Failure to monitor pacemaker function and obtain ordered wound culture from correct site
Summary
The facility failed to follow physician orders and care plan interventions for a resident with an implanted cardiac pacemaker and multiple cardiac diagnoses, including CHF, cardiomyopathy, atrial fibrillation, and dementia. The resident’s care plan addressed impaired cardiovascular status and included interventions such as administering medications as ordered, observing for CHF symptoms, monitoring weights, and providing oxygen as ordered, but there was no evidence of an intervention to check pacemaker function. The record also showed no evidence that the resident received the ordered daily weights on multiple days, and there was no documentation that the resident refused weights or that the physician or NP was notified when weights were not obtained. The resident experienced repeated episodes of decline while in the facility. At one point, staff documented lethargy, swelling, low oxygen saturation, abdominal distention, and blood in the catheter bag, leading to transfer to the hospital for urinary concerns and later acute on chronic CHF. The hospital records noted heart failure, pacemaker presence, and that daily weight monitoring was crucial. Later, the resident again became lethargic, clammy, sweaty, unable to swallow, and bradycardic, with oxygen saturation unobtainable. EMS transported the resident to the hospital, where bradycardia and pacemaker malfunction were identified, the pacemaker could not be properly interrogated because the battery may have died, and the resident required surgery for a new pacemaker implantation. Facility interviews and record review showed the resident had not had remote pacemaker checks completed in the facility during the relevant period, and staff were unaware of the pacemaker or how to complete the checks. The DON stated all residents with pacemakers should have pacemaker checks in place, and later found the resident’s remote monitoring device in the room unplugged and not working. The device clinic representative stated the bedside monitor needed to remain plugged in and that missed follow-up could occur when residents were lost in follow-up. The resident’s decline was described by staff and the POA as related to the pacemaker not working, and the resident was later discharged back to the facility after pacemaker replacement. The facility also failed to obtain a wound culture from the correct wound for another resident with a right lateral calf wound and a sacral pressure injury. The wound record showed the right lateral calf wound had necrotic tissue, large purulent drainage, deterioration, and signs and symptoms of infection, and a culture and sensitivity was ordered for that wound. However, the TAR documented that a wound culture was collected from the sacrum instead, and there was no documented evidence that the ordered culture from the right lateral calf wound was completed. The RDCS confirmed the specimen should have been collected from the right lateral calf wound and that it had been incorrectly collected from the sacrum.
Penalty
Resources
Below are regulatory guidelines relevant to this citation:
Trusted data from CMS and state health departments
Every citation, penalty and Plan of Correction is sourced from public CMS records (latest release July 29, 2026) and official state health department websites — never guesswork.
In your survey window? See what surveyors are citing.
The Survey-Prep Report maps your facility's risk from 12 months of CMS and state citation data — what's being cited around you and what to check first. $129 one-time.