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  1. Article ; Online: Duration of intravenous antibiotic therapy in people with cystic fibrosis.

    Abbott, Linsey / Plummer, Amanda / Hoo, Zhe Hui / Wildman, Martin

    The Cochrane database of systematic reviews

    2019  Volume 9, Page(s) CD006682

    Abstract: Background: Progressive lung damage from recurrent exacerbations is the major cause of mortality and morbidity in cystic fibrosis. Life expectancy of people with cystic fibrosis has increased dramatically in the last 40 years. One of the major reasons ... ...

    Abstract Background: Progressive lung damage from recurrent exacerbations is the major cause of mortality and morbidity in cystic fibrosis. Life expectancy of people with cystic fibrosis has increased dramatically in the last 40 years. One of the major reasons for this increase is the mounting use of antibiotics to treat chest exacerbations caused by bacterial infections. The optimal duration of intravenous antibiotic therapy is not clearly defined. Individuals usually receive intravenous antibiotics for 14 days, but treatment may range from 10 to 21 days. A shorter duration of antibiotic treatment risks inadequate clearance of infection which could lead to further lung damage. Prolonged courses of intravenous antibiotics are expensive and inconvenient. The risk of systemic side effects such as allergic reactions to antibiotics also increases with prolonged courses and the use of aminoglycosides requires frequent monitoring to minimise some of their side effects. However, some organisms which infect people with cystic fibrosis are known to be multi-resistant to antibiotics, and may require a longer course of treatment. This is an update of previously published reviews.
    Objectives: To assess the optimal duration of intravenous antibiotic therapy for treating chest exacerbations in people with cystic fibrosis.
    Search methods: We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group Trials Register which comprises references identified from comprehensive electronic database searches, handsearches of relevant journals, abstract books and conference proceedings. Most recent search of the Group's Cystic Fibrosis Trials Register: 30 May 2019.We also searched online trials registries. Most recent search of the ClinicalTrials.gov and WHO International Clinical Trials Registry Platform (ICTRP) portal: 06 January 2019.
    Selection criteria: Randomised and quasi-randomised controlled trials comparing different durations of intravenous antibiotic courses for acute respiratory exacerbations in people with CF, either with the same drugs at the same dosage, the same drugs at a different dosage or frequency or different antibiotics altogether, including studies with additional therapeutic agents.
    Data collection and analysis: No eligible trials were identified for inclusion. A trial looking at the standardised treatment of pulmonary exacerbations is currently ongoing and will be included when the results are published.  MAIN RESULTS: No eligible trials were included.
    Authors' conclusions: There are no clear guidelines on the optimum duration of intravenous antibiotic treatment. Duration of treatment is currently based on unit policies and response to treatment. Shorter duration of treatment should improve quality of life and adherence, result in a reduced incidence of drug reactions and be less costly. However, the shorter duration may not be sufficient to clear a chest infection and may result in an early recurrence of an exacerbation. This systematic review identifies the need for a multicentre, randomised controlled trial comparing different durations of intravenous antibiotic treatment as it has important clinical and financial implications. The currently ongoing STOP2 trial is expected to provide some guidance on these questions when published.
    MeSH term(s) Anti-Bacterial Agents/therapeutic use ; Bacterial Infections/drug therapy ; Bacterial Infections/etiology ; Cystic Fibrosis/complications ; Cystic Fibrosis/drug therapy ; Humans ; Injections, Intravenous ; Quality of Life ; Respiratory Tract Infections/drug therapy ; Respiratory Tract Infections/etiology
    Chemical Substances Anti-Bacterial Agents
    Language English
    Publishing date 2019-09-05
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Systematic Review
    ISSN 1469-493X
    ISSN (online) 1469-493X
    DOI 10.1002/14651858.CD006682.pub6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Duration of intravenous antibiotic therapy in people with cystic fibrosis.

    Plummer, Amanda / Wildman, Martin

    The Cochrane database of systematic reviews

    2013  , Issue 5, Page(s) CD006682

    Abstract: Background: Respiratory disease is the major cause of mortality and morbidity in cystic fibrosis (CF). Life expectancy of people with CF has increased dramatically in the last 40 years. One of the major reasons for this increase is the mounting use of ... ...

