Evidence map›Paper›PMID 31217000›Full record

ArticleBMC health services research2019

Human health benefit and burden of the schizophrenia health care pathway in Belgium: paliperidone palmitate long-acting injections.

Sam Debaveye, Delphine De Smedt, Bert Heirman, Shane Kavanagh, Jo Dewulf

Abstract read
In one paragraph

Article in BMC health services research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Points to consider for incorporating climate impacts into health economic evaluation.The European journal of health economics : HEPAC : health economics in prevention and care · 2026
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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

5 authors.

Sam DebaveyeResearch Group Environmental Organic Chemistry and Technology (EnVOC), Faculty of Bioscience Engineering, Ghent University, Campus Coupure, Coupure Links 653, B-9000, Ghent, Belgium. Sam.Debaveye@UGent.be.ORCID http://orcid.org/0000-0001-6731-3536
Delphine De SmedtDepartment of Public Health, Ghent University, Campus UZ, De Pintelaan 185, B-9000, Ghent, Belgium.
Bert HeirmanJohnson & Johnson EHS&S, Janssen Pharmaceutica NV, Turnhoutseweg 30, B-2340, Beerse, Belgium.
Shane KavanaghHealth Economics, Janssen Pharmaceutica NV, Turnhoutseweg 30, B-2340, Beerse, Belgium.
Jo DewulfResearch Group Environmental Organic Chemistry and Technology (EnVOC), Faculty of Bioscience Engineering, Ghent University, Campus Coupure, Coupure Links 653, B-9000, Ghent, Belgium.

Funding

Flemish Innovation and Entrepreneurship (VLAIO) Baekeland grant no. 140249Janssen Pharmaceutica Research jointly funded with VLAIO under same grant no. 140249
6 · The paper itself

Abstract

backgroundEnvironmental impact assessments of pharmaceuticals typically consider only a part of the pharmaceutical supply chain, e.g. tablet formulation. While the environmental impact can be expressed in environmental Human Health burden due to resource use and emissions, the Human Health benefit of the pharmaceutical treatment of patients is currently not simultaneously taken into account. The study aims include a cradle-to-grave assessment of all Human Health impacts of the production, administration and disposal of two antipsychotics for the treatment of schizophrenia. This is complemented with the environmental impact of health care providers such as hospitals. The aim is to holistically quantify to what extent the environmental Human Health burden compares to the Human Health benefit associated with the treatment.

methodsWe applied an overall framework which included Life Cycle Assessment to model the environmental Human Health impacts of the pharmaceutical supply chain, administration and disposal of the drug and health care providers. To model the patient benefit, this was complemented with a Markov model with a 1-year time horizon. Three patient groups were modeled: medicine coverage of paliperidone palmitate for either one month (PP1M) or three months (PP3M) at a time, and compared to Treatment Interruption (TI) as a control group. Outcomes were quantified using Years of Life Lost (YLL), Years Lived with Disability (YLD) and Disability-Adjusted Life Years (DALY).

resultsThe main environmental impacts were visits to the psychiatrist and psychiatric hospitals. The pharmaceutical supply chain had a limited impact. For 1000 patients for 1 year, PP1M and PP3M respectively avoided 0.38 and 0.49 environmental DALYs compared to TI. PP1M and PP3M further avoided 45.60 and 57.87 YLL and 23.31 and 29.91 YLD compared to TI. The main outcome was the sum of environmental DALYs, YLL and YLD, in which PP1M and PP3M respectively avoided 69.29 and 88.26 DALYs. Alternative analysis of Quality-Adjusted Life Years confirmed the results.

conclusionsThe overall environmental burden was lower for PP1M and PP3M treatment than Treatment Interruption because patients are kept more stable, which reduces the environmental burden due to hospitals. Moreover, the Human Health burden was outweighed by the Human Health benefit.

Indexed as

AdultAntipsychotic AgentsBelgiumDelayed-Action PreparationsFemaleHealth Services ResearchHumansInjectionsMaleMiddle AgedPaliperidone PalmitatePolicy MakingRisk AssessmentSchizophreniaYoung AdultAntipsychotic AgentsDelayed-Action PreparationsPaliperidone PalmitateEnvironmental sustainabilityLife cycle assessmentPaliperidone palmitate.Pharmaceutical science

Identifiers

PMID31217000
PMCPMC6585029

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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.