| Literature DB >> 33034142 |
Jemma Haines1,2, Karen Esposito3, Claire Slinger4, Nicola Pargeter5, Jennifer Murphy6, Julia Selby7, Kathryn Prior4, Adel Mansur5, Aashish Vyas4, Andrew E Stanton6, Ian Sabroe3, James H Hull7,8,9, Stephen J Fowler1,2.
Abstract
Prior to the COVID-19 pandemic, laryngoscopy was the mandatory gold standard for the accurate assessment and diagnosis of inducible laryngeal obstruction. However, upper airway endoscopy is considered an aerosol-generating procedure in professional guidelines, meaning routine procedures are highly challenging and the availability of laryngoscopy is reduced. In response, we have convened a multidisciplinary panel with broad experience in managing this disease and agreed a recommended strategy for presumptive diagnosis in patients who cannot have laryngoscopy performed due to pandemic restrictions. To maintain clinical standards whilst ensuring patient safety, we discuss the importance of triage, information gathering, symptom assessment and early review of response to treatment. The consensus recommendations will also be potentially relevant to other future situations where access to laryngoscopy is restricted, although we emphasize that this investigation remains the gold standard.Entities:
Keywords: COVID-19; inducible laryngeal obstruction; laryngoscopy
Mesh:
Year: 2020 PMID: 33034142 PMCID: PMC7675451 DOI: 10.1111/cea.13745
Source DB: PubMed Journal: Clin Exp Allergy ISSN: 0954-7894 Impact factor: 5.018
Figure 1Clinical pathway for suspected inducible laryngeal obstruction in light of COVID‐19. *For “red flag” symptoms see text; †for example clinical symptoms/Vocal Cord Dysfunction Questionnaire/visual analogue scale; ‡ see Table 1. Abbreviations: ENT—ear nose and throat; MDT—multidisciplinary team; SLT—speech and language therapy; RAG—red/amber/green risk assessment, see Table 2
Suggested data set to facilitate triage/ MDT review. We acknowledge that different levels of data will be available dependent on the referral course (primary, secondary care) and may be particularly restricted if symptom onset occurred during the COVID‐19 pandemic
| Presentation | Evidence of ILO (eg screening questionnaire data and patient‐held video/ audio recordings made during symptomatic episodes) |
| Evaluation of co‐morbidities (eg asthma, reflux, nasal disease, voice disorder, cough and breathing pattern disorder) | |
| Drug history and current medications | |
| Investigations | Physiology (eg spirometry ± reversibility, flow volume loop and exercise physiology) |
| Data related to allergy (eg IgE, skin prick test results) and inflammation (eg blood/ sputum eosinophils and fractional exhaled nitric oxide) | |
| Imaging (HRCT scans, chest X‐rays) | |
| Endoscopy (bronchoscopy and laryngoscopy) | |
| Correspondence | Copies of relevant speciality letters (in particular ENT, respiratory, gastroenterology and allergy) |
| Historical questionnaire data [eg ACQ, |
Guide to recommended prioritization (red, amber, green risk ratings) of patients for laryngoscopy (adapted from 24)
| Priority | Selection criteria |
|---|---|
|
High (acute) Risk rating = RED see Figure |
Urgent diagnosis required to prevent inappropriate tracheostomy, unnecessary ITU admission/intubation or to expedite discharge Severe, unrelenting known/ presumed ILO not responding to therapy |
|
High (outpatient) Risk rating = RED see Figure |
Previous intubation due to suspected ILO Previous ITU admissions due to suspected ILO Frequent hospital admissions with suspected ILO High healthcare utilization Frequent courses of systemic corticosteroids, without expected response Significant patient distress Pre‐surgical upper airway assessment, including in the context of exercise‐ILO surgery (as appropriate) |
|
Medium Risk rating = AMBER see Figure |
Symptoms have significant impact on daily function Frequent or severe ILO episodes Undergoing assessment for biological therapy for severe asthma, with high suspicion of ILO ILO with sequelae (eg high respiratory medication burden) ILO with associated significant dysphagia (where malignancy is not suspected) |
|
Low Risk rating = GREEN see Figure |
Suspected ILO not meeting the above criteria |