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  1. Article ; Online: Perspectives of mild asthma patients on maintenance versus as-needed preventer treatment regimens: a qualitative study.

    Foster, Juliet / Beasley, Richard / Braithwaite, Irene / Harrison, Tim / Holliday, Mark / Pavord, Ian / Reddel, Helen

    BMJ open

    2022  Volume 12, Issue 1, Page(s) e048537

    Abstract: Objectives: As-needed low-dose combination budesonide-formoterol is recommended by asthma guidelines in many countries as an alternative to maintenance inhaled corticosteroids (ICS) for treatment of mild asthma, but there are few data on patient ... ...

    Abstract Objectives: As-needed low-dose combination budesonide-formoterol is recommended by asthma guidelines in many countries as an alternative to maintenance inhaled corticosteroids (ICS) for treatment of mild asthma, but there are few data on patient attitudes toward these regimens. This study explored the comparative implementation experiences and future treatment preferences of mild asthma patients who had experienced these two treatment regimens.
    Setting: A subgroup of adults randomised to maintenance ICS or as-needed ICS-formoterol in a multinational, 52-week open-label randomised controlled trial (NovelSTART) in mild asthma patients were interviewed to explore their motivations for treatment use during the study and their preferences for future treatment.
    Participants: Semistructured interviews were conducted with 74 participants (Maintenance group: n=39, As-needed group n=35, mean age 38 (range 19-69)) and thematically analysed from transcribed audiorecordings.
    Results: Emergent themes from analysis comprised: 'How much my asthma affects me' (how their asthma's impact affected their self-management motivation); 'What I know about asthma' (limited knowledge impeded appropriate self-management decision making); 'How much effort this treatment regimen involves for me' (treatment complexity and/or difficulty establishing a medication routine impeded implementation, particularly in the Maintenance group); and 'My beliefs about the benefits and risks of this treatment' (patients who considered their treatment as ineffective, eg, limited difference in symptoms relative to salbutamol (both groups) or slower onset of relief (As-needed group) had poor motivation to use the treatment). Due to the simplicity of the as-needed combination strategy, this was the preferred future regimen, even by patients who had not yet tried it.
    Conclusions: Key patient perspectives on the implementation of preventer treatments for mild asthma included factors relating to perceived asthma burden, disease knowledge, treatment complexity and treatment usefulness or safety. The as-needed budesonide-formoterol regimen was preferred to maintenance ICS treatment in mild asthma though patient education is urgently needed to address implementation motivation.
    Trial registration number: ACTRN12615000999538.
    MeSH term(s) Administration, Inhalation ; Adult ; Anti-Asthmatic Agents/therapeutic use ; Asthma/drug therapy ; Bronchodilator Agents ; Budesonide ; Budesonide, Formoterol Fumarate Drug Combination ; Humans
    Chemical Substances Anti-Asthmatic Agents ; Bronchodilator Agents ; Budesonide, Formoterol Fumarate Drug Combination ; Budesonide (51333-22-3)
    Language English
    Publishing date 2022-01-21
    Publishing country England
    Document type Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 2599832-8
    ISSN 2044-6055 ; 2044-6055
    ISSN (online) 2044-6055
    ISSN 2044-6055
    DOI 10.1136/bmjopen-2020-048537
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: The carbon footprint of as-needed budesonide-formoterol in mild asthma: a post hoc analysis.

    Hatter, Lee / Holliday, Mark / Eathorne, Allie / Bruce, Pepa / Pavord, Ian D / Reddel, Helen K / Hancox, Robert J / Papi, Alberto / Weatherall, Mark / Beasley, Richard

    The European respiratory journal

    2024  

    Abstract: Introduction: The use of pressurised metered-dose inhalers (pMDIs) and asthma exacerbations necessitating healthcare reviews contribute substantially to the global carbon footprint of healthcare. It is possible that a reduction in carbon footprint could ...

