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Hospital Equipment

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Esophageal Dilator (Bougie) | Feeding Tube | Gastrointestinal Tube | Intraocular Pressure Device | X-ray Machine | General References

Esophageal Dilators (Bougies)

Description: An esophageal dilator, also referred to as a bougie tube, is used to dilate the esophagus of a patient in response to medical conditions or treatments that cause esophageal narrowing or tissue shrinkage.
Esophageal Dilator
Source: California Dept. of Health Services, (esophageal dilators with mercury weights)
The dilator is a long, flexible tube that is slipped down the patient's throat into the esophagus, where it remains in place for several minutes before it is extracted. Older esophageal dilators consist of thick latex-coated tubing with approximately 2-3 pounds (more than 1,000 grams) of elemental mercury at the bottom of the tube.

Purpose of the Mercury: The mercury in esophageal dilators is used as a weight at the bottom of the tube. The density and liquid properties of mercury make it ideal to use as a flexible weight, necessary to insert the tube into the patient's constricted esophagus.

Potential Hazards: Over time, the latex covering of the esophageal dilator tubing can become brittle and cracked, which may lead to a mercury release. Older mercury-containing esophageal dilators have been known to rupture during handling or use causing potential environmental, patient, and employee hazards. This is the reason that mercury-containing esophageal dilators have an expiration date.

The large amount of mercury contained in esophageal dilators would present a significant risk of exposure as well as extensive cleanup costs if spilled. Spills greater than one pound of elemental mercury (about two tablespoons) must be reported to the appropriate state environmental agency. If a leak or break occurs, persons should immediately contact their state environmental agency for instructions on proper clean-up and disposal. Persons that have been exposed to a mercury spill should also contact the public health department or poison control center.

Recycling/Disposal: Out-of-service mercury-containing medical devices must be disposed of as hazardous waste through a licensed hazardous waste facility. The mercury collected from the esophageal tubes should be sent to a reclamation facility and recycled.

Statutes and Other Information: The amount of mercury contained in esophageal dilators and bougie tubes makes these products subject to sales restrictions in certain states, including Connecticut, Louisiana, and Rhode Island. Esophageal dilators are also subject to sales restrictions in other states, including California, Illinois, Maine, Massachusetts, Minnesota, New Hampshire, New York, and Vermont. These states do allow manufacturers to apply for an exemption, which, if approved, would allow them to sell these products in the state after the effective phase-out date.

Mercury-filled esophageal dilators and bougie tubes are becoming rare, and research has not identified any companies that still manufacture these devices. Instead, water- and tungsten-filled dilators are now commonly used.

Related Links:
http://www.govlink.org/hazwaste/mercury/MedicalEquipment.html#Esophageal
http://www.p2000.umich.edu/mercury_reduction/mr1.htm

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Feeding Tubes

Description: A feeding tube is a medical device used to provide nutrition to patients that cannot obtain nutrition by swallowing. They are used to administer food or drugs. The most common feeding tube is the nasogastric tube, which is passed through a patient's nose, past the throat, and into the stomach. The tubes are usually made of polyurethane and silicone. Older tubes can contain a small amount of mercury as a weight at the bottom of the tube, which helps guide the tube into place.

Purpose of the Mercury: The weight of the mercury guides the tube into place using gravity.

Potential Hazards: The polyurethane coating of a feeding tube is not easily broken during normal handling. However, if a leak or break occurs, persons should immediately contact their state environmental agency for instructions on proper clean-up and disposal. Persons that have been exposed to a mercury spill should contact the public health department or poison control center.

Recycling/Disposal: Out-of-service mercury-containing medical devices must be disposed of as hazardous waste through a licensed hazardous waste facility. The mercury collected from the feeding tubes should be sent to a reclamation facility and recycled.

Statutes and Other Information: The amount of mercury contained in weighted feeding tubes (greater than one gram) would make these products subject to sales restrictions in certain states, including Connecticut, Louisiana, and Rhode Island.

Weighted feeding tubes are no longer common and the few that are currently manufactured and sold in U.S. do not contain mercury - they use tungsten as a weight.

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Gastrointestinal Tubes

Description: A gastrointestinal tube is used to eliminate intestinal obstructions. Types of gastrointestinal tubes include Miller Abbott, Blakemore, and Cantor tubes. The tube is passed down a patient's esophagus, through the stomach, and into the small intestine to help remove or reduce intestinal obstructions. Historically, these tubes had a balloon containing mercury as the flexible weight, which would help guide the tube into place. When filled to capacity, these devices contained approximately 2 pounds (1,000 grams) of mercury.

Purpose of the Mercury: The weight of the mercury guides the tube into place using gravity.
Gastrointestinal Tube
Click image for a larger view
Source: California Dept. of Health Services, (Blakemore gastrointestinal tube)

Potential Hazards: The large amount of mercury contained in gastrointestinal tubes would present a significant risk of exposure as well as extensive cleanup costs if spilled. Spills greater than one pound of elemental mercury (about two tablespoons) must be reported to the appropriate state environmental agency. If a leak or break occurs, persons should immediately contact their state environmental agency for instructions on proper clean-up and disposal. Persons that have been exposed to a mercury spill should contact their public health department or poison control center.

Recycling/Disposal: Out-of-service mercury-containing medical devices must be disposed of as hazardous waste through a licensed hazardous waste facility. The mercury collected from the gastrointestinal tubes should be sent to a reclamation facility and recycled.

Statutes and Other Information: The amount of mercury contained in gastrointestinal tubes (greater than one gram) would make these products subject to sales restrictions in certain states, including Connecticut, Louisiana, and Rhode Island.

