FIGURE 3
LETTER TO MANUFACTURERS
Dear Product Manager:
As a result of documented incidents of anaphylactic reactions by patients and staff from exposure to natural rubber latex products, the
Administration of (________) has directed Materials Management to determine the natural rubber latex content of all items
in the hospital inventory. We currently stock the following product, purchased from your company, as a hospital inventory item.
PRODUCT DESCRIPTION: _____________
MFG. PRODUCT NO: _________________
CHW ITEM NUMBER:_________________
Please complete the section below and retum this letter to me at the above address.
_____ The above product does not contain any natural rubber latex in its components or ingredients.
_____ The above product does contain natural rubber latex in its components and/or ingredients.
Please identify the natural rubber latex components and/or specify the latex ingredients.
____________________________________________________________________
____________________________________________________________________
On behalf of the manufacturer (please fill in):________________________________, the above
section is complete and accurate to the best of my knowledge.
Name__________ Title__________
Signature__________ Date__________
RETURN COMPLETED LETTER NO LATER THAN ______________. FAILURE TO RESPOND MAY
RESULT IN THE INVESTIGATION OF DOCUMENTED NON-LATEX ALTERNATIVES TO YOUR PRODUCT.
Sincerely,
Materials Management
FIGURE 4
RECOMMENDATIONS FOR CARE OF THE LATEX-SENSITIZED PATIENT
- The patient should wear a medical bracelet alerting personnel
to the risk of latex allergy.
- The medical chart, room, and bed is labeled to avoid latex
products being inadvertently brought or stored in the room.
- Clear notation in the medical record of how a diagnosis or
suspected diagnosis was made.
- Only non-latex exam gloves be used in the room where a
latex-sensitive patient is cared for (e.g., on another patient)
whether they actually contact the patient or not.
- Prepackaged kits and trays that contain latex products should
not be used. Packages may be closed using a latex glue. Keep
this in mind when opening the package.
- Three-way stopcocks are placed in intravenous lines for the
administration of medications.
- Rubber medication stoppers should not be used. Remove the
stopper with a can opener before drawing up the medication.
- Intravenous tubing without latex injection ports should be
used. If this is not possible, tape over the ports and do not use.
- Patients with suspected latex sensitization are referred to their
physician for evaluation.
- Patients who have developed systemic symptoms or
anaphylaxis should carry an injectable epinephrine emergency
medication at all times.
- Patients in a high risk group (e.g., genitourinary tract anomaly)
who have not exhibited symptoms of latex allergy should have
limited exposure to latex products when possible.