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  1. Article: Subcutaneous infliximab CT-P13 without intravenous induction in psoriatic arthritis: A case report and pharmacokinetic considerations.

    Ditto, Maria Chiara / Parisi, Simone / Cotugno, Valentina / Barila, Diego Antonio / Lo Sardo, Luca / Cattel, Francesco / Fusaro, Enrico

    International journal of clinical pharmacology and therapeutics

    2024  Volume 62, Issue 3, Page(s) 122–125

    Abstract: Introduction: The biosimilar CT-P13, the first and only subcutaneous (SC) infliximab formulation, is recommended for patients with psoriatic arthritis (PsA) and can be administered as a maintenance treatment, to be started 4 weeks after the induction ... ...

    Abstract Introduction: The biosimilar CT-P13, the first and only subcutaneous (SC) infliximab formulation, is recommended for patients with psoriatic arthritis (PsA) and can be administered as a maintenance treatment, to be started 4 weeks after the induction treatment with 2 intravenous (IV) infliximab infusions.
    Objective: To evaluate treatment with SC infliximab without prior IV infusion induction to meet patient needs.
    Materials and methods: After approval by the ethics review board and based on the schedule approved for rheumatoid arthritis, SC induction was performed with infliximab CT-P13 120 mg weekly for 4 weeks, followed by an injection of 120 mg every 2 weeks.
    Results: After 4 months of therapy, joint symptoms were resolved, inflammation parameters were normalized (erythrocyte sedimentation rate) reduced from 42 to 16 mm/h, and C-reactive protein from 1.74 to 0.43 mg/dL), and clinical assessment parameters were improved. After 9 months of therapy, the clinical data remained stable, with no adverse events or local side effects.
    Conclusion: SC infliximab was successfully used without previous IV infusion induction. Although, to date, the induction of PsA treatment via the SC route is not foreseen, the known pharmacokinetic properties and the outcome improvements observed in our patient show that subcutaneous treatment induction, as is already done in the treatment of rheumatoid arthritis, is also possible.
    MeSH term(s) Humans ; Infliximab/adverse effects ; Arthritis, Psoriatic/drug therapy ; Treatment Outcome ; Arthritis, Rheumatoid/drug therapy ; Biosimilar Pharmaceuticals/adverse effects ; Antibodies, Monoclonal
    Chemical Substances Infliximab (B72HH48FLU) ; CT-P13 ; Biosimilar Pharmaceuticals ; Antibodies, Monoclonal
    Language English
    Publishing date 2024-01-11
    Publishing country Germany
    Document type Case Reports ; Journal Article
    ZDB-ID 124384-6
    ISSN 0946-1965 ; 0340-0026 ; 0300-9718 ; 0174-4879
    ISSN 0946-1965 ; 0340-0026 ; 0300-9718 ; 0174-4879
    DOI 10.5414/CP204388
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Medicine recovery and reuse in a hospital setting: a lesson from Italy.

    Gianino, Maria Michela / Cotugno, Valentina / Scattaglia, Marco / Colasanto, Irene / Scaldaferri, Matilde / Cattel, Francesco

    The International journal of pharmacy practice

    2022  Volume 30, Issue 6, Page(s) 554–558

    Abstract: Objectives: In 2017, a new programme was created for recovering and reusing (i) unexpired Class A medicines (i.e. dispensed either by community pharmacies or by hospitals) in hospital settings and (ii) medicines for hospital use only (Class H). The aim ... ...