Gastrointestinal tubes filled with mercury are no longer widely used in the medical industry and no manufacturers of mercury-containing gastrointestinal tubes have been identified. New gastrointestinal tubes are manufactured and sold un-weighted (i.e., the hospital must supply their own weight, such as sterile water) or with tungsten gel as the weight.

Related Link:
http://www.govlink.org/hazwaste/mercury/MedicalEquipment.html#Gastrointestinal

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Intraocular Pressure Devices

Description: Small bags of mercury were historically used as weights to apply pressure to the eye prior to cataract surgery. These mercury-filled balloons, which were the size of a small egg, contained approximately 175 grams of elemental mercury that was double or triple bagged and placed on the patient's eye prior to surgery.

Purpose of the Mercury: When placed on the eye, the weight of the mercury on the eyeball kept fluid from accumulating at the normal rate, softening the eyeball prior to surgery. This practice reduced the pressure within the eyeball, simplifying surgery. However, this method is no longer used.

Note: as the need for these devices decreased, they were often shoved to the back of cabinets or drawers and forgotten about. Therefore, some effort must be exerted to search for these unused items and to properly dispose of them.

Potential Hazards: These mercury-filled balloons can be easily broken or ruptured - especially as they get older and the integrity of the rubber balloon degrades. If a leak or break occurs, persons should immediately contact their state environmental agency for instructions on proper clean-up and disposal. Persons that have been exposed to a mercury spill should contact the public health department or poison control center.

Recycling/Disposal: Out-of-service mercury-containing medical devices must be disposed of as hazardous waste through a licensed hazardous waste facility. The mercury-filled intraocular pressure devices should be sent to a reclamation facility and recycled.

Statutes and Other Information: Intraocular mercury pressure reducers are no longer commercially available, and the practice of weighting the eye is largely obsolete. New techniques and less invasive tools for surgery mean that pressure reduction is not always necessary, and the practice of weighting the eye prior to cataract surgery is less common.

Related Link:
http://www.govlink.org/hazwaste/mercury/MedicalEquipment.html#Eyesurgery

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X-Ray Machines

Description: X-ray machines can contain small mercury leveling switches as part of the positive beam limitation (PBL) system, also referred to as the automatic collimation system, which is mounted on the x-ray tube housing. Collimation refers to the process of adjusting an optical instrument (i.e., x-ray machine) to ensure the best possible image quality. The PBL system is an automatic collimation system used in stationary radiographic equipment. The mercury switches in this system usually account for approximately 3-4 grams of mercury per machine, although some may contain significantly more. For example, the Department of Health Services in California encountered an x-ray machine with almost eight grams of mercury when they completed a hospital mercury assessment.

X-Ray
Click image for a larger view
Source: National Health and Nutrition X-ray Procedures Manual, (diagram of PBL collimator)
Purpose of the Mercury: A positive beam limitation system (PBL) uses four miniature mercury switches to assure perpendicularity between the x-ray beam and the film and maintain precise control over the radiation beam.

Potential Hazards: As long as the system remains intact, there is a low probability that there would be a mercury release from this device.

However, x-ray machines may contain other sources of mercury in the x-ray film and chemical processing solutions (e.g., fixer). Therefore, care should be taken whenever handling this equipment to prevent a mercury release.

Recycling/Disposal: The PBL system, or collimator, should be removed from the x-ray machine for proper disposal. It is relatively easy to remove and there is no major disassembly needed. Out-of-service mercury-containing medical devices must be disposed of as hazardous waste through a licensed hazardous waste facility. A professional service technician will be able to safely remove the mercury switches from the equipment and send them to a mercury reclamation facility for recycling.

It is also important to note that since the PBL collimator system contains lead, the entire device should be disposed of as hazardous waste.

Statutes and Other Information: In many states, including California, Connecticut, Illinois, Louisiana, Maine, Massachusetts, Minnesota, New Hampshire, New York, Rhode Island, and Vermont, mercury switches are among the list of mercury-added products that are prohibited for sale - whether they are sold alone or as components of another product. These states however, do allow manufacturers to apply for an exemption, which, if approved, would allow them to sell these products in the state after the effective phase-out date.

Previously, Federal Regulation 21 CFR Part 1020 required automatic beam leveler switches to be present in virtually all x-ray machines. However, the PBL system is no longer required by federal regulations and existing systems may be overridden by the operator. These systems may simply be removed and do not need to be replaced. Persons should first review the state regulations to determine if PBL collimator systems are still required by their State Department of Health.

Related Links:
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?CFRPart=1020&showFR=1
http://www.dtsc.ca.gov/PollutionPrevention/upload/guide-to-mercury-assessment-in-healthcare-facilities.pdf

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General References

The links below are general references that provide information pertaining to all mercury-containing products found in hospitals and health care facilities:

General Information about Mercury-Containing Medical Devices:
http://www.dtsc.ca.gov/PollutionPrevention/upload/guide-to-mercury-assessment-in-healthcare-facilities.pdf
http://www.sustainableproduction.org/downloads/An%20Investigation%20Hg.pdf

Alternatives to Mercury-Containing Medical Devices:
http://www.sustainablehospitals.org/HTMLSrc/IP_Merc_Tools_List.html

Hospital Mercury Education and Reduction Programs:
http://www.epa.gov/grtlakes/bnsdocs/merchealth
http://www.sustainablehospitals.org/HTMLSrc/IP_Mercury.html
http://cms.h2e-online.org/ee/hazmat/hazmatconcern/mercury
http://www.noharm.org/us/mercury/issue

Mercury Product Phase-outs, Sales Prohibitions, and Exemptions:
http://www.newmoa.org/prevention/mercury/imerc/productban.cfm
http://www.newmoa.org/prevention/mercury/imerc/phaseoutinfo.cfm

Spill Clean-up Guidance:
http://www.mass.gov/dep/toxics/stypes/spill.pdf

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Last Modified 12/02/2008


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