Theodore Konstantine Marras
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
Theodore Konstantine Marras has a total of 121 co-authors. Here are the top co-authors by number of shared publications:
Sarah K. Brode
Department of Medicine, University of Toronto, Toronto, Canada; Division of Respirology, Toronto Western Hospital, Toronto, Canada
8 shared publicationsFrances B. Jamieson
Laboratory Services, Public Health Ontario, Toronto, Ontario, Canada
7 shared publications- Sarah Kathleen Brode
Department of Medicine, University of Toronto , Toronto, Ontario
5 shared publications - Alex Marchand-Austin
Public Health Ontario, Toronto, Ontario, Canada
4 shared publications - D. Rebecca Prevots
Epidemiology and Population Studies Unit, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, USA
3 shared publications Jeffrey C. Kwong
3 shared publications
Latest Publications
- 14 August 2023
- Published by Elsevier in Clinics in Chest Medicine
- Vol. 44 (4) , 799-813
Treatment of the Less Common Nontuberculous Mycobacterial Pulmonary Disease
- 14 August 2023
- Published by Elsevier in Clinics in Chest Medicine
- Vol. 44 (4) , 799-813
Treatment of the Less Common Nontuberculous Mycobacterial Pulmonary Disease
- Open Access
- 9 January 2023
- Published by Elsevier in Tuberculosis
- Vol. 139, 102305
Environmental risk of nontuberculous mycobacterial infection: Strategies for advancing methodology
- 9 January 2023
- Published by Elsevier in Tuberculosis
- Vol. 139, 102305
Open AccessEnvironmental risk of nontuberculous mycobacterial infection: Strategies for advancing methodology
- Open Access
- 17 March 2022
- Published by European Respiratory Society (ERS) in ERJ Open Research
- Vol. 8 (3)
Amikacin liposome inhalation suspension clinical benefit–risk assessment for refractoryMycobacterium aviumcomplex lung disease
Marraset al. report a low number needed to treat and high number needed to harm supporting addition of amikacin liposome inhalation suspension to guideline-based treatments in patients with treatment-refractory Mycobacterium avium complex lung diseasehttps://bit.ly/3tPFW7D
- 17 March 2022
- Published by European Respiratory Society (ERS) in ERJ Open Research
- Vol. 8 (3)
Open AccessAmikacin liposome inhalation suspension clinical benefit–risk assessment for refractoryMycobacterium aviumcomplex lung disease
Marraset al. report a low number needed to treat and high number needed to harm supporting addition of amikacin liposome inhalation suspension to guideline-based treatments in patients with treatment-refractory Mycobacterium avium complex lung diseasehttps://bit.ly/3tPFW7D
- 1 April 2021
- Published by Elsevier in Respiratory Medicine
- Vol. 179, 106338
Aspergillus isolation in nontuberculous mycobacterial pulmonary disease: Associated with antimycobacterial treatment initiation but not response
- 1 April 2021
- Published by Elsevier in Respiratory Medicine
- Vol. 179, 106338
Aspergillus isolation in nontuberculous mycobacterial pulmonary disease: Associated with antimycobacterial treatment initiation but not response
- 10 March 2020
- Published by University of Toronto Press Inc. (UTPress) in Journal of the Association of Medical Microbiology and Infectious Disease Canada
- Vol. 5 (2) , 77-86
Underutilization of nontuberculous mycobacterial drug susceptibility testing in Ontario, Canada, 2010–2015
Background: Drug susceptibility testing (DST) in nontuberculous mycobacterial pulmonary disease (NTM-PD) is useful for some Mycobacterium species. International guidelines recommend routine use of DST for clinically relevant mycobacteria. DST use and results are poorly studied at the population level. We sought to identify the frequency of DST utilization for nontuberculous mycobacteria (NTMs) and describe the potential relevance of these results in Ontario. Methods: Using public health laboratory data, we performed a population-based retrospective analysis of NTM DST utilization in Ontario from May 2010 to June 2015. We determined the proportion of incident NTM-PD infections for which DST was performed and analyzed minimum inhibitory concentration (MIC) distributions from NTM testing overall, using thresholds recommended by the Clinical and Laboratory Standards Institute. Results: The proportion of incident cases of NTM-PD tested for DST was 6.3% (240/3,806) for Mycobacterium avium complex (MAC), 36.2% (67/185) for M. abscessus, and 1.8% (19/1,057) for M. xenopi. Among specimens from all body sites, MAC resistance to clarithromycin occurred in 8.0% of specimens (21/262) and MAC resistance to amikacin (intravenous, MIC > 64 µg/mL) occurred in 22.6% (19/84). M. abscessus resistance occurred as follows: to amikacin, 3.8% (3/79); cefoxitin, 14.0% (11/79); imipenem, 30.4% (14/46); linezolid, 39.2% (31/79); clarithromycin, 54.2% (13/24); ciprofloxacin, 92.4% (73/79); and moxifloxacin, 91.1% (51/56). M. xenopi analysis was limited by few DST requests and a lack of DST clinical correlation. Conclusions: We found that NTM DST is underutilized in Ontario and observed a very high frequency of amikacin resistance among MAC isolates.