    Abstract Objectives: In 2017, a new programme was created for recovering and reusing (i) unexpired Class A medicines (i.e. dispensed either by community pharmacies or by hospitals) in hospital settings and (ii) medicines for hospital use only (Class H). The aim of this study was to describe a three-year reuse programme and assess its impact on medicines cost savings.
    Methods: The setting was AOU Città della salute e della Scienza-in Turin (Italy). All the collected data referred to packages of medicines collected by/assigned to AOU for reuse over the 1 December 2017/1 December 2020 period. Retail prices were used to calculate the financial value of the medication. Costs for the time required for the reuse programme (a working group comprising a pharmacist, an administrative and a warehouse worker) were estimated.
    Key findings: A total of 10 450 boxes were recovered for reuse (corresponding to 52% of donated boxes). The total value was €1 300 000. Class H accounted for 73% (€952 000) of the total value of the recovered medicines, while they represented only 9% of the packages collected by/assigned to AOU. Estimated cost for the reuse programme was €75 806.
    Conclusions: Medicine recycling programmes with appropriate checks can be implemented to facilitate reuse of medications in hospital settings. This study provides evidence that a reuse programme reduced drug expenditures, especially regarding the Class H medications. These results contribute to the debate regarding opportunity for recycling and sustainability in medicines management.
    MeSH term(s) Humans ; Cost Savings ; Hospitals ; Italy
    Language English
    Publishing date 2022-07-19
    Publishing country England
    Document type Journal Article
    ZDB-ID 1087040-4
    ISSN 2042-7174 ; 0961-7671
    ISSN (online) 2042-7174
    ISSN 0961-7671
    DOI 10.1093/ijpp/riac056
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: An Observational Study of MDR Hospital-Acquired Infections and Antibiotic Use during COVID-19 Pandemic: A Call for Antimicrobial Stewardship Programs.

    Shbaklo, Nour / Corcione, Silvia / Vicentini, Costanza / Giordano, Susanna / Fiorentino, Denise / Bianco, Gabriele / Cattel, Francesco / Cavallo, Rossana / Zotti, Carla Maria / De Rosa, Francesco Giuseppe

    Antibiotics (Basel, Switzerland)

    2022  Volume 11, Issue 5

    Abstract: The pandemic caused by the COVID-19 virus has required major adjustments to healthcare systems, especially to infection control and antimicrobial stewardship. The objective of this study was to describe the incidence of multidrug-resistant (MDR) hospital- ...

    Abstract The pandemic caused by the COVID-19 virus has required major adjustments to healthcare systems, especially to infection control and antimicrobial stewardship. The objective of this study was to describe the incidence of multidrug-resistant (MDR) hospital-acquired infections (HAIs) and antibiotic consumption during the three waves of COVID-19 and to compare it to the period before the outbreak at Molinette Hospital, located in the City of Health and Sciences, a 1200-bed teaching hospital with surgical, medical, and intensive care units. We demonstrated an increase in MDR infections: particularly in
    Language English
    Publishing date 2022-05-20
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2681345-2
    ISSN 2079-6382
    ISSN 2079-6382
    DOI 10.3390/antibiotics11050695
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Vaccine development and technology for SARS-CoV-2: Current insight.

    Cattel, Luigi / Giordano, Susanna / Traina, Sara / Lupia, Tommaso / Corcione, Silvia / Angelone, Lorenzo / La Valle, Giovanni / De Rosa, Francesco G / Cattel, Francesco

    Journal of medical virology

    2021  Volume 94, Issue 3, Page(s) 878–896

    Abstract: Severe acute respiratory syndrome coronavirus 2 is associated with a severe respiratory disease in China, that rapidly spread across continents. Since the beginning of the pandemic, available data suggested the asymptomatic transmission and patients were ...

    Abstract Severe acute respiratory syndrome coronavirus 2 is associated with a severe respiratory disease in China, that rapidly spread across continents. Since the beginning of the pandemic, available data suggested the asymptomatic transmission and patients were treated with specific drugs with efficacy and safety data not always satisfactory. The aim of this review is to describe the vaccines developed by three companies, Pfizer-BioNTech, Moderna, and University of Oxford/AstraZeneca, in terms of both technological and pharmaceutical formulation, safety, efficacy, and immunogenicity. A critical analysis of Phases 1, 2, and 3 clinical trial results available was conducted, comparing the three vaccine candidates, underlining their similarities and differences. All candidates showed consistent efficacy and tolerability; although some differences can be noted, such as their technological formulation, temperature storage, which will be related to logistics and costs. Further studies will be necessary to evaluate long-term effects and to assess the vaccine safety and efficacy in the general population.
    MeSH term(s) COVID-19/prevention & control ; COVID-19 Vaccines ; Humans ; SARS-CoV-2 ; Technology ; Vaccine Development
    Chemical Substances COVID-19 Vaccines
    Language English
    Publishing date 2021-11-11
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 752392-0
    ISSN 1096-9071 ; 0146-6615
    ISSN (online) 1096-9071
    ISSN 0146-6615
    DOI 10.1002/jmv.27425
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Use of exogenous pulmonary surfactant in acute respiratory distress syndrome (ARDS): Role in SARS-CoV-2-related lung injury.