    Abstract Background: Respiratory disease is the major cause of mortality and morbidity in cystic fibrosis (CF). Life expectancy of people with CF has increased dramatically in the last 40 years. One of the major reasons for this increase is the mounting use of antibiotics to treat chest exacerbations caused by bacterial infections. The optimal duration of intravenous antibiotic therapy is not clearly defined. Individuals usually receive intravenous antibiotics for 14 days, but treatment may range from 10 to 21 days. A shorter duration of antibiotic treatment risks inadequate clearance of infection which could lead to further lung damage. Prolonged courses of intravenous antibiotics are expensive and inconvenient and the incidence of allergic reactions to antibiotics also increases with prolonged courses. The use of aminoglycosides requires frequent monitoring to avoid some of their side effects. However, some organisms which infect people with CF are known to be multi-resistant to antibiotics, and may require a longer course of treatment.
    Objectives: To assess the optimal duration of intravenous antibiotic therapy for treating chest exacerbations in people with cystic fibrosis.
    Search methods: We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group Trials Register which comprises references identified from comprehensive electronic database searches, handsearches of relevant journals, abstract books and conference proceedings.Most recent search of the Group's Cystic Fibrosis Trials Register: 15 November 2012.
    Selection criteria: Randomised and quasi-randomised controlled trials comparing different durations of intravenous antibiotic courses for acute respiratory exacerbations in people with CF, either with the same drugs at the same dosage, the same drugs at a different dosage or frequency or different antibiotics altogether, including studies with additional therapeutic agents.
    Data collection and analysis: No eligible trials were identified.
    Main results: No eligible trials were identified.
    Authors' conclusions: There are no clear guidelines on the optimum duration of intravenous antibiotic treatment. Duration of treatment is currently based on unit policies and response to treatment. Shorter duration of treatment should improve quality of life and compliance; result in a reduced incidence of drug reactions; and be less costly. However, this may not be sufficient to clear a chest infection and may result in an early recurrence of an exacerbation. This systematic review identifies the need for a multicentre, randomised controlled trial comparing different durations of intravenous antibiotic treatment as it has important clinical and financial implications.
    MeSH term(s) Anti-Bacterial Agents/administration & dosage ; Bacterial Infections/drug therapy ; Cystic Fibrosis/complications ; Drug Administration Schedule ; Humans ; Injections, Intravenous ; Lung Diseases/drug therapy
    Chemical Substances Anti-Bacterial Agents
    Language English
    Publishing date 2013-05-31
    Publishing country England
    Document type Journal Article ; Review
    ISSN 1469-493X
    ISSN (online) 1469-493X
    DOI 10.1002/14651858.CD006682.pub4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Duration of intravenous antibiotic therapy in people with cystic fibrosis.

    Plummer, Amanda / Wildman, Martin / Gleeson, Tim

    The Cochrane database of systematic reviews

    2016  Volume 9, Page(s) CD006682

    Abstract: Background: Respiratory disease is the major cause of mortality and morbidity in cystic fibrosis. Life expectancy of people with cystic fibrosis has increased dramatically in the last 40 years. One of the major reasons for this increase is the mounting ... ...

    Abstract Background: Respiratory disease is the major cause of mortality and morbidity in cystic fibrosis. Life expectancy of people with cystic fibrosis has increased dramatically in the last 40 years. One of the major reasons for this increase is the mounting use of antibiotics to treat chest exacerbations caused by bacterial infections. The optimal duration of intravenous antibiotic therapy is not clearly defined. Individuals usually receive intravenous antibiotics for 14 days, but treatment may range from 10 to 21 days. A shorter duration of antibiotic treatment risks inadequate clearance of infection which could lead to further lung damage. Prolonged courses of intravenous antibiotics are expensive and inconvenient and the incidence of allergic reactions to antibiotics also increases with prolonged courses. The use of aminoglycosides requires frequent monitoring to avoid some of their side effects. However, some organisms which infect people with cystic fibrosis are known to be multi-resistant to antibiotics, and may require a longer course of treatment. This is an update of previously published reviews.
    Objectives: To assess the optimal duration of intravenous antibiotic therapy for treating chest exacerbations in people with cystic fibrosis.
    Search methods: We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group Trials Register which comprises references identified from comprehensive electronic database searches, handsearches of relevant journals, abstract books and conference proceedings.Most recent search of the Group's Cystic Fibrosis Trials Register: 05 May 2016.
    Selection criteria: Randomised and quasi-randomised controlled trials comparing different durations of intravenous antibiotic courses for acute respiratory exacerbations in people with CF, either with the same drugs at the same dosage, the same drugs at a different dosage or frequency or different antibiotics altogether, including studies with additional therapeutic agents.
    Data collection and analysis: No eligible trials were identified.
    Main results: No eligible trials were identified.
    Authors' conclusions: There are no clear guidelines on the optimum duration of intravenous antibiotic treatment. Duration of treatment is currently based on unit policies and response to treatment. Shorter duration of treatment should improve quality of life and compliance; result in a reduced incidence of drug reactions; and be less costly. However, this may not be sufficient to clear a chest infection and may result in an early recurrence of an exacerbation. This systematic review identifies the need for a multicentre, randomised controlled trial comparing different durations of intravenous antibiotic treatment as it has important clinical and financial implications.
    Language English
    Publishing date 2016-09-01
    Publishing country England
    Document type Journal Article ; Review
    ISSN 1469-493X
    ISSN (online) 1469-493X
    DOI 10.1002/14651858.CD006682.pub5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Duration of intravenous antibiotic therapy in people with cystic fibrosis.

