Evidence map›Paper›PMID 29609613›Full record

ArticleBMC health services research2018

Use of analgesics in France, following dextropropoxyphene withdrawal.

E Van Ganse, M Belhassen, M Ginoux, E Chrétien, C Cornu, C Ecoffey, F Aubrun

Abstract read
In one paragraph

Article in BMC health services research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Observational
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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

E Van GanseHESPER 7425, Health Services and Performance Research, University Claude Bernard Lyon 1, Lyon, France. eric.van-ganse@univ-lyon1.fr.
M BelhassenHESPER 7425, Health Services and Performance Research, University Claude Bernard Lyon 1, Lyon, France.
M GinouxHESPER 7425, Health Services and Performance Research, University Claude Bernard Lyon 1, Lyon, France.
E ChrétienDepartment of Anesthesiology and Critical Care, Croix Rousse University Hospital, Claude Bernard Lyon 1 University, Lyon, France.
C CornuUMR 5558, Laboratoire de Biométrie et Biologie Evolutive, Claude Bernard University, CNRS, Lyon, France.
C EcoffeyDepartment of Anaesthesiology and Critical Care, Ponchaillou University Hospital, CIC Inserm, Rennes, France.
F AubrunHESPER 7425, Health Services and Performance Research, University Claude Bernard Lyon 1, Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn 2009, the European Medicines Agency recommended withdrawal of dextropropoxyphene (DXP); in March 2011 it was withdrawn from the market in France. Up until that time the combination dextropropoxyphene-paracetamol (DXP/PC) was widely used for analgesia. At withdrawal, French regulators recommended that DXP/PC be replaced by other step 2 analgesics, i.e. tramadol, codeine, or opium-containing drugs, or by PC for a weak level of pain. To investigate prescribing behaviours after DXP/PC withdrawal, dispensations of analgesics before and after withdrawal were analysed.

methodsAggregated dispensation data of analgesics prescribed between January 2009 and December 2012 in the Rhône-Alpes region were obtained from the general health insurance claims data; changes in analgesic dispensation over time were analysed with the ATC/DDD methodology. Pre (Jan-June 2009) and post-withdrawal (Jan-June 2012) changes of DDDs where computed for each analgesic step.

resultsThe dispensations of DXP/PC experienced a two-step decrease until 2011. Over the withdrawal period 2009-2012, there was a 14% decrease in the overall use of analgesic (from 109 to 94 DDDs), while the use of step 2 analgesics declined by 46% (- 22 DDDs, from 47 to 25 DDDs). This latter decline included a cessation of use of DXP/PC (29 DDDs in 2009) that were only in part (+ 7 DDDs, from 18 to 25 DDDs) compensated by increased use of codeine, tramadol and opium, in monotherapy or combined with PC. For step 1 analgesics, use increased with 9%, mostly PC (+ 8 DDDs, from 31 to 39 DDDs). Step 3 analgesics dispensations remained largely unchanged over this period (around 3 DDDs).

conclusionsIn the Rhône-Alpes region, DXP/PC withdrawal was accompanied in part by an increased use of same level analgesics, and in part by an increased use of PC in monotherapy. The extent of DXP/PC use before withdrawal, and the increased use of PC after DXP withdrawal, underline the complexity of pain management.

Indexed as

AcetaminophenAnalgesicsAnalgesics, OpioidCodeineDextropropoxypheneDrug CombinationsDrug PrescriptionsFranceHumansPainPain ManagementSafety-Based Drug WithdrawalsTramadolAcetaminophenacetaminophen, dextropropoxyphene, drug combinationAnalgesicsAnalgesics, OpioidCodeineDextropropoxypheneDrug CombinationsTramadolAnalgesicsDrug withdrawalPain managementReal-life use

Identifiers

PMID29609613
PMCPMC5880096

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