    Abstract Introduction: The use of pressurised metered-dose inhalers (pMDIs) and asthma exacerbations necessitating healthcare reviews contribute substantially to the global carbon footprint of healthcare. It is possible that a reduction in carbon footprint could be achieved by switching patients with mild asthma from salbutamol pMDI reliever therapy to inhaled corticosteroid-formoterol dry powder inhaler (DPI) reliever therapy, as recommended by the Global Initiative for Asthma (GINA).
    Methods: This post hoc analysis included all 668 adult participants in the Novel START trial, who were randomised 1:1:1 to treatment with: as-needed budesonide-formoterol DPI, as-needed salbutamol pMDI, or maintenance budesonide DPI plus as-needed salbutamol pMDI. The primary outcome was carbon footprint of asthma management, expressed as kilograms of carbon dioxide equivalent emissions (kgCO
    Results: As-needed budesonide-formoterol DPI was associated with 95.8% and 93.6% lower carbon footprint compared with as-needed salbutamol pMDI (least squares mean 1.1
    Conclusions: The as-needed budesonide-formoterol DPI treatment option was associated with a markedly lower carbon footprint than as-needed salbutamol pMDI and maintenance budesonide DPI plus as-needed salbutamol pMDI.
    Language English
    Publishing date 2024-04-12
    Publishing country England
    Document type Journal Article
    ZDB-ID 639359-7
    ISSN 1399-3003 ; 0903-1936
    ISSN (online) 1399-3003
    ISSN 0903-1936
    DOI 10.1183/13993003.01705-2023
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: ICS-formoterol reliever

    Hatter, Lee / Bruce, Pepa / Braithwaite, Irene / Holliday, Mark / Fingleton, James / Weatherall, Mark / Beasley, Richard

    ERJ open research

    2021  Volume 7, Issue 1

    Abstract: Background: The Global Initiative for Asthma recommends as-needed inhaled corticosteroid (ICS)-formoterol as an alternative to maintenance ICS plus short-acting β: Methods: We performed a systematic review and meta-analysis of all randomised ... ...

    Abstract Background: The Global Initiative for Asthma recommends as-needed inhaled corticosteroid (ICS)-formoterol as an alternative to maintenance ICS plus short-acting β
    Methods: We performed a systematic review and meta-analysis of all randomised controlled trials (RCTs) comparing as-needed ICS-formoterol with maintenance ICS plus SABA. MEDLINE, Embase, the Cochrane Central Register of Controlled Trials and Clinicaltrials.gov were searched from database inception to 12 December 2019. The primary outcome was time to first severe exacerbation. RCTs were excluded if they used as-needed budesonide-formoterol as part of a maintenance and reliever regimen, or did not report on severe exacerbations. The review is registered with PROSPERO (identifier number CRD42020154680).
    Results: Four RCTs (n=8065 participants) were included in the analysis. As-needed ICS-formoterol was associated with a prolonged time to first severe exacerbation (hazard ratio 0.85, 95% CI 0.73-1.00; p=0.048) and reduced daily ICS dose (mean difference -177.3 μg, 95% CI -182.2--172.4 μg). Asthma symptom control was worse in the as-needed group (Asthma Control Questionnaire-5 mean difference 0.12, 95% CI 0.09-0.14), although this did not meet the minimal clinically important difference of 0.50 units. There was no significant difference in serious adverse events (OR 1.07, 95% CI 0.84-1.36).
    Conclusion: As-needed ICS-formoterol offers a therapeutic alternative to maintenance low-dose ICS plus SABA in asthma and may be the preferred option when prevention of severe exacerbation is the primary aim of treatment.
    Language English
    Publishing date 2021-01-25
    Publishing country England
    Document type Journal Article
    ZDB-ID 2827830-6
    ISSN 2312-0541
    ISSN 2312-0541
    DOI 10.1183/23120541.00701-2020
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: The Anti-Inflammatory Reliever (AIR) Algorithm Study: a protocol for a single-group study of an AIR stepwise approach to the treatment of adult asthma.

