Jessica Barrett
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Jessica Barrett has a total of 13 co-authors. Here are the top co-authors by number of shared publications:
William Newsholme
Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, St Thomas' Hospital, Westminster Bridge Road, London SE1 7EH, UK
2 shared publications- Christopher J. M. Whitty
London School of Hygiene and Tropical Medicine, London, UK
1 shared publication - Claire Broderick
Department of infectious disease, Imperial College London, London, UK
1 shared publication - Clare E. Warrell
Hospital for Tropical Diseases, University College London Hospitals NHS Foundation Trust
1 shared publication Duncan Wyncoll
Kings Coll London, Sch Med, London SE1 7EH, England
1 shared publicationHannah Soulsby
Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, St Thomas' Hospital, Westminster Bridge Road, London SE1 7EH, UK
1 shared publication
Latest Publications
- 1 October 2017
- Published by Elsevier in Journal of Infection
- Vol. 75 (4) , 301-308
The changing aetiology of eosinophilia in migrants and returning travellers in the Hospital for Tropical Diseases, London 2002–2015: An observational study
- 1 October 2017
- Published by Elsevier in Journal of Infection
- Vol. 75 (4) , 301-308
The changing aetiology of eosinophilia in migrants and returning travellers in the Hospital for Tropical Diseases, London 2002–2015: An observational study
- 12 October 2015
- Published by Oxford University Press (OUP) in Journal of Antimicrobial Chemotherapy
- Vol. 71 (1) , 220-225
Subcutaneous ivermectin use in the treatment of severeStrongyloides stercoralisinfection: two case reports and a discussion of the literature: Table 1.
Background Strongyloides stercoralis infection presents with varying degrees of severity, but it often primarily involves the small bowel. In severe infection and cases of hyperinfection, ileus and small-bowel obstruction may prevent enteral absorption of anthelminthics such as ivermectin. At present there are no parenteral anthelminthics licensed for use in humans. Methods Here, we describe two cases of severe S. stercoralis infection treated with an unlicensed veterinary preparation of subcutaneous ivermectin, and we discuss the published reports of the use of this treatment elsewhere. Results Both patients were successfully treated with subcutaneous ivermectin, and both recovered completely. Conclusions Despite the limited published experience of parenteral ivermectin use, there is evidence that it may be a safe and effective treatment for severe strongyloidiasis. However, more data are needed to guide dosing schedules and monitoring for toxicity.
- 12 October 2015
- Published by Oxford University Press (OUP) in Journal of Antimicrobial Chemotherapy
- Vol. 71 (1) , 220-225
Subcutaneous ivermectin use in the treatment of severeStrongyloides stercoralisinfection: two case reports and a discussion of the literature: Table 1.
Background Strongyloides stercoralis infection presents with varying degrees of severity, but it often primarily involves the small bowel. In severe infection and cases of hyperinfection, ileus and small-bowel obstruction may prevent enteral absorption of anthelminthics such as ivermectin. At present there are no parenteral anthelminthics licensed for use in humans. Methods Here, we describe two cases of severe S. stercoralis infection treated with an unlicensed veterinary preparation of subcutaneous ivermectin, and we discuss the published reports of the use of this treatment elsewhere. Results Both patients were successfully treated with subcutaneous ivermectin, and both recovered completely. Conclusions Despite the limited published experience of parenteral ivermectin use, there is evidence that it may be a safe and effective treatment for severe strongyloidiasis. However, more data are needed to guide dosing schedules and monitoring for toxicity.
- 3 February 2015
- Published by Taylor & Francis in Expert Review of Anti-infective Therapy
- Vol. 13 (4) , 1-9
Shortening the course of antibiotic treatment in the intensive care unit
Effective antimicrobial stewardship is an increasingly important concern for healthcare providers globally. Antibiotics are frequently prescribed for patients who develop sepsis in the intensive care unit and traditionally courses are prolonged, with uncertain benefit and probable harm. There is little evidence to support many guidelines recommending between 10 and 14 days, and a number of studies suggest substantially shorter courses of less than 7 days may suffice. Safely reducing course length is likely to depend on a number of preconditions, including thorough eradication of any septic foci; optimization of serum antibiotic concentrations, particularly when there is physiological derangement; and use of novel biomarkers such as procalcitonin. The critical care environment is well suited to this aim as patients are closely monitored. With these measures in place, it is reasonable to believe short antibiotic courses can safely be used for the majority of intensive care infections.
- 3 February 2015
- Published by Taylor & Francis in Expert Review of Anti-infective Therapy
- Vol. 13 (4) , 1-9
Shortening the course of antibiotic treatment in the intensive care unit
Effective antimicrobial stewardship is an increasingly important concern for healthcare providers globally. Antibiotics are frequently prescribed for patients who develop sepsis in the intensive care unit and traditionally courses are prolonged, with uncertain benefit and probable harm. There is little evidence to support many guidelines recommending between 10 and 14 days, and a number of studies suggest substantially shorter courses of less than 7 days may suffice. Safely reducing course length is likely to depend on a number of preconditions, including thorough eradication of any septic foci; optimization of serum antibiotic concentrations, particularly when there is physiological derangement; and use of novel biomarkers such as procalcitonin. The critical care environment is well suited to this aim as patients are closely monitored. With these measures in place, it is reasonable to believe short antibiotic courses can safely be used for the majority of intensive care infections.