Evidence map›Paper›PMID 31797311›Full record

ArticleClinical drug investigation2020

PCSK9 Inhibitors' New Users: Analysis of Prescription Patterns and Patients' Characteristics from an Italian Real-world Study.

Carlo Piccinni, Ippazio Cosimo Antonazzo, Aldo P Maggioni, Antonella Pedrini, Silvia Calabria, Giulia Ronconi, Letizia Dondi, Nello Martini, Giuseppe Roberto, Tiziana Sampietro and 7 more

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Article in Clinical drug investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.8field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 35 citations in OpenAlex.

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  7. Retrospective real-world analysis of adherence and persistence to lipid-lowering therapy in Germany.Clinical research in cardiology : official journal of the German Cardiac Society · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 1 country.

Carlo PiccinniFondazione ReS (Ricerca e Salute)-Research and Health Foundation, Via Magnanelli 2, Casalecchio di Reno, 40033, Bologna, Italy. piccinni@fondazioneres.it.ORCID http://orcid.org/0000-0002-8648-8961
Ippazio Cosimo AntonazzoEpidemiology Unit, Regional Agency for Healthcare Services of Tuscany, Florence, Italy.
Aldo P MaggioniFondazione ReS (Ricerca e Salute)-Research and Health Foundation, Via Magnanelli 2, Casalecchio di Reno, 40033, Bologna, Italy.
Antonella PedriniFondazione ReS (Ricerca e Salute)-Research and Health Foundation, Via Magnanelli 2, Casalecchio di Reno, 40033, Bologna, Italy.
Silvia CalabriaFondazione ReS (Ricerca e Salute)-Research and Health Foundation, Via Magnanelli 2, Casalecchio di Reno, 40033, Bologna, Italy.
Giulia RonconiFondazione ReS (Ricerca e Salute)-Research and Health Foundation, Via Magnanelli 2, Casalecchio di Reno, 40033, Bologna, Italy.
Letizia DondiFondazione ReS (Ricerca e Salute)-Research and Health Foundation, Via Magnanelli 2, Casalecchio di Reno, 40033, Bologna, Italy.
Nello MartiniFondazione ReS (Ricerca e Salute)-Research and Health Foundation, Via Magnanelli 2, Casalecchio di Reno, 40033, Bologna, Italy.
Giuseppe RobertoEpidemiology Unit, Regional Agency for Healthcare Services of Tuscany, Florence, Italy.
Tiziana SampietroLipoapheresis Unit, Reference Centre for Diagnosis and Treatment of Inherited Dyslipidaemias, Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
Francesco SbranaLipoapheresis Unit, Reference Centre for Diagnosis and Treatment of Inherited Dyslipidaemias, Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
Beatrice Dal PinoLipoapheresis Unit, Reference Centre for Diagnosis and Treatment of Inherited Dyslipidaemias, Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
Federico BigazziLipoapheresis Unit, Reference Centre for Diagnosis and Treatment of Inherited Dyslipidaemias, Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
Giuseppa Lo SurdoHospital Pharmacy, Fondazione Toscana Gabriele Monasterio, Massa, Italy.
Elisabetta VolpiHospital Pharmacy, Fondazione Toscana Gabriele Monasterio, Massa, Italy.
Stefania BiaginiHospital Pharmacy, Fondazione Toscana Gabriele Monasterio, Massa, Italy.
Rosa GiniEpidemiology Unit, Regional Agency for Healthcare Services of Tuscany, Florence, Italy.
Fondazione Toscana Gabriele Monasterio · ITAgenzia Regionale di Sanità della Toscana · ITAssociazione Nazionale Medici Cardiologi Ospedalieri · ITFondazione Roma · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveCardiovascular (CV) diseases represent a major cause of death and severe medical condition worldwide. Different therapeutic options are available to control low-density lipoprotein cholesterol (LDL-C) level in order to prevent CV events. In recent years, two new drugs were approved for patients who are unable to reduce circulating LDL-C with the current therapies: evolocumab and alirocumab (proprotein convertase subtilisin/kexin type nine [PCSK9] inhibitors). This study was aimed to characterise patients who started treatment with PCSK9 inhibitors in the Tuscany region of Italy during the first year of public healthcare service reimbursement and to describe the pattern of PCSK9 inhibitor use in the first 6 months of treatment.

methodsPatients on PCSK9 inhibitor treatment in Tuscany (3.7 million inhabitants) from 07/2017 to 06/2018 were selected from regional healthcare administrative databases. Concomitant use of lipid-lowering therapies (LLTs), adherence and persistence during the 6 months preceding the first PCSK9 inhibitor dispensing, as well as comorbidities since 1996, were described. In the first 6 months of PCSK9 inhibitor treatment, adherence, persistence and concomitant LLTs were assessed.

resultsThere were 269 (176 evolocumab, 93 alirocumab) new users of PCSK9 inhibitors. Patients (mean age of 59.1 years) were mainly male (71.0%) in secondary prevention (70.2%) and affected by familial hypercholesterolaemia (53.5%). Sixty-six patients (24.5%) had diabetes mellitus and 12 (4.5%) chronic renal failure. In the 6 months prior to the first PCSK9 inhibitor administration, 61.3% of patients received at least one prescription of ezetimibe or high-intensity statins and 45.7% were persistent to these drugs. During follow-up, 79.9% of patients were adherent to PCSK9 inhibitor and 73.3% were persistent.

conclusionsDuring the first year of availability, the rate of prescription of PCSK9 inhibitors appears below expectations. Patients were mainly in secondary prevention and had been slightly persistent to previous LLTs. During follow-up, the PCSK9 inhibitor monotherapy showed high levels of adherence and persistence. This real-world study sets the stage for future longer-term investigations useful to improve our knowledge on the appropriateness, drug access and public healthcare sustainability of PCSK9 inhibitors.

Indexed as

PCSK9 InhibitorsAdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedCardiovascular DiseasesCholesterol, LDLDrug PrescriptionsEzetimibeFemaleHumansHydroxymethylglutaryl-CoA Reductase InhibitorsMaleMiddle AgedSecondary PreventionalirocumabAntibodies, Monoclonal, HumanizedCholesterol, LDLevolocumabEzetimibeHydroxymethylglutaryl-CoA Reductase InhibitorsPCSK9 Inhibitors

Identifiers

PMID31797311
OpenAlexW2992678675

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.