    Cattel, Francesco / Giordano, Susanna / Bertiond, Cecilia / Lupia, Tommaso / Corcione, Silvia / Scaldaferri, Matilde / Angelone, Lorenzo / De Rosa, Francesco Giuseppe

    Respiratory physiology & neurobiology

    2021  Volume 288, Page(s) 103645

    Abstract: Several pre-clinical and clinical trials show that exogenous pulmonary surfactant has clinical efficacy in inflammatory lung diseases, especially ARDS. By infecting type II alveolar cells, COVID-19 interferes with the production and secretion of the ... ...

    Abstract Several pre-clinical and clinical trials show that exogenous pulmonary surfactant has clinical efficacy in inflammatory lung diseases, especially ARDS. By infecting type II alveolar cells, COVID-19 interferes with the production and secretion of the pulmonary surfactant and therefore causes an increase in surface tension, which in turn can lead to alveolar collapse. The use of the pulmonary surfactant seems to be promising as an additional therapy for the treatment of ARDS. COVID-19 causes lung damage and ARDS, so beneficial effects of surfactant therapy in COVID-19-associated ARDS patients are conceivable, especially when applied early in the treatment strategy against pulmonary failure. Because of the robust anti-inflammatory and lung protective efficacy and the current urgent need for lung-supportive therapy, the exogenous pulmonary surfactant could be a valid supportive treatment of COVID-19 pneumonia patients in intensive care units in addition to the current standard of ARDS treatment.
    MeSH term(s) Administration, Inhalation ; Biological Products/therapeutic use ; COVID-19/drug therapy ; COVID-19/physiopathology ; Humans ; Peptides, Cyclic/therapeutic use ; Phospholipids/therapeutic use ; Pulmonary Surfactants/therapeutic use ; Respiratory Distress Syndrome/drug therapy ; Respiratory Distress Syndrome/physiopathology ; SARS-CoV-2
    Chemical Substances Biological Products ; Peptides, Cyclic ; Phospholipids ; Pulmonary Surfactants ; AP301 peptide (17ZS80333G) ; poractant alfa (KE3U2023NP)
    Language English
    Publishing date 2021-02-28
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 2077867-3
    ISSN 1878-1519 ; 1569-9048
    ISSN (online) 1878-1519
    ISSN 1569-9048
    DOI 10.1016/j.resp.2021.103645
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Topical cyclosporine hydrogel preparation: A new therapeutic option in the treatment of nail psoriasis.

    Gallo, Giuseppe / Mastorino, Luca / Barilà, Diego / Cattel, Francesco / Panzone, Michele / Quaglino, Pietro / Ribero, Simone / Dapavo, Paolo

    Dermatologic therapy

    2022  Volume 35, Issue 12, Page(s) e15917

    Abstract: Nail psoriasis is a chronic nail disorder that commonly affects psoriatic patients causing severe distress despite the limited body surface area. Treatments for nail psoriasis are limited, as nails are often difficult to treat with topical therapies, and ...