- 10 March 2020
- Published by University of Toronto Press Inc. (UTPress) in Journal of the Association of Medical Microbiology and Infectious Disease Canada
- Vol. 5 (2) , 77-86
Underutilization of nontuberculous mycobacterial drug susceptibility testing in Ontario, Canada, 2010–2015
Background: Drug susceptibility testing (DST) in nontuberculous mycobacterial pulmonary disease (NTM-PD) is useful for some Mycobacterium species. International guidelines recommend routine use of DST for clinically relevant mycobacteria. DST use and results are poorly studied at the population level. We sought to identify the frequency of DST utilization for nontuberculous mycobacteria (NTMs) and describe the potential relevance of these results in Ontario. Methods: Using public health laboratory data, we performed a population-based retrospective analysis of NTM DST utilization in Ontario from May 2010 to June 2015. We determined the proportion of incident NTM-PD infections for which DST was performed and analyzed minimum inhibitory concentration (MIC) distributions from NTM testing overall, using thresholds recommended by the Clinical and Laboratory Standards Institute. Results: The proportion of incident cases of NTM-PD tested for DST was 6.3% (240/3,806) for Mycobacterium avium complex (MAC), 36.2% (67/185) for M. abscessus, and 1.8% (19/1,057) for M. xenopi. Among specimens from all body sites, MAC resistance to clarithromycin occurred in 8.0% of specimens (21/262) and MAC resistance to amikacin (intravenous, MIC > 64 µg/mL) occurred in 22.6% (19/84). M. abscessus resistance occurred as follows: to amikacin, 3.8% (3/79); cefoxitin, 14.0% (11/79); imipenem, 30.4% (14/46); linezolid, 39.2% (31/79); clarithromycin, 54.2% (13/24); ciprofloxacin, 92.4% (73/79); and moxifloxacin, 91.1% (51/56). M. xenopi analysis was limited by few DST requests and a lack of DST clinical correlation. Conclusions: We found that NTM DST is underutilized in Ontario and observed a very high frequency of amikacin resistance among MAC isolates.
- Open Access
- 10 June 2019
- Published by Taylor & Francis in Journal of Medical Economics
- Vol. 22 (11) , 1126-1133
Guidelines-based treatment associated with improved economic outcomes in nontuberculous mycobacterial lung disease
Background: The prevalence of nontuberculous mycobacterial lung disease (NTMLD) in the United States (US) has increased; however, data characterizing the associated healthcare utilization and expenditure at the national level are limited. Objective: To examine associations between economic outcomes and the use of anti-Mycobacterium avium complex (MAC) guidelines-based treatment (GBT) for newly diagnosed NTMLD in a US national managed care claims database (Optum® Clinformatics® Data Mart). Methods: NTMLD was defined as having ≥2 claims for NTMLD (ICD-9 031.0; ICD-10 A31.0) on separate occasions ≥30 days apart (between 2007 and 2016). The cohort included patients insured continuously over a period of at least 36 months (12 months before initial NTMLD diagnostic claim and for the subsequent 24 months). Treatment was classified as GBT (consistent with American Thoracic Society/Infectious Diseases Society of America guidelines), non-GBT, or untreated. All-cause hospitalization rates and total healthcare expenditures at Year 2 were assessed as outcomes of the treatment prescribed in Year 1 after NTMLD diagnosis. Results: A total of 1039 patients met study criteria for NTMLD (GBT, n = 294; non-GBT, n = 298; untreated, n = 447). After adjustment for baseline characteristics, GBT was associated with a significantly lower all-cause hospitalization risk versus non-GBT (odds ratio [OR] = 0.53; 95% CI, 0.33-0.85, P = 0.008), and versus being untreated (OR =0.57; 95% CI, 0.35-0.91, P = 0.020). Adjusted total healthcare expenditure in Year 2 with GBT ($69,691) was lower than that with non-GBT ($77,624) with a difference of −$7933 (95% CI, −$14,968 to −$899; P = 0.03). Conclusions: Patients with NTMLD in a US managed claims database who were prescribed GBT had lower hospitalization risk than those who were prescribed non-GBT or were untreated. GBT was associated with lower total healthcare expenditure compared with non-GBT.
- 10 June 2019
- Published by Taylor & Francis in Journal of Medical Economics
- Vol. 22 (11) , 1126-1133
Open AccessGuidelines-based treatment associated with improved economic outcomes in nontuberculous mycobacterial lung disease
Background: The prevalence of nontuberculous mycobacterial lung disease (NTMLD) in the United States (US) has increased; however, data characterizing the associated healthcare utilization and expenditure at the national level are limited. Objective: To examine associations between economic outcomes and the use of anti-Mycobacterium avium complex (MAC) guidelines-based treatment (GBT) for newly diagnosed NTMLD in a US national managed care claims database (Optum® Clinformatics® Data Mart). Methods: NTMLD was defined as having ≥2 claims for NTMLD (ICD-9 031.0; ICD-10 A31.0) on separate occasions ≥30 days apart (between 2007 and 2016). The cohort included patients insured continuously over a period of at least 36 months (12 months before initial NTMLD diagnostic claim and for the subsequent 24 months). Treatment was classified as GBT (consistent with American Thoracic Society/Infectious Diseases Society of America guidelines), non-GBT, or untreated. All-cause hospitalization rates and total healthcare expenditures at Year 2 were assessed as outcomes of the treatment prescribed in Year 1 after NTMLD diagnosis. Results: A total of 1039 patients met study criteria for NTMLD (GBT, n = 294; non-GBT, n = 298; untreated, n = 447). After adjustment for baseline characteristics, GBT was associated with a significantly lower all-cause hospitalization risk versus non-GBT (odds ratio [OR] = 0.53; 95% CI, 0.33-0.85, P = 0.008), and versus being untreated (OR =0.57; 95% CI, 0.35-0.91, P = 0.020). Adjusted total healthcare expenditure in Year 2 with GBT ($69,691) was lower than that with non-GBT ($77,624) with a difference of −$7933 (95% CI, −$14,968 to −$899; P = 0.03). Conclusions: Patients with NTMLD in a US managed claims database who were prescribed GBT had lower hospitalization risk than those who were prescribed non-GBT or were untreated. GBT was associated with lower total healthcare expenditure compared with non-GBT.