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U.S. Department of Health and Human Services

Medical Devices

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FDA Safety Alert: Entrapment Hazards with Hospital Bed Side Rails

This is an archived document and is no longer current information.

August 23, 1995

TO:Biomedical/Clinical Engineers
Directors of Nursing
Home Healthcare Agencies
Hospices
Hospital Administrators
Nursing Associations
Nursing Homes
Risk Managers

This Safety Alert concerns entrapment hazards associated with the use of hospital bed side rails in a small, identifiable patient population, and recommends certain actions to prevent such hazards. The Alert is not specific to any manufacturer or product; it is part of a cooperative effort between FDA, the healthcare industry, and manufacturers to resolve the problem. Currently, no universal standards exist for design of hospital bed side rails.

Since January 1990, FDA has received 102 reports of head and body entrapment incidents involving hospital bed side rails. The 68 deaths, 22 injuries, and 12 entrapments without injury occurred in hospitals, long-term care facilities, and private homes. The U.S. Consumer Product Safety Commission, the United Kingdom Department of Health, and the Canadian Health Protection Branch have also received similar reports of entrapment.(1,2,3) Although the number of reported incidents is small relative to the large number of patients who use hospital beds, we believe appropriate precautions can reduce further incidents.

All reported entrapments occurred in one of the following ways (numbered 1-4 in the diagram below):

  1. through the bars of an individual side rail;
  2. through the space between split side rails;
  3. between the side rail and mattress; or
  4. between the headboard or footboard, side rail, and mattress.

 

Entrapment Points on Enclosed Bed System Side Rails

All deaths involved entrapment of the head, neck, or thorax, while most injuries involved fractures, cuts, and abrasions to the extremities. Although an entrapment did occur in a patient two years of age, the majority of the deaths and injuries involved elderly patients. Patients at high risk for entrapment include those with pre-existing conditions such as confusion, restlessness, lack of muscle control, or a combination of these factors.

FDA recommends the following actions to prevent deaths and injuries from entrapment in hospital bed side rails:

Inspect all hospital bed frames, bed side rails, and mattresses as part of a regular maintenance program to identify areas of possible entrapment. Regardless of mattress width, length, and/or depth, alignment of the bed frame, bed side rail, and mattress should leave no gap wide enough to entrap a patient's head or body. Be aware that gaps can be created by movement or compression of the mattress which may be caused by patient weight, patient movement, or bed position.

Be alert to replacement mattresses and bed side rails with dimensions different than the original equipment supplied or specified by the bed frame manufacturer.(4) Not all bed side rails, mattresses, and bed frames are interchangeable. Variation in bed side rail design and thickness and/or density of the mattress may affect the potential for entrapment. When bed side rails and mattresses are purchased separately from the bed frame, check with the manufacturer(s) to make sure the bed side rails, mattress, and bed frame are compatible.

Check bed side rails for proper installation using the manufacturer's instructions to ensure a proper fit (e.g., avoid bowing, ensure proper distance from the headboard and footboard).

Additional safety measures should be considered for patients identified as high risk for entrapment. Such patients include those with altered mental status (organic or medication related) or general restlessness. Increased risk also occurs when the patient's size and/or weight are inappropriate for the bed's dimensions. Bed side rail protective barriers may be used to close off open spaces in which these patients might accidently become entrapped. Follow the healthcare facility's procedures and/or manufacturers' recommendations/specifications for installing and maintaining bed side rail protective barriers for the particular bed frame and bedside rails used.

Bed side rails should not be used as a substitute for patient protective restraints. Patients who need a protective restraint, such as a vest or wrist/leg device, must be monitored frequently while wearing it.(5) If a protective restraint is used, follow your facility's protocol and the restraint manufacturer's instructions for proper use, in addition to the federal, state, and local regulations regarding the use of protective restraints.

FDA is interested in receiving reports concerning problems with hospital bed frames, bed side rails, mattresses, and any other medical device. The Safe Medical Devices Act of 1990 (SMDA) requires hospitals and other user facilities to report deaths, serious illnesses, and injuries associated with the use of medical devices. Healthcare workers should follow the procedures established by their healthcare facility for such mandatory reporting. Practitioners who become aware of any adverse event (i.e., death, serious illness, or injury) that may be related to a medical device product problem or malfunction should report it to their facility's contact person who is responsible for reporting these events to the FDA.

If an adverse event or device problem or malfunction is not reportable under SMDA, or if you do not work in a user facility that is required to report under SMDA, we encourage you to report directly to MedWatch, the FDA's voluntary reporting program.

Write to: Medical Product Reporting Program
MedWatch, HF-2
Food and Drug Administration
5600 Fishers Lane
Rockville, MD 20857
 

Phone: Medical Product Reporting Program at
1-800-FDA-1088
(also call for MedWatch information)

Modem: 1-800-FDA-7737
(9600 baud rate)

 

Getting more information:

If you have questions about this Notification, please contact FDA's  Division of of Small Manufacturers, International and Consumer Assistance (DSMICA) by e-mail at dsmica@fda.hhs.gov or by phone at 1-800-638-2041 or 301-796-7100
 

FDA Medical Device Public Health Notifications are available on the Internet. You can also be notified through email each time a new Public Health Notification is added to our web page. To subscribe, visit: http://service.govdelivery.com/service/subscribe.html?code=USFDA_39.

 

Sincerely yours,

D. Bruce Burlington, M.D.
Director
Center for Devices and Radiological Health
Food and Drug Administration
 

REFERENCES:

  1. U.S. Consumer Product Safety Commission, National Injury Information Clearinghouse, January 1994 - July 1995.
  2. 2. Great Britain Medical Devices Directorate. "Use of Hospital Bed Safety Sides and Side Rails," London: Department of Health, January 1994.
  3. Health and Welfare Canada, Health Protection Branch. Medical Devices Alert No. 107, "Hazards with Hospital Bed Split Side Rails."
  4. Roy, D. "Beds and Side Rails: How Safe are They?" Dimensions in Health Service, 67(4):10,14, May 1990.
  5. Department of Health and Human Services, Food and Drug Administration Safety Alert "Potential Hazards With Restraint Devices," July 15, 1992.