    Abstract Nail psoriasis is a chronic nail disorder that commonly affects psoriatic patients causing severe distress despite the limited body surface area. Treatments for nail psoriasis are limited, as nails are often difficult to treat with topical therapies, and among different systemic agents responses are unpredictable. We carried out a prospective study in order to analyze the effectiveness and tolerability of topical cyclosporine hydrogel ointment in nail psoriasis. Three patients, for a total of 44 nails, were treated with topical cyclosporine hydrogel ointment. All nails were evaluated, before starting the treatment, every 28 days and after 12 weeks of therapy, by the same dermatologists, through clinical and onychoscopic evaluations. The patients were also asked to assess on the compliance with product use. Complete response (CR) was observed in 2 of 3 patients; a partial response (PR) was observed in the other patient. Overall, 24 of 44 nails had CR and 20 had a PR. Cyclosporine hydrogel ointment has shown efficacy and safety in the treatment of nail psoriasis. The product has also been shown to be stable in composition, easy to apply and not discomfortable for the patient.
    MeSH term(s) Humans ; Cyclosporine ; Dermatologic Agents ; Ointments/therapeutic use ; Prospective Studies ; Hydrogels/therapeutic use ; Nail Diseases/diagnosis ; Nail Diseases/drug therapy ; Nail Diseases/etiology ; Psoriasis/diagnosis ; Psoriasis/drug therapy ; Psoriasis/complications
    Chemical Substances Cyclosporine (83HN0GTJ6D) ; Dermatologic Agents ; Ointments ; Hydrogels
    Language English
    Publishing date 2022-10-17
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1354801-3
    ISSN 1529-8019 ; 1396-0296
    ISSN (online) 1529-8019
    ISSN 1396-0296
    DOI 10.1111/dth.15917
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Cost-utility analysis of trabecular micro-bypass stents (TBS) in patients with mild-to-moderate open-angle Glaucoma in Italy.

    Fea, Antonio Maria / Cattel, Francesco / Gandolfi, Stefano / Buseghin, Giorgio / Furneri, Gianluca / Costagliola, Ciro

    BMC health services research

    2021  Volume 21, Issue 1, Page(s) 824

    Abstract: Background: Glaucoma is a disease characterized by progressive damage of the optic nerve. Several therapeutic options are available to lower intraocular pressure (IOP). In primary open-angle glaucoma (POAG) patients with inadequate IOP control (or ... ...

    Abstract Background: Glaucoma is a disease characterized by progressive damage of the optic nerve. Several therapeutic options are available to lower intraocular pressure (IOP). In primary open-angle glaucoma (POAG) patients with inadequate IOP control (or controlled with multiple medical therapies or for whom medical therapy is contraindicated), the implantation of micro-invasive glaucoma surgery devices (MIGS) and concomitant cataract surgery has proved to be more effective in reducing intraocular pressure (IOP), as compared to cataract surgery alone. The objective of this study was to assess the cost-effectiveness of iStent inject® device with concurrent cataract surgery vs. cataract surgery alone, in patients with mild-to-moderate POAG, adopting the Italian National Health Service (NHS) perspective.
    Methods: Simulation of outcomes and costs was undertaken using a Markov model with 4 health states and one-month cycles, that is used to simulate the prognosis of these patients. Efficacy data were obtained from the randomized clinical trial (RCT). A lifetime horizon was adopted in the analysis. A discount rate of 3.5% was applied to both costs and effects. The Italian National Healthcare Service (NHS) perspective was considered, therefore only healthcare direct costs (acquisition of main interventions and subsequent procedures; medications; monitoring and follow-up; adverse events). Model robustness was tested through sensitivity analyses.
    Results: Results of the base-case analysis showed that the total lifetime costs were higher in the iStent inject® + concurrent cataract surgery, compared with the cataract surgery alone group (€8368.51 vs. €7134.71 respectively). iStent inject® + concurrent cataract surgery was cost-effective vs. cataract surgery alone, with an incremental cost-effectiveness ratio of €13,037.01 per quality-adjusted life year (QALY) gained. Both one-way deterministic and probabilistic sensitivity analyses confirmed robustness of base-case results. The cost-effectiveness accessibility curve (CEAC) showed that iStent inject® + cataract surgery would have a 98% probability of being cost-effective, compared to cataract surgery alone, when the willingness to pay (WTP) is equal to €50,000 per QALY gained.
    Conclusions: The results of the cost-utility analysis confirm that iStent inject® + cataract surgery is a cost-effective option for the treatment of patients affected by mild-to-moderate POAG, compared with cataract surgery alone, when evaluated from the Italian NHS perspective.
    MeSH term(s) Cost-Benefit Analysis ; Glaucoma, Open-Angle/surgery ; Humans ; Intraocular Pressure ; Italy ; Stents
    Language English
    Publishing date 2021-08-17
    Publishing country England
    Document type Journal Article ; Randomized Controlled Trial
    ISSN 1472-6963
    ISSN (online) 1472-6963
    DOI 10.1186/s12913-021-06862-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Sorafenib maintenance after hematopoietic stem cell transplantation improves outcome of FLT3-ITD-mutated acute myeloid leukemia.

