US · guidance
CMS SOM App. H, Tag V120
CDC RR-05 as Adopted by Reference 42 CFR 494.30(a)(1)(i)
Use external venous and arterial pressure transducer filters/protectors for each patient
treatment to prevent blood contamination of the dialysis machines’ pressure monitors.
If the external transducer protector becomes wet, replace immediately and inspect the
protector. If fluid is visible on the side of the transducer protector that faces the machine,
have qualified personnel open the machine after the treatment is completed and check for
contamination. This includes inspection for possible blood contamination of the internal
pressure tubing set and pressure sensing port. If contamination has occurred, the machine
must be taken out of service and disinfected using either 1:100 dilution of bleach (300–600
mg/L free chlorine) or a commercially available, EPA-registered tuberculocidal germicide
before reuse.
Page 14 of 420
Change filters/protectors between each patient treatment, and do not reuse them. Internal
transducer filters do not need to be changed routinely between patients.
Interpretive Guidance § 494.30(a)(1)(i)
According to the CDC, external transducer protectors, which provide a protective barrier
between dialysis bloodlines and the dialysis machine, should not be reused. “Wet” (“wet with
blood or other fluid”) external transducer protectors must be changed immediately, and the side
of the external transducer protector that faces the machine should be inspected for visible fluid.
If the external transducers are wetted with blood, the staff should inspect the wetted transducer
to see if fluid has passed through. If fluid or blood is visible on the side of the transducer
protector that faces the machine, the machine must be opened by qualified personnel after the
dialysis treatment to allow the internal transducer to be inspected for contamination. This
includes inspecting the internal pressure tubing set and pressure sensing port for possible blood
contamination. Frequent blood pressure alarms or frequent requirements for adjusting the blood
level in the drip chamber can be indicators of contamination of the internal transducer filter.
Recognize that some bloodlines do not have external transducer protectors; this requirement
would not apply in those cases, except for changing the bloodlines between patients.
History
Rev.
Provenance
- Source
- cms.gov
- Retrieved
- 2026-07-22
- Edition
- som-2026-07-22
- Content hash
05273bba59b78a415bb2bb39ee22d0765fb91ac1e20ae7e197c4d0383d615c41
The link goes to the issuing authority’s own document — the one we read to produce this record. Where a source publishes whole titles rather than sections, your browser may need a moment to jump to the provision.
Unofficial copy of government-published law, reproduced from official sources with full provenance. Not an official publication; verify against official sources before relying on it in a filing. Records in the 'guidance' corpus, and only that corpus, are sub-regulatory (interpretive guidelines, survey procedures) and are not binding law. Validity bounds follow each jurisdiction's declared temporalBasis.