Latex Allergy Treatment & Management

Updated: Jan 08, 2016
  • Author: Amy J Behrman, MD, FACOEM, FACP; Chief Editor: Erik D Schraga, MD  more...
  • Print

Prehospital Care

Prehospital providers should be aware of the risk of latex allergy in patients and providers.

Search for and read MedicAlert-type bracelets.

Note the patient's history of relevant allergies to medical devices or fruits.

To rule out latex allergy that could worsen with further medical exposure, review the patient's history of activities/exposures immediately preceding any systemic allergic reaction.

Use powder-free latex gloves or, ideally, high-quality nonlatex gloves to minimize risk to patients and providers in all circumstances. Latex-free resuscitation and intravenous (IV) access equipment should be available for high-risk patients. Do not give medication from rubber-topped multidose vials or through latex IV ports in latex-allergic patients.


Emergency Department Care

Patients with known or suspected latex allergy who seek care for unrelated medical conditions or injuries must be kept within a latex-safe environment to prevent serious complications. This includes all patients with spina bifida.

Patients presenting with frank symptoms of type I latex allergy are treated as any other patients with systemic allergic reactions, except they must be protected from further latex contact to avoid clinical deterioration. Many EDs, hospitals, and medical offices represent very high-risk environments for latex-sensitive patients, particularly if powdered latex gloves are still in use.

  • Latex-free resuscitation equipment must be available. This frequently is accomplished with a mobile, latex-free cart carrying non-latex intubation and ventilation equipment, IV tubing, syringes, tourniquets, electrode pads, gloves, masks, and medication vials.

  • Routine care of high-risk patients should use non-latex supplies. Major reactions in sensitized patients have been precipitated with pelvic and rectal exams using latex gloves, urinary catheterization with latex catheters, IV medication given through latex ports, and inhalation of aerosolized latex glove powder.

  • Consultants must be aware of the need to completely avoid latex exposure to the patient during examinations and procedures.

  • Patients needing studies in other hospital areas, such as radiology, must be transported without risking latex exposure.

  • Identification of latex versus non-latex medical devices traditionally has required laborious contacts with individual manufacturers. Since 1999, the US Food and Drug Administration has required all manufacturers to apply warning labels to medical devices containing natural rubber latex. [33] This regulation has helped to facilitate safe care of patients who are allergic to latex. In addition, medical device manufacturers have developed many latex-free alternatives for routine care and invasive procedures. However, providers should be aware that package labeling for latex content may not be clear, and that latex-containing medications and devices can be mistaken for latex-free products in busy clinical settings.



Consultants must be aware of the need to scrupulously avoid exposing the patient to latex during exams and procedures.