    Bruce, Pepa / Hatter, Lee / Houghton, Claire / Kearns, Ciléin / Holliday, Mark / Anderson, Augustus J / Eathorne, Allie / Martindale, John / Semprini, Alex / Weatherall, Mark / Pavord, Ian / Harrison, Tim / Papi, Alberto / Horne, Rob / Beasley, Richard

    ERJ open research

    2023  Volume 9, Issue 5

    Abstract: Background: The stepwise approach to long-term asthma management, which traditionally incorporates short-acting β: Objective: The aim of this study was to evaluate the AIR stepwise approach recommended by the New Zealand adolescent and adult asthma ... ...

    Abstract Background: The stepwise approach to long-term asthma management, which traditionally incorporates short-acting β
    Objective: The aim of this study was to evaluate the AIR stepwise approach recommended by the New Zealand adolescent and adult asthma guidelines, in combination with a novel algorithm for transitioning between treatment steps.
    Methods: This 52-week, open-label, single-group study will recruit 100 adults aged 18 to 75 years with mild, moderate and moderate-severe asthma (ACTRN12620001010987). Participants will be allocated to budesonide-formoterol 200/6 µg, one actuation as needed (Step 1), one actuation twice daily and as needed (Step 2), or two actuations twice daily and one as needed (Step 3). Treatment steps will be adjusted throughout the study, in response to reliever use and asthma attacks, according to a stepwise AIR algorithm. Following a 26-week period of investigator-led transitions, participants will adjust their own treatment step. The primary outcome is participant satisfaction as measured by the Global Satisfaction score of the Treatment Satisfaction Questionnaire for Medication. Secondary outcomes will assess efficacy and safety, and describe patterns of medication use and participant flow through the treatment steps.
    Conclusion: This is the first trial to assess the AIR treatment track and algorithm. The results will provide knowledge to guide the clinical use of this approach.
    Language English
    Publishing date 2023-09-25
    Publishing country England
    Document type Journal Article
    ZDB-ID 2827830-6
    ISSN 2312-0541
    ISSN 2312-0541
    DOI 10.1183/23120541.00239-2023
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Book: Fisheries management

    Holliday, Mark / Pontecorvo, Giulio

    pandemic failure, workable solutions : pandemic failure, workable solutions

    2009  

    Author's details Giulio Pontecorvo ... With contributions by Mark Holliday
    Keywords Fischereipolitik ; Fischwirtschaft ; Fischereiressourcen ; Nachhaltigkeit ; Aquakultur ; Welt
    Language English
    Size XXIV, 176 S., graph. Darst., 23cm
    Publisher Emerald
    Publishing place Bingley u.a.
    Document type Book
    ISBN 008044623X ; 9781848552166 ; 9780080446233 ; 1848552165
    Database Johann Heinrich von Thünen-Institut, Federal Research Institute for Rural Areas, Forestry and Fisheries

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  6. Book: Fisheries management

    Holliday, Mark / Pontecorvo, Giulio

    pandemic failure, workable solutions : pandemic failure, workable solutions

    2009  

    Author's details Giulio Pontecorvo ... With contributions by Mark Holliday
    Keywords Fischereipolitik ; Fischwirtschaft ; Fischereiressourcen ; Nachhaltigkeit ; Aquakultur ; Welt
    Language English
    Size XXIV, 176 S., graph. Darst., 23cm
    Publisher Emerald
    Publishing place Bingley u.a.
    Document type Book
    ISBN 008044623X ; 9781848552166 ; 9780080446233 ; 1848552165
    Database ECONomics Information System

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  7. Article: START CARE: a protocol for a randomised controlled trial of step-wise budesonide-formoterol reliever-based treatment in children.

    Barry, Tasmin / Holliday, Mark / Sparks, Jenny / Biggs, Rowan / Colman, Atalie / Lamb, Rebekah / Oldfield, Karen / Shortt, Nick / Kerse, Kyley / Martindale, John / Eathorne, Allie / Walton, Michaela / Black, Bianca / Harwood, Matire / Bruce, Pepa / Semprini, Ruth / Bush, Andrew / Fleming, Louise / Byrnes, Catherine A /
    McNamara, David / Hatter, Lee / Dalziel, Stuart R / Weatherall, Mark / Beasley, Richard

    ERJ open research

    2024  Volume 10, Issue 2

    Abstract: Background: Asthma is the most common chronic childhood respiratory condition globally. Inhaled corticosteroid (ICS)-formoterol reliever-based regimens reduce the risk of asthma exacerbations compared with conventional short-acting β: Objective: The ... ...

