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Welcome to the international HTA database

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Year Source Title
2016     Technology Assessment Unit of the McGill University Health Centre (MUHC) A mini-health technology assessment of Linear and Radial Endobronchial Ultrasound (EBUS) and Electromagnetic Navigation Bronchoscopy (ENB) in the diagnosis and staging of lung cancer in adults
2016     Technology Assessment Unit of the McGill University Health Centre (MUHC) Cardiac resynchronization therapy in heart failure
2016     Technology Assessment Unit of the McGill University Health Centre (MUHC) Use of biventricular pacing in atrioventricular heart block
2017     Technology Assessment Unit of the McGill University Health Centre (MUHC) Use of extracorporeal membrane oxygenation for cardiac life support in adult subjects
2011     Technology Assessment Unit of the McGill University Health Centre (MUHC) Fiducial markers for improving treatment margins in radiotherapy for prostate cancer
2011     Technology Assessment Unit of the McGill University Health Centre (MUHC) Use of the VerifyNow point of care test to detect nonresponsiveness to clopidogrel and aspirin
2010     Technology Assessment Unit of the McGill University Health Centre (MUHC) Efficacy and cost-effectiveness of a gentamicin-loaded collagen sponge as an adjuvant antibiotic prophylaxis for colorectal surgery
2010     Technology Assessment Unit of the McGill University Health Centre (MUHC) Efficacy, safety and cost of ultrafiltration for the management of acute decompensated heart failure.
2010     Technology Assessment Unit of the McGill University Health Centre (MUHC) Negative Pressure Wound Therapy (NPWT) Update to Report 19
2005     Technology Assessment Unit of the McGill University Health Centre (MUHC) The use of probiotics in the prevention and treatment of clostridium difficile diarrhea
2014     Technology Assessment Unit of the McGill University Health Centre (MUHC) Islet transplantation in patients with Type 1 Diabetes Mellitus
2014     Technology Assessment Unit of the McGill University Health Centre (MUHC) Excimer laser atherectomy for uncrossable coronary lesions and improperly deployed coronary stents
2003     Technology Assessment Unit of the McGill University Health Centre (MUHC) Use of the implantable cardiac defibrillator (ICD) at the McGill University Health Centre (MUHC)
2003     Technology Assessment Unit of the McGill University Health Centre (MUHC) The use of self-expanding metallic stents in the palliation of dysphagia in patients with malignant esophageal strictures
2003     Technology Assessment Unit of the McGill University Health Centre (MUHC) An evaluation of drug eluting (coated) stents for percutaneous coronary interventions: what should their role be at the McGill University Health Centre (MUHC)?
2007     Technology Assessment Unit of the McGill University Health Centre (MUHC) The use of image-free computer-assisted systems in total knee replacement surgeries
2012     Technology Assessment Unit of the McGill University Health Centre (MUHC) Evaluation of acellular dermal matrix for breast reconstruction: an update
2007     Technology Assessment Unit of the McGill University Health Centre (MUHC) Drotrecogin alfa (activated) in severe sepsis
2012     Technology Assessment Unit of the McGill University Health Centre (MUHC) The hybrid operating room. Should one be available for cardiovascular-thoracic procedures in the MUHC? A brief report
2012     Technology Assessment Unit of the McGill University Health Centre (MUHC) Single-dose intraoperative radiotherapy using Intrabeam® for early-stage breast cancer: a health technology assessment
2007     Technology Assessment Unit of the McGill University Health Centre (MUHC) Pulsatile machine perfusion compared to cold storage in kidney preservation
2005     Technology Assessment Unit of the McGill University Health Centre (MUHC) Vacuum-assisted wound closure therapy (V.A.C (R))
2005     Technology Assessment Unit of the McGill University Health Centre (MUHC) Intraoperative neurophysiological monitoring during spinal surgery
2005     Technology Assessment Unit of the McGill University Health Centre (MUHC) Cerebral microdialysis as a tool for neuromonitoring following traumatic brain injury
2005     Technology Assessment Unit of the McGill University Health Centre (MUHC) Botulinum toxin A for the treatment of refractory chronic anal fissures and internal anal sphincter achalasia in pediatric patients
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Amikacin (Mycobacterium avium complex pulmonary infections)]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Atidarsagen autotemcel (metachromatic leukodystrophy with biallelic mutation in the ARSA gene)]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Autologous anti-CD19-transduced CD3+ cells (mantle cell lymphoma, pretreated patients)]
