F 0644
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Coordinate assessments with the pre-admission screening and resident review program; and referring for
services as needed.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
medical record review and staff interview, the facility failed to ensure a Pre-admission Screening and
Resident Review (PASRR) document accurately reflected medications and a psychiatric hospitalization.
This affected one (Resident #37) of four residents reviewed for PASRR documents. The census was 46.
Findings Include:
Medical record review revealed Resident #37 was admitted to the facility on [DATE] with diagnoses
including metabolic encephalopathy, Alzheimer's disease, major depressive disorder, delusional disorder,
dementia with psychotic disturbance, and panic disorder.
Review of the annual Minimum Data Set (MDS) 3.0 assessment, dated 07/19/24, revealed the resident was
severely cognitively impaired and received an anti-anxiety medication.
Review of Resident #37's PASRR document, dated 08/26/24, revealed under Section E, no anti-anxiety
medication. Review of the resident's physician orders, dated 03/29/24, revealed the order for Xanax 0.5
milligrams (mg) to be administered three times per day. Review of the medication administration record
(MAR), dated August 2024, revealed the resident received this medication as ordered. Further review of the
PASRR document under Section E, incorrectly indicated the resident had not been hospitalized for inpatient
psychiatry. Review of Resident #37's medical record revealed the resident was hospitalized on [DATE] due
to increased confusion, paranoia, believing he was breaking up a prostitution ring, making sexual
comments to staff, delusions, grandiosity, and having trouble sleeping.
During interview on 09/03/24 at 4:41 P.M., Social Services Designee (SSD) #194 confirmed Resident #37's
PASRR document was not accurate and did not indicate the use of an anti-anxiety medication nor the
inpatient psychiatric hospitalization on 03/11/24.
Any deficiency statement ending with an asterisk (*) denotes a deficiency which the institution may be excused from correcting providing it is determined that other
safeguards provide sufficient protection to the patients. (See instructions.) Except for nursing homes, the findings stated above are disclosable 90 days following the
date of survey whether or not a plan of correction is provided. For nursing homes, the above findings and plans of correction are disclosable 14 days following the date
these documents are made available to the facility. If deficiencies are cited, an approved plan of correction is requisite to continued program participation.
LABORATORY DIRECTOR'S OR PROVIDER/SUPPLIER
REPRESENTATIVE'S SIGNATURE
TITLE
(X6) DATE
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Facility ID:
If continuation sheet
Page 1 of 7
Event ID:
366128
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
366128
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/05/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Altercare Cambridge Inc.
66731 Old Twenty-One Road
Cambridge, OH 43725
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0695
Provide safe and appropriate respiratory care for a resident when needed.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, resident interview, record review, policy review and staff interview, the facility failed
to ensure oxygen tubing was changed weekly and documented as administered in the medical record. This
affected one (Resident #8) of two residents reviewed for supplemental oxygen use. The facility census was
46.
Residents Affected - Few
Findings include:
Observations of Resident #8 on 09/03/24 at 9:26 A.M. revealed the resident lying in bed. Supplemental
oxygen was supplied by an oxygen concentrator (machine that separates nitrogen from atmospheric air
delivering 95% pure oxygen) via a nasal cannula. No evidence of any date to the tubing and nasal cannula
was observed. