen |
|---|---|---|
| Multidrug-resistant, extensively drug-resistant and pandrug-resistant Gram-negative bacteria | Rectal swabs or faeces; respiratory secretions or throat swabs; wound swabs; urine | Three stool specimens or rectal swabs taken on separate days. Samples plated on to commercial chromogenic agar or tested by nucleic acid amplification. |
| MRSA | Nose, throat and groin/perineum swabs; wound swabs; swabs of indwelling device exit sites | On admission |
| Glycopeptide-resistant enterococci | Rectal swabs or faeces | Three stool specimens or rectal swabs taken on separate days. Samples plated on to commercial chromogenic agar or tested by nucleic acid amplification. |
| Enteric pathogens: | Up to three faeces samples | Suggest sending one stool sample on admission, regardless of whether formed or not, to ascertain if patient is colonized with enteric pathogens. Culture via validated technique or use nucleic acid amplification. Enrichment techniques should be used to detect salmonella carriage, even if NAATs are used. |
| Symptoms of active TB should be sought on admission with a chest radiograph if appropriate. | Obtain chest radiograph on admission. If patient likely to be admitted to healthcare facility for >6 months, suggest screen for latent TB using interferon gamma-release assay. |
PVL, Panton–Valentine leucocidin; MRSA, meticillin-resistant Staphylococcus aureus; NAAT, nucleic acid amplification tests; TB, tuberculosis.
Viral infections to consider in patients transferred from conflict areas overseas
| Virus type | Suggested screening methods | Suggested screening regimen |
|---|---|---|
| Hepatitis B, C; HIV | Test serum for the presence of HBsAg, hepatitis C antibody and HIV antigen/antibody on admission (with consent). | Gain consent for testing on admission to healthcare facility |
| Measles | Consider prevalence of measles in the country of origin. Measles IgG antibody measurement may be used to assess immunity. | Suggest measure measles IgG on admission and then a week later to confirm result |
| Polioviruses | Consider whether wild-type poliovirus is circulating in country of origin. Testing of faeces may be indicated. | Consult WHO list of countries in which wild poliovirus is circulating. If patient is at risk, send three stool specimens taken on separate days for enterovirus- or poliovirus- specific nucleic acid amplification testing. |
| Viral agents of gastroenteritis | Consider testing faeces only if symptomatic | Send liquid stool or vomitus for norovirus testing as part of the investigation of outbreaks of diarrhoea and vomiting if indicated |
| Varicella-zoster virus (VZV) | VZV IgG antibody measurement may be used to assess immunity | Send clotted blood on admission for VZV IgG unless confident about past infection status |
| Respiratory viruses, particularly influenza and Middle-Eastern respiratory syndrome (MERS) coronavirus | Establish case definitions, and test symptomatic patients as required |
HIV, human immunodeficiency virus; WHO, World Health Organization.
Parasitic infections to consider in patients transferred from conflict areas overseas
| Parasite | Suggested screening methods | Suggested screening regimen |
|---|---|---|
| Up to three faeces samples | Three stool specimens taken on separate days. Samples tested by conventional staining and microscopy techniques or by validated nucleic acid amplification if available. | |
| Ectoparasites: lice and scabies | Clothes, hair, and skin should be thoroughly examined on arrival |