    Abstract Background: Asthma is the most common chronic childhood respiratory condition globally. Inhaled corticosteroid (ICS)-formoterol reliever-based regimens reduce the risk of asthma exacerbations compared with conventional short-acting β
    Objective: The study aim is to determine the efficacy and safety of budesonide-formoterol reliever alone or maintenance and reliever therapy (MART) compared with standard therapy: budesonide or budesonide-formoterol maintenance, both with terbutaline reliever, in children aged 5 to 11 years with mild, moderate and severe asthma.
    Methods: A 52-week, multicentre, open-label, parallel group, phase III, two-sided superiority RCT will recruit 400 children aged 5 to 11 years with asthma. Participants will be randomised 1:1 to either budesonide-formoterol 100/6 µg Turbuhaler reliever alone or MART; or budesonide or budesonide-formoterol Turbuhaler maintenance, with terbutaline Turbuhaler reliever. The primary outcome is moderate and severe asthma exacerbations as rate per participant per year. Secondary outcomes are asthma control, lung function, exhaled nitric oxide and treatment step change. Assessment of Turbuhaler technique and cost-effectiveness analysis are also planned.
    Conclusion: This will be the first RCT to compare the efficacy and safety of a step-wise budesonide-formoterol reliever alone or MART regimen with conventional inhaled ICS or ICS-long-acting β-agonist maintenance plus SABA reliever in children. The results will provide a much-needed evidence base for the treatment of asthma in children.
    Language English
    Publishing date 2024-04-08
    Publishing country England
    Document type Journal Article
    ZDB-ID 2827830-6
    ISSN 2312-0541
    ISSN 2312-0541
    DOI 10.1183/23120541.00897-2023
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Asthma control with ICS-formoterol reliever versus maintenance ICS and SABA reliever therapy: a post hoc analysis of two randomised controlled trials.

    Hatter, Lee / Houghton, Claire / Bruce, Pepa / Holliday, Mark / Eathorne, Allie / Pavord, Ian / Reddel, Helen K / Hancox, Robert J / Braithwaite, Irene / Oldfield, Karen / Papi, Alberto / Weatherall, Mark / Beasley, Richard

    BMJ open respiratory research

    2022  Volume 9, Issue 1

    Abstract: Background: In randomised controlled trials, as-needed inhaled corticosteroid (ICS)-formoterol reliever therapy reduces severe exacerbation risk compared with maintenance ICS plus short-acting beta: Objective: To assess the levels and changes in ... ...