    Plummer, Amanda / Wildman, Martin

    The Cochrane database of systematic reviews

    2011  , Issue 1, Page(s) CD006682

    Abstract: Background: Respiratory disease is the major cause of mortality and morbidity in cystic fibrosis (CF). Life expectancy of people with CF has increased dramatically in the last 40 years. One of the major reasons for this increase is the mounting use of ... ...

    Abstract Background: Respiratory disease is the major cause of mortality and morbidity in cystic fibrosis (CF). Life expectancy of people with CF has increased dramatically in the last 40 years. One of the major reasons for this increase is the mounting use of antibiotics to treat chest exacerbations caused by bacterial infections. The optimal duration of intravenous antibiotic therapy is not clearly defined. Individuals usually receive intravenous antibiotics for 14 days, but treatment may range from 10 to 21 days. A shorter duration of antibiotic treatment risks inadequate clearance of infection which could lead to further lung damage. Prolonged courses of intravenous antibiotics are expensive and inconvenient and the incidence of allergic reactions to antibiotics also increases with prolonged courses. The use of aminoglycosides requires frequent monitoring to avoid some of their side effects. However, some organisms which infect people with CF are known to be multi-resistant to antibiotics, and may require a longer course of treatment.
    Objectives: To assess the optimal duration of intravenous antibiotic therapy for treating chest exacerbations in people with cystic fibrosis.
    Search strategy: We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group Trials Register which comprises references identified from comprehensive electronic database searches, handsearches of relevant journals, abstract books and conference proceedings.Most recent search of the Group's Cystic Fibrosis Trials Register: 3 December 2010.
    Selection criteria: Randomised and quasi-randomised controlled trials comparing different durations of intravenous antibiotic courses for acute respiratory exacerbations in people with CF, either with the same drugs at the same dosage, the same drugs at a different dosage or frequency or different antibiotics altogether, including studies with additional therapeutic agents.
    Data collection and analysis: No eligible trials were identified.
    Main results: No eligible trials were identified.
    Authors' conclusions: There are no clear guidelines on the optimum duration of intravenous antibiotic treatment. Duration of treatment is currently based on unit policies and response to treatment. Shorter duration of treatment should improve quality of life and compliance; result in a reduced incidence of drug reactions; and be less costly. However, this may not be sufficient to clear a chest infection and may result in an early recurrence of an exacerbation. This systematic review identifies the need for a multicentre, randomised controlled trial comparing different durations of intravenous antibiotic treatment as it has important clinical and financial implications.
    MeSH term(s) Anti-Bacterial Agents/administration & dosage ; Bacterial Infections/drug therapy ; Cystic Fibrosis/complications ; Drug Administration Schedule ; Humans ; Injections, Intravenous ; Lung Diseases/drug therapy
    Chemical Substances Anti-Bacterial Agents
    Language English
    Publishing date 2011-01-19
    Publishing country England
    Document type Journal Article ; Review
    ISSN 1469-493X
    ISSN (online) 1469-493X
    DOI 10.1002/14651858.CD006682.pub3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Corrigendum to "Using a learning health system to understand the mismatch between medicines supply and actual medicines use among adults with cystic fibrosis" [J Cyst Fibros (2022), 21/2, 323-331].

    Bevan, Amanda / Hoo, Zhe Hui / Totton, Nikki / Girling, Carla / Davids, India R / Whelan, Pauline / Antrobus, Steven / Ainsworth, John / Buchan, Iain / Anderson, Alan / Bourke, Stephen / Doe, Simon / Echevarria, Carlos / Taylor, Jill / Bell, Nicholas J / Bateman, Kathryn / Jones, Carys / Moran, Peter / Fitch, Giles /
    Martin, Michael / McGowan, Angela / Morrow, Stephen / Seabridge, Heather / Bush, Nicki / Daniels, Tracey / Lee, Katy / Robson, Nicola / Shiferaw, Dejene / Sweis, Dimah / Thomas, Rebecca / Faulkner, Jayne / Flight, William G / Poole, Sarah / Warnock, Louise / Allenby, Mark I / Carroll, Mary / Daniels, Thomas V / Dunn, Helen / Nightingale, Julia A / Shepherd, Elizabeth / Ohri, Chandra / Gadsby, Jessica / Range, Simon / Tature, Darren / Barr, Helen L / Dawson, Sophie / Dewar, Jane / Miller, Bryony / Saini, Gauri / Galey, Penny / Johnson, Jack / Pasteur, Mark C / Derry, David / Gledhill, Harriet / Lawson, Angharad / Thomas, Michelle / Waine, David / Cunningham, Josie / Damani, Annant / Higton, Alexandra / Orchard, Christopher / Carolan, Charlotte / Tahir, Misbah / Plummer, Amanda / Hutchings, Marlene / Edenborough, Frank P / Curley, Rachael / Wildman, Martin J

    Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

    2022  Volume 21, Issue 5, Page(s) 893–897

    Language English
    Publishing date 2022-07-28
    Publishing country Netherlands
    Document type Published Erratum
    ZDB-ID 2084724-5
    ISSN 1873-5010 ; 1569-1993
    ISSN (online) 1873-5010
    ISSN 1569-1993
    DOI 10.1016/j.jcf.2022.07.011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Using a learning health system to understand the mismatch between medicines supply and actual medicines use among adults with cystic fibrosis.

    Bevan, Amanda / Hoo, Zhe Hui / Totton, Nikki / Girling, Carla / Davids, India R / Whelan, Pauline / Antrobus, Steven / Ainsworth, John / Buchan, Iain / Anderson, Alan / Bourke, Stephen / Doe, Simon / Echevarria, Carlos / Taylor, Jill / Bell, Nicholas J / Bateman, Kathryn / Jones, Carys / Moran, Peter / Fitch, Giles /
    Martin, Michael / McGowan, Angela / Morrow, Stephen / Seabridge, Heather / Bush, Nicki / Daniels, Tracey / Lee, Katy / Robson, Nicola / Shiferaw, Dejene / Sweis, Dimah / Thomas, Rebecca / Faulkner, Jayne / Flight, William G / Poole, Sarah / Warnock, Louise / Allenby, Mark I / Carroll, Mary / Daniels, Thomas V / Dunn, Helen / Nightingale, Julia A / Shepherd, Elizabeth / Ohri, Chandra / Gadsby, Jessica / Range, Simon / Tature, Darren / Barr, Helen L / Dawson, Sophie / Dewar, Jane / Miller, Bryony / Saini, Gauri / Galey, Penny / Johnson, Jack / Pasteur, Mark C / Derry, David / Gledhill, Harriet / Lawson, Angharad / Thomas, Michelle / Waine, David / Cunningham, Josie / Damani, Annant / Higton, Alexandra / Orchard, Christopher / Carolan, Charlotte / Tahir, Misbah / Plummer, Amanda / Hutchings, Marlene / Edenborough, Frank P / Curley, Rachael / Wildman, Martin J

    Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

    2021  Volume 21, Issue 2, Page(s) 323–331

    Abstract: Background: Studies in separate cohorts suggest possible discrepancies between inhaled medicines supplied (median 50-60%) and medicines used (median 30-40%). We performed the first study that directly compares CF medicine supply against use to identify ... ...

    Abstract Background: Studies in separate cohorts suggest possible discrepancies between inhaled medicines supplied (median 50-60%) and medicines used (median 30-40%). We performed the first study that directly compares CF medicine supply against use to identify the cost of excess medicines supply.
    Methods: This cross-sectional study included participants from 12 UK adult centres with ≥1 year of continuous adherence data from data-logging nebulisers. Medicine supply was measured as medication possession ratio (MPR) for a 1-year period from the first suitable supply date. Medicine use was measured as electronic data capture (EDC) adherence over the same period. The cost of excess medicines was calculated as whole excess box(es) supplied after accounting for the discrepancy between EDC adherence and MPR with 20% contingency.
    Results: Among 275 participants, 133 (48.4%) were females and mean age was 30 years (95% CI 29-31 years). Median EDC adherence was 57% (IQR 23-86%), median MPR was 74% (IQR 46-96%) and the discrepancy between measures was median 14% (IQR 2-29%). Even with 20% contingency, mean potential cost of excess medicines was £1,124 (95% CI £855-1,394), ranging from £183 (95% CI £29-338) for EDC adherence ≥80% to £2,017 (95% CI £1,507-2,526) for EDC adherence <50%.
    Conclusions: This study provides a conservative estimate of excess inhaled medicines supply cost among adults with CF in the UK. The excess supply cost was highest among those with lowest EDC adherence, highlighting the importance of adherence support and supplying medicine according to actual use. MPR provides information about medicine supply but over-estimates actual medicine use.
    MeSH term(s) Adult ; Cross-Sectional Studies ; Cystic Fibrosis/drug therapy ; Cystic Fibrosis/epidemiology ; Female ; Humans ; Learning Health System ; Medication Adherence ; Nebulizers and Vaporizers ; Retrospective Studies
    Language English
    Publishing date 2021-09-23
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2084724-5
    ISSN 1873-5010 ; 1569-1993
    ISSN (online) 1873-5010
    ISSN 1569-1993
    DOI 10.1016/j.jcf.2021.09.007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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