scholarly journals A Case of Life-Threatening Airway Obstruction Caused by Acute Diphtheria Infection in the United Kingdom

Cureus ◽  
2021 ◽  
Author(s):  
Michael M Chu ◽  
Miriam R Bennett ◽  
Anna Harrison ◽  
Arun Cardozo
Author(s):  
Marie Wright ◽  
Sheila Javadpour ◽  
Patricia Jackson ◽  
Edile Murdoch ◽  
Felicity Mehendale ◽  
...  

2021 ◽  
pp. 105566562110005
Author(s):  
Terry-Ann Curran ◽  
Nitisha Narayan ◽  
Lynn Fenner ◽  
Guy Thornburn ◽  
Marc C. Swan ◽  
...  

Introduction: The use of throat packs during oropharyngeal surgery has long been a topic of debate among cleft surgeons. The advantage of inserting an absorbent tulle within the pharynx must be weighed against the risk of unintended retention postoperatively. Despite safety check mechanisms in place, retention may occur with potentially life-threatening consequences. We present a comprehensive review of throat pack use in all cleft units within the United Kingdom and Ireland. Methods: All 20 cleft surgery units in the United Kingdom and Ireland were surveyed on their use of throat packs in children aged 6 months to 2 years undergoing elective cleft palate surgery. Results: The response rate to the survey was 100%. Seventy-five percent of units currently use throat packs; in 40%, they are used in addition to cuffed endotracheal tubes (ETTs). Inclusion of the throat pack in the surgical swab count was perceived as the safest mechanism employed to avoid retention. 26.1% of respondents were aware of at least 1 incident of pack retention in their unit. Discussion/Conclusion: The reported UK and Irish experience demonstrates that three-quarters of units routinely use packs. Notably, a quarter of respondents to the survey have experience of an incident of throat pack retention. Nevertheless, the majority of respondents considered the perceived risk of retaining a pack to be low. The growing use of microcuffed ETTs in UK cleft units paired with a low incidence of perioperative complications when a throat pack is not introduced might prompt cleft surgeons to review routine pharyngeal packing.


Author(s):  
Omar Mostafa ◽  
Kusy Suleiman ◽  
Yusuf Abdallah

Pigmented fundus lesions on fundoscopic examination are not an uncommon finding. Pigmented tumoral lesions can arise from the retinal epithelium or choroidal melanocytes causing a spectrum of disorders, ranging from choroidal naevus and foreign bodies to the rarer choroidal melanoma. As choroidal melanoma is the most common primary malignant intraocular tumour, this educational review aims to provide a structured overview of this topic to students and junior doctors, to help establish an understanding of such a rare but life-threatening condition. This will also provide the reader with an insight on referral guidelines in the United Kingdom, a brief overview of various treatments, and factors that affect patient’s prognosis.


2017 ◽  
Vol 33 (S1) ◽  
pp. 64-65
Author(s):  
Bernarda Zamora ◽  
Martina Garau ◽  
François Maignen ◽  
Phill O'Neill ◽  
Jorge Mestre-Ferrandiz

INTRODUCTION:Under the Orphan Regulation, the European Medicines Agency (EMA) intended to incentivize the research and development of new treatments for rare and life-threatening conditions. Marketing authorisation of orphan medicinal products (OMPs) by the EMA is only the first step, as medicines are made available to patients when reimbursement or Health Technology Assessment (HTA) decisions are implemented by national health systems. We analyzed the availability and access to OMPs in the United Kingdom (UK), France, Germany, Italy and Spain. We compared the availability, which is the possibility to prescribe a given OMP, to the access, which refers to the full or partial reimbursement by the public health service.METHODS:We collected data on launches, HTA decisions, any centralized commissioning and/or reimbursement decision for all the OMPs authorised since 2000 in the UK countries (England, Scotland and Wales), France, Germany, Italy and Spain.RESULTS:Since the Orphan Regulation inception, the EMA granted marketing authorization to 143 OMPs. These OMPs are most widely accessible in Germany and France. Reimbursement in Germany is immediate after authorization. France and Italy present a delay of 19 months from authorization to reimbursement, which is shorter than in other countries. In England, less than 50 percent of centrally authorised OMPs are routinely funded by the National Health Service (NHS), including one-third of these recommended by the National Institute for Health and Care Excellence (NICE), and those reimbursed via commissioning policies and the Cancer Drugs Fund.CONCLUSIONS:The assessment of degree of access to OMPs across Europe is limited by differences in the national HTA and reimbursement systems and the heterogeneous information made publicly available on their decisions. Nonetheless, our study suggests that the primary purpose to grant equal availability to OMPs to the patients in the Eropean Union via the implementation of the orphan regulation was partially achieved with important variations of access observed across the countries included in our study.


2009 ◽  
pp. 1-6 ◽  
Author(s):  
Nishan Fernando ◽  
Gordon Prescott ◽  
Jennifer Cleland ◽  
Kathryn Greaves ◽  
Hamish McKenzie

1990 ◽  
Vol 35 (8) ◽  
pp. 800-801
Author(s):  
Michael F. Pogue-Geile

1992 ◽  
Vol 37 (10) ◽  
pp. 1076-1077
Author(s):  
Barbara A. Gutek

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