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Your search keyword '"Tullis, D. Elizabeth"' showing total 2 results
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2 results on '"Tullis, D. Elizabeth"'

1. Triaging Access to Critical Care Resources in Patients with Chronic Respiratory Diseases in the Event of a Major COVID-19Surge: Key highlights from the Canadian Thoracic Society (CTS) Position Statement

Author

Gupta, Samir, Batt, Jane, Bourbeau, Jean, Chapman, Kenneth R., Gershon, Andrea, Granton, John, Hambly, Nathan, Hernandez, Paul, Kolb, Martin, Mehta, Sanjay, Mielniczuk, Lisa, Provencher, Steeve, Stephenson, Anne L., Swiston, John, Tullis, D. Elizabeth, Vozoris, Nicholas T., Wald, Joshua, Weatherald, Jason, and Bhutani, Mohit

Subjects
Canada, CFS, clinical frailty score, Critical Care, Cystic Fibrosis, Pulmonary Fibrosis, Respiratory Tract Diseases, PH, pulmonary hypertension, Article, Health Services Accessibility, Pulmonary Disease, Chronic Obstructive, Forced Expiratory Volume, PaO2, partial pressure of oxygen, Pulmonary Medicine, AE, acute exacerbation, IPF, idiopathic pulmonary fibrosis, Humans, COVID-19, 2019 novel coronavirus, Mortality, mMRC, modified Medical Research Council dyspnea scale, PaCO2, partial pressure of carbon dioxide, Societies, Medical, Pulmonary Arterial Hypertension, DLCO, diffusing capacity of the lungs for carbon monoxide, Health Care Rationing, Frailty, CTS, Canadian Thoracic Society, Patient Selection, Oxygen Inhalation Therapy, Surge Capacity, COVID-19, Prognosis, FEV1, forced expiratory volume in the first second, Respiratory Function Tests, REVEAL, Registry to Evaluate Early and Long-Term Pulmonary Arterial Hypertension Disease Management, Intensive Care Units, FVC, forced vital capacity, Chronic Disease, ILD, interstitial lung disease, Health Resources, Pulmonary Diffusing Capacity, Triage, RV, right ventricular
Published
2020

2. Hepatic Abscess due to Burkholderia (Pseudomonas) cepacia in Cystic Fibrosis

Author

Fraser, Kristin L, Hyland, Robert H, and Tullis, D Elizabeth

Subjects
congenital, hereditary, and neonatal diseases and abnormalities, Article Subject, respiratory tract diseases
Abstract

Burkholderia (Pseudomonas) cepacia has been cultured from bronchial secretions of patients with cystic fibrosis with varying frequency. The overall prevalence in patients over 18 years old at the authors’ centre in Toronto is 51%. Extrapulmonary infections are rare in nonimmunosuppressed patients with cystic fibrosis and B cepacia has been the causative organism in only three previous reports. Two patients with cystic fibrosis are described who developed hepatic abscesses clue to B cepacia. One patient is the sibling of two brothers in whom this complication was previously described.

Published
1995
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