    Abstract Background: In randomised controlled trials, as-needed inhaled corticosteroid (ICS)-formoterol reliever therapy reduces severe exacerbation risk compared with maintenance ICS plus short-acting beta
    Objective: To assess the levels and changes in asthma control for as-needed budesonide-formoterol versus maintenance budesonide plus SABA in post hoc analyses from the Novel START and PRACTICAL clinical trials.
    Methods: The number and proportion of participants at study end in each ACQ-5 category ('well-controlled', 'partly controlled' or 'inadequately controlled' symptoms), and in each responder category based on the minimal clinically important difference for ACQ-5 of 0.5 (improved, no change and worse) with as-needed budesonide-formoterol and maintenance budesonide plus SABA treatment were calculated.
    Results: With last observation carried forwards, 189/214 (88.3%) and 354/434 (81.6%) of patients in the budesonide-formoterol group had 'well-controlled' or 'partly controlled' symptoms at the end of the study, vs 183/214 (85.5%) and 358/431 (83.1%) in the budesonide maintenance group, for Novel START and PRACTICAL, respectively. The proportion of patients whose symptom control was either improved or unchanged from baseline was 190/214 (88.8%) and 368/434 (84.8%) for budesonide-formoterol, vs 185/214 (86.4%) and 376/431 (87.2%) for maintenance budesonide, in Novel START and PRACTICAL respectively.
    Conclusions: There were no clinically important differences in the proportions of patients with 'well-controlled' or 'partly controlled' asthma symptoms, or proportions who improved or maintained their level of control, with as-needed budesonide-formoterol versus maintenance budesonide plus SABA.
    MeSH term(s) Adolescent ; Adult ; Humans ; Adrenal Cortex Hormones/therapeutic use ; Anti-Asthmatic Agents/therapeutic use ; Asthma/drug therapy ; Bronchodilator Agents ; Budesonide/therapeutic use ; Budesonide, Formoterol Fumarate Drug Combination/therapeutic use ; Ethanolamines/therapeutic use ; Formoterol Fumarate/therapeutic use ; Randomized Controlled Trials as Topic
    Chemical Substances Adrenal Cortex Hormones ; Anti-Asthmatic Agents ; Bronchodilator Agents ; Budesonide (51333-22-3) ; Budesonide, Formoterol Fumarate Drug Combination ; Ethanolamines ; Formoterol Fumarate (W34SHF8J2K)
    Language English
    Publishing date 2022-08-24
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2736454-9
    ISSN 2052-4439 ; 2052-4439
    ISSN (online) 2052-4439
    ISSN 2052-4439
    DOI 10.1136/bmjresp-2022-001271
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Combination budesonide/formoterol inhaler as sole reliever therapy in Māori and Pacific people with mild and moderate asthma.

    Hardy, Jo / Tewhaiti-Smith, Jordan / Baggott, Christina / Fingleton, James / Semprini, Alex / Holliday, Mark / Hancox, Robert J / Weatherall, Mark / Harwood, Matire

    The New Zealand medical journal

    2020  Volume 133, Issue 1520, Page(s) 61–72

    Abstract: Aim: In the PRACTICAL study, as-needed budesonide/formoterol reduced the rate of severe exacerbations compared with maintenance budesonide plus as-needed terbutaline. In a pre-specified analysis we analysed the efficacy in Māori and Pacific peoples, ... ...

    Abstract Aim: In the PRACTICAL study, as-needed budesonide/formoterol reduced the rate of severe exacerbations compared with maintenance budesonide plus as-needed terbutaline. In a pre-specified analysis we analysed the efficacy in Māori and Pacific peoples, populations with worse asthma outcomes.
    Method: The PRACTICAL study was a 52-week, open-label, parallel group, randomised controlled trial of 890 adults with mild to moderate asthma, who were randomised to budesonide/formoterol Turbuhaler 200/6mcg one actuation as required or budesonide Turbuhaler 200mcg one actuation twice daily and terbutaline Turbuhaler 250mcg two actuations as required. The primary outcome was rate of severe exacerbations. The analysis strategy was to test an ethnicity-treatment interaction term for each outcome variable.
    Results: Seventy-two participants (8%) identified as Māori, 36 participants (4%) as Pacific ethnicity. There was no evidence that ethnicity was an effect modifier for severe exacerbations (P interaction 0.70).
    Conclusion: The reduction in severe exacerbation risk with budesonide-formoterol reliever compared with maintenance budesonide was similar in Māori and Pacific adults compared with New Zealand European/Other.
    MeSH term(s) Administration, Inhalation ; Adult ; Anti-Asthmatic Agents/administration & dosage ; Anti-Asthmatic Agents/therapeutic use ; Asthma/drug therapy ; Asthma/physiopathology ; Bronchodilator Agents/administration & dosage ; Bronchodilator Agents/therapeutic use ; Budesonide/administration & dosage ; Budesonide/therapeutic use ; Budesonide, Formoterol Fumarate Drug Combination/administration & dosage ; Budesonide, Formoterol Fumarate Drug Combination/therapeutic use ; Case-Control Studies ; Disease Progression ; Drug Therapy, Combination/methods ; Ethnic Groups ; Female ; Humans ; Male ; Middle Aged ; Nebulizers and Vaporizers/standards ; New Zealand/epidemiology ; Outcome Assessment, Health Care ; Terbutaline/administration & dosage ; Terbutaline/therapeutic use ; Treatment Outcome
    Chemical Substances Anti-Asthmatic Agents ; Bronchodilator Agents ; Budesonide, Formoterol Fumarate Drug Combination ; Budesonide (51333-22-3) ; Terbutaline (N8ONU3L3PG)
    Language English
    Publishing date 2020-08-21
    Publishing country New Zealand
    Document type Clinical Trial, Phase III ; Journal Article ; Multicenter Study ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 390590-1
    ISSN 1175-8716 ; 0028-8446 ; 0110-7704
    ISSN (online) 1175-8716
    ISSN 0028-8446 ; 0110-7704
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: How big is your bubble? Characteristics of self-isolating household units ('bubbles') during the COVID-19 Alert Level 4 period in New Zealand: a cross-sectional survey.