2021     The Federal Joint Committee (G-BA) Pharamceutical Directive/Annex XII: Avapritinib (gastrointestinal stromal tumours)
2019     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Axicabtagene ciloleucel (PMBCL)]
2020     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Bedaquiline (new therapeutic indication: multi-drug-resistant pulmonary tuberculosis, 12 to < 18 years)]
2023     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Birch Bark Extract (treatment of wounds associated with epidermolysis bullosa (6 months and older))
2023     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Efgartigimod alfa (Myasthenia Gravis, AChR-antibody+)
2021     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Cabozantinib (reassessment after the deadline: thyroid carcinoma)
2023     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Fenfluramine (new therapeutic indication: Lennox-Gastaut syndrome, add-on therapy, ≥ 2 years)
2022     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Voxelotor (haemolytic anaemia in sickle cell disease, monotherapy or combination with hydroxycarbamide, ≥ 12 years)
2022     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Avapritinib (new therapeutic indication: systemic mastocytosis, after at least 1 prior therapy)
2022     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Tebentafusp (uveal melanoma, HLA-A*02:01-positive)
2022     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Glucarpidase (reduction of toxic plasma methotrexate concentrations; aged 28 days and older)
2022     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Idebenone (reassessment after the deadline: Leber's Hereditary Optic Neuropathy)
2022     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Voretigene Neparvovec (reassessment after the deadline: inherited retinal dystrophy)
2022     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Somatrogon (growth disturbance due to growth hormone deficiency, ≥ 3 to < 18 years
2021     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Bedaquiline (new therapeutic indication: pulmonary multidrug-resistant tuberculosis, 5 to 11 years)
2019     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Bedaquiline (assessment of an orphan drug after exceeding the turnover limit of €1 million)
2021     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Belantamab mafodotin (multiple myeloma, at least 4 prior therapies, monotherapy)
2020     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Betibeglogene autotemcel (β-thalassaemia) (treatment costs)]
2021     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Benefit assessment of medicinal products with new active ingredients according to section 35a SGB V: blinatumomab (new therapeutic indication: B-precursor acute lymphoblastic leukaemia, relapsed or refractory, Ph+ CD19+)
2018     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Blinatumomab (new therapeutic indication: acute lymphatic leukaemia, paediatric patients aged 1 year or older)
2019     The Federal Joint Committee (G-BA) Pharmaceutical Directive (AM-RL): Annex XII – Benefit assessment of medicinal products with new active ingredients according to section 35a SGB V brentuximab vedotin (new therapeutic indication: Hodgkin lymphoma, first line)
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Bulevirtide (chronic hepatitis delta virus (HDV) infection)]
2020     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Burosumab (reassessment after the deadline: hypophosphataemia)]
2020     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Burosumab (new therapeutic indication: X-linked hypophosphataemia, ≥ 18 years)
2020     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Cannabidiol - reassessment after expiry of the deadline (Dravet-Syndrome, ≥ 2 years, combination with clobazam)
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Afamelanotide (Reassessment after the deadline: Phototoxicity in erythropoietic protoporphyria (EPP))]
2020     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Cannabidiol - reassessment after expiry of the deadline (Lennox-Gastaut-Syndrome, ≥ 2 years, combination with clobazam)
2019     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Caplacizumab (New Therapeutic Indication: Acquired Thrombotic Thrombocytopenic Purpura, 12 to < 18 Years)
2021     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Crizanlizumab (repeal of the resolution of 20 May 2021)
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Fenfluramine (Dravet syndrome, ≥ 2 years)]
2020     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Gilteritinib (Relapsed or Refractory Acute Myeloid Leukaemia with an FLT3 Mutation)
2020     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Givosiran (acute hepatic porphyria, ≥ 12 years)]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Glasdegib (acute myeloid leukaemia (AML), combination with cytarabine (LDAC))]