    Aydin, Semra / Passera, Roberto / Scaldaferri, Matilde / Dellacasa, Chiara Maria / Poggiu, Marco / Cattel, Francesco / Zallio, Francesco / Brunello, Lucia / Giaccone, Luisa / Dogliotti, Irene / Busca, Alessandro

    International journal of hematology

    2022  Volume 116, Issue 6, Page(s) 883–891

    Abstract: In a retrospective analysis, 21 acute myeloid leukemia patients receiving single-agent sorafenib maintenance therapy in complete remission (CR) after hematopoietic stem cell transplantation (HSCT) were compared with a control group of 22 patients without ...

    Abstract In a retrospective analysis, 21 acute myeloid leukemia patients receiving single-agent sorafenib maintenance therapy in complete remission (CR) after hematopoietic stem cell transplantation (HSCT) were compared with a control group of 22 patients without maintenance. Sorafenib was initiated a median of 3 months (IQR: 2.3-3.5) after allogeneic HSCT with a median daily dosage of 400 mg (range: 200-800) orally, and lasted a median of 11.3 months (IQR: 3.3-24.4). No significant increase in graft versus host disease or toxicity was observed. Adverse events were reversible with dose adjustment or temporary discontinuation in 19/19 cases. With a median follow-up of 34.7 months (IQR: 16.9-79.5), sorafenib maintenance significantly improved cumulative incidence of relapse (p = 0.028) as well as overall survival (OS) (p = 0.016), especially in patients undergoing allogeneic HSCT in CR1 (p < 0.001). In conclusion, sorafenib maintenance after allogeneic HSCT is safe and may improve cumulative incidence of relapse and OS in FLT3-ITD-mutated AML.
    MeSH term(s) Humans ; Sorafenib/therapeutic use ; Phenylurea Compounds/adverse effects ; Transplantation, Homologous ; Retrospective Studies ; Niacinamide/therapeutic use ; Hematopoietic Stem Cell Transplantation/adverse effects ; Leukemia, Myeloid, Acute/therapy ; Leukemia, Myeloid, Acute/drug therapy ; Recurrence ; fms-Like Tyrosine Kinase 3/genetics ; Mutation
    Chemical Substances Sorafenib (9ZOQ3TZI87) ; Phenylurea Compounds ; Niacinamide (25X51I8RD4) ; fms-Like Tyrosine Kinase 3 (EC 2.7.10.1) ; FLT3 protein, human (EC 2.7.10.1)
    Language English
    Publishing date 2022-08-09
    Publishing country Japan
    Document type Journal Article
    ZDB-ID 1076875-0
    ISSN 1865-3774 ; 0917-1258 ; 0925-5710
    ISSN (online) 1865-3774
    ISSN 0917-1258 ; 0925-5710
    DOI 10.1007/s12185-022-03427-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Ozone therapy in COVID-19: A narrative review.

    Cattel, Francesco / Giordano, Susanna / Bertiond, Cecilia / Lupia, Tommaso / Corcione, Silvia / Scaldaferri, Matilde / Angelone, Lorenzo / De Rosa, Francesco Giuseppe

    Virus research

    2020  Volume 291, Page(s) 198207

    Abstract: The main objective of this narrative review is to describe the available evidence on the possible antiviral activity of ozone in patients with COVID-19 and its therapeutic applicability through hospital protocols. Amongst different possible therapies for ...

    Abstract The main objective of this narrative review is to describe the available evidence on the possible antiviral activity of ozone in patients with COVID-19 and its therapeutic applicability through hospital protocols. Amongst different possible therapies for SARS-CoV-2 pneumonia, ozone therapy seems to have an immunological role because of the modulation of cytokines and interferons, including the induction of gamma interferon. Some data suggest the possible role of ozone therapy in SARS, either as a monotherapy or, more realistically, as an adjunct to standard treatment regimens; therefore, there is increasing interest in the role of ozone therapy in COVID-19 treatment The PubMed and Scopus databases and the Italian Scientific Society of Oxygen Ozone Therapy website were used to identify articles focused on ozone therapy. The search was limited to articles published from January 2011 to July 2020. Of 280 articles found on ozone therapy, 13 were selected and narratively reviewed. Ozone exerts antiviral activity through the inhibition of viral replication and direct inactivation of viruses. Ozone is an antiviral drug enhancer and is not an alternative to antiviral drugs. Combined treatment with involving ozone and antivirals demonstrated a reduction in inflammation and lung damage. The routes of ozone administration are direct intravenous, major autohaemotherapy and extravascular blood oxygenation-ozonation. Systemic ozone therapy seems useful in controlling inflammation, stimulating immunity and as antiviral activity and providing protection from acute coronary syndromes and ischaemia reperfusion damage, thus suggesting a new methodology of immune therapy. Systemic ozone therapy in combination with antivirals in COVID-19-positive patients may be justified, helpful and synergic.
    MeSH term(s) Antiviral Agents/therapeutic use ; COVID-19/drug therapy ; Humans ; Ozone/therapeutic use
    Chemical Substances Antiviral Agents ; Ozone (66H7ZZK23N)
    Keywords covid19
    Language English
    Publishing date 2020-10-25
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 605780-9
    ISSN 1872-7492 ; 0168-1702
    ISSN (online) 1872-7492
    ISSN 0168-1702
    DOI 10.1016/j.virusres.2020.198207
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Cost-utility analysis of trabecular micro-bypass stents (TBS) in patients with mild-to-moderate open-angle Glaucoma in Italy

    Antonio Maria Fea / Francesco Cattel / Stefano Gandolfi / Giorgio Buseghin / Gianluca Furneri / Ciro Costagliola

    BMC Health Services Research, Vol 21, Iss 1, Pp 1-

    2021  Volume 12

    Abstract: Abstract Background Glaucoma is a disease characterized by progressive damage of the optic nerve. Several therapeutic options are available to lower intraocular pressure (IOP). In primary open-angle glaucoma (POAG) patients with inadequate IOP control ( ... ...

    Abstract Abstract Background Glaucoma is a disease characterized by progressive damage of the optic nerve. Several therapeutic options are available to lower intraocular pressure (IOP). In primary open-angle glaucoma (POAG) patients with inadequate IOP control (or controlled with multiple medical therapies or for whom medical therapy is contraindicated), the implantation of micro-invasive glaucoma surgery devices (MIGS) and concomitant cataract surgery has proved to be more effective in reducing intraocular pressure (IOP), as compared to cataract surgery alone. The objective of this study was to assess the cost-effectiveness of iStent inject® device with concurrent cataract surgery vs. cataract surgery alone, in patients with mild-to-moderate POAG, adopting the Italian National Health Service (NHS) perspective. Methods Simulation of outcomes and costs was undertaken using a Markov model with 4 health states and one-month cycles, that is used to simulate the prognosis of these patients. Efficacy data were obtained from the randomized clinical trial (RCT). A lifetime horizon was adopted in the analysis. A discount rate of 3.5% was applied to both costs and effects. The Italian National Healthcare Service (NHS) perspective was considered, therefore only healthcare direct costs (acquisition of main interventions and subsequent procedures; medications; monitoring and follow-up; adverse events). Model robustness was tested through sensitivity analyses. Results Results of the base-case analysis showed that the total lifetime costs were higher in the iStent inject® + concurrent cataract surgery, compared with the cataract surgery alone group (€8368.51 vs. €7134.71 respectively). iStent inject® + concurrent cataract surgery was cost-effective vs. cataract surgery alone, with an incremental cost-effectiveness ratio of €13,037.01 per quality-adjusted life year (QALY) gained. Both one-way deterministic and probabilistic sensitivity analyses confirmed robustness of base-case results. The cost-effectiveness accessibility curve (CEAC) ...
    Keywords Cost-effectiveness ; Minimally invasive surgery ; glaucoma ; IOP reduction ; Trabecular bypass ; Public aspects of medicine ; RA1-1270
    Subject code 670
    Language English
    Publishing date 2021-08-01T00:00:00Z
    Publisher BMC
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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