Back to articles
Research & Diagnostics
ANSES
Antimicrobial resistance
Biodiversity
Ecotoxicity
Endocrine disruptors
Heavy Metals
Hormones
Marketing authorisation
Medication
Micropollutants
PCB
Pesticides
Pharmaceutical Industry
Pharmacy
Residues of drugs
SIMV
Ségolène Royal
Veterinarian
Veterinary medicine
Residues of Pharmaceuticals: An International Conference and a National Plan to Combat Micropollutants
V
Vetitude
09/12/2016
9 min read
0 comments
Share:
Originally expected in June, the second “National Micropollutants Plan” was officially launched on September 8. Ségolène Royal, the Minister of the Environment, made the announcement at the opening of the first international conference on the risks associated with pharmaceutical residues in the environment, organized in Paris by the National Academy of Pharmacy. Covering the period 2016–2021, this strategic plan aims to reduce pollutant emissions into water and preserve the quality of aquatic environments and biodiversity. It has three objectives: to reduce emissions at the source, to consolidate knowledge in order to tailor response efforts, and to identify and prioritize the substances that require action.
Medications, heavy metals, PCBs, hormones, etc.: there are countless substances capable of having toxicity in natural environments, even at very low concentrations. Furthermore, the cost of water pollution caused by micropollutants is high: for example, removing 1 kg of pesticides from water to produce drinking water costs between €60,000 and €200,000.
According to the Court of Auditors, the cost of remedial treatment per cubic meter of water is, moreover, 2.5 times higher than that of preventive treatment
. In light of these findings, the Ministries of Ecology, Health, and Agriculture have decided to develop, by 2021, initiatives aimed at reducing micropollutants at the source.
Over the past six to eight years, three action plans to combat pollution of aquatic environments by these micropollutants have been implemented in France. Now that those plans have come to an end, the new “Micropollutants Plan to Preserve Water Quality and Biodiversity” is taking over. Building on the findings of the previous plans, it is structured around 3 objectives (reduce, understand, prioritize), 14 levers, and 39 actions (see below)
.
Currently, while the presence of pharmaceutical residues in water is well established, the range of molecules present, the level of exposure, and the effects on fauna, flora, and human health remain largely unknown. In particular, the effects of interactions with other pollutants have not been assessed. Regarding antimicrobial resistance, there is also a lack of knowledge about the numerous mechanisms by which bacteria in municipal or hospital wastewater acquire resistance.
These residues originate from the pharmaceutical industry, from medications and diagnostic products disposed of with household waste, from urban or hospital wastewater, as well as from industrial livestock farming and land-applied sludge. While the impacts on wildlife and the environment are cause for concern (proliferation of antibiotic-resistant bacteria in certain waterways, disrupted fish reproduction due to residues of endocrine disruptors, etc.), the concentrations found in drinking water—at least in developed countries—are fortunately much lower. As for food, uncertainties remain, again due to a lack of data.
At the international conference on September 8 and 9, some 250 experts gathered in Paris to discuss research challenges related to the issue of these pharmaceutical residues in the environment and to take stock of the knowledge gained over the past decade. In her opening remarks, Ségolène Royal emphasized the importance of data sharing to better understand the risks and the level of exposure to human and veterinary drug residues in water: “To date, no reliable database exists on the physicochemical, toxicological, and ecotoxicological properties of drugs. Centralizing this data would make it possible to more effectively prioritize molecules based on their risk of ending up in water or exceeding threshold levels.”
The minister also announced, in the preamble to the second action plan, that she had referred the matter to the French Agency for Food, Environmental and Occupational Health & Safety (ANSES) in order to “objectively assess the mechanisms involved in the development of antimicrobial resistance in the environment and define new risk-reduction measures regarding the interface between human medicine, veterinary medicine, and the environment.”
In addition, her ministry will fund “a systematic review intended to take stock of current knowledge on the contamination of the environment with antibiotics, biocides, and resistant bacteria.”
With regard to reducing or eliminating emissions, one of the identified levers is to address marketing authorizations (MA) for drugs, which now include new procedures requiring the assessment of ecotoxicity.
Monitoring of emerging compounds, relevant substances, pollutants specific to ecological status, and hazardous substances will provide the necessary information before granting or revising a marketing authorisation.
A steering committee for the new micropollutants plan will meet at least once a year to review the progress of the actions. It will be chaired by the Ministries of Ecology, Health, and Agriculture. In addition, measures addressing pharmaceutical residues may be expanded following the development of a strategy by the European Commission to combat this form of water pollution.
* http://www.developpement-durable.gouv.fr/IMG/pdf/Plan_micropolluants_2016-_2021.pdf
Commentaires
No comments yet.
Sign in to comment