    Kearns, Nethmi / Shortt, Nick / Kearns, Ciléin / Eathorne, Allie / Holliday, Mark / Mackle, Diane / Martindale, John / Semprini, Alex / Weatherall, Mark / Beasley, Richard / Braithwaite, Irene

    BMJ open

    2021  Volume 11, Issue 1, Page(s) e042464

    Abstract: Objective: To characterise the self-isolating household units (bubbles) during the COVID-19 Alert Level 4 lockdown in New Zealand.: Design, setting and participants: In this cross-sectional study, an online survey was distributed to a convenience ... ...

    Abstract Objective: To characterise the self-isolating household units (bubbles) during the COVID-19 Alert Level 4 lockdown in New Zealand.
    Design, setting and participants: In this cross-sectional study, an online survey was distributed to a convenience sample via Facebook advertising and the Medical Research Institute of New Zealand's social media platforms and mailing list. Respondents were able to share a link to the survey via their own social media platforms and by email. Results were collected over 6 days during Alert Level 4 from respondents living in New Zealand, aged 16 years and over.
    Main outcomes measures: The primary outcome was the mean size of a self-isolating household unit or bubble. Secondary outcomes included the mean number of households in each bubble, the proportion of bubbles containing essential workers and/or vulnerable people, and the mean number of times the home was left each week.
    Results: 14 876 surveys were included in the analysis. The mean (SD) bubble size was 3.58 (4.63) people, with mean (SD) number of households 1.26 (0.77). The proportion of bubbles containing one or more essential workers, or one or more vulnerable persons was 45.3% and 42.1%, respectively. The mean number of times individual bubble members left their home in the previous week was 12.9 (12.4). Bubbles that contained at least one vulnerable individual had fewer outings over the previous week compared with bubbles that did not contain a vulnerable person. The bubble sizes were similar by respondent ethnicity.
    Conclusion: In this New Zealand convenience sample, bubble sizes were small, mostly limited to one household, and a high proportion contained essential workers and/or vulnerable people. Understanding these characteristics from a country which achieved a low COVID-19 infection rate may help inform public health interventions during this and future pandemics.
    MeSH term(s) Adult ; COVID-19/epidemiology ; COVID-19/prevention & control ; Cross-Sectional Studies ; European Continental Ancestry Group/statistics & numerical data ; Family Characteristics/ethnology ; Female ; Humans ; Male ; Middle Aged ; New Zealand/epidemiology ; Oceanic Ancestry Group/statistics & numerical data ; Residence Characteristics/statistics & numerical data ; SARS-CoV-2 ; Surveys and Questionnaires ; Vulnerable Populations/statistics & numerical data
    Language English
    Publishing date 2021-01-28
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2599832-8
    ISSN 2044-6055 ; 2044-6055
    ISSN (online) 2044-6055
    ISSN 2044-6055
    DOI 10.1136/bmjopen-2020-042464
    Database MEDical Literature Analysis and Retrieval System OnLINE

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