2019     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Glycerol phenylbutyrate (New Therapeutic Indication: Urea cycle disorders in infants aged 0 to < 2 months)]
2016     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Idebenone]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Imlifidase (desensitisation in kidney transplantation)]
2019     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Axicabtagene ciloleucel]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Luspatercept (β-thalassaemia)]
2019     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Mexiletine]
2023     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Asciminib (chronic myeloid leukaemia, Ph+, after ≥ 2 prior therapies)
2023     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Brexucabtagen Autoleucel (new therapeutic indication: relapsed or refractory B-cell precursor acute lymphoblastic leukaemia, 26 years of age and above)
2019     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Pegvaliase]
2020     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Tisagenlecleucel (reassessment after expiry: diffuse large B-cell lymphoma)]
2020     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Volanesorsen]
2019     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Voretigene Neparvovec
2022     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Pegcetacoplan (paroxysmal nocturnal haemoglobinuria, pretreated patients)
2023     The Federal Joint Committee (G-BA) Pharmaceutical Directive/Annex XII: Eladocagene exuparvovec (Aromatic-L-amino acid decarboxylase (AADC) deficiency, ≥ 18 months)
2013     The HTA Center of the Stockholm County Council/Gotland Cyanoacrylate and postoperative infections
2013     The HTA Center of the Stockholm County Council/Gotland Risks associated with planned home delivery for nulliparous women
2014     The HTA Center of the Stockholm County Council/Gotland [Wound infections after surgery-effect of triclosan-coated sutures]
2014     The HTA Center of the Stockholm County Council/Gotland [Superficial wound infections after colorectal surgery and appendectomy-favourable effect of Alexis wound edge protector]
2013     The HTA Center of the Stockholm County Council/Gotland MitraClip in patients with severe mitral insufficiency
2013     The HTA Center of the Stockholm County Council/Gotland Monitoring donor specific HLA-antibodies developed after kidney transplantation (de novo DSA)
2013     The HTA Center of the Stockholm County Council/Gotland Fetal monitoring with computerized ST analysis during labor: a systematic review and meta-analysis.
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) Package advice ravulizumab (Ultomiris®) for the treatment of PNH and aHUS
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) GVS advice tirbanibulin (Klisyri®) for the treatment of adults with actinic keratosis
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) Package advice venetoclax (Venclyxto®)
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) GVS assessment ponesimod (Ponvory®) for the treatment of relapsing forms of multiple sclerosis (RMS)
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) Package advice cemiplimab (Libtayo®) for the treatment of non-small cell lung carcinoma (NSCLC)
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) GVS assessment empagliflozin (Jardiance®) for the treatment of adults with chronic heart failure
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) GVS review levomepromazine (Nozinan®) for palliative sedation in a home situation
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) Extension of further conditions for SGLT2 inhibitors following recent GVS advice (22 June 2021)
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) GVS advice CGRP inhibitors erenumab, fremanezumab, galcanezumab (Aimovig®, AJOVY®, Emgality®) for the treatment of patients with episodic and chronic migraine
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) GVS advice roxadustat (Evrenzo®) for the treatment of symptomatic anaemia in chronic kidney damage
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) GVS advice drospirenon-estetrol (Drovelis®)
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) Follow-up advice on conditional inclusion of larotrectinib (Vitrakvi®)
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) Follow-up advice on conditional inclusion of entrectinib (Rozlytrek®)
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) Package advice ipilimumab (Yervoy®) in combination with nivolumab (Opdivo®)
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) GVS advice on the reassessment of tafamidis (Vyndaqel®)
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) Advice on the reassessment of axicabtagene ciloleucel (Yescarta®)
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) GVS advice on ferrimaltol (Feraccru®) for treating iron deficiency
2021     The National Health Care Institute (ZIN, Zorginstituut Nederland) GVS advice on subcutaneous buprenorphine (Buvidal®)