Medical warnings warn the provider of any known dangers relating to the specific individual and the administration of therapeutic medicines (eg, allergies, drug sensitivities, or adverse medical reactions). Warnings are categorised as ‘warnings’ or ‘dangers’. Doctors submit an incident, such as an allergic reaction, as a warning. The Centre for Adverse Reactions Monitoring can review and upgrade this warning to a danger if it could be potentially life-threatening.
Medical alerts indicate significant medical conditions, such as renal failure requiring dialysis, which are likely to have an impact on care decisions.
Like the NHI, the MWS contains information of operational-level significance, and the responsibility for maintaining the content of the MWS rests with health and disability support services.
The MWS enables important data from different clinical information systems to be available to these services where and when it could be important.
The purpose of the MWS is to warn health providers of any known risk factors that may be important when making clinical decisions about individual patient care.
Each medical warning consists of:
Types of warnings in the Medical Warning System are:
Doctors in hospitals have access to MWS, to review any warnings and alerts when they are treating patients. They can also create warnings for their patients.
CARM assess reports of adverse reactions and following clinical review create warnings on MWS.
Work is underway to give GPs access to MWS medication, food and environmental allergies. Currently this is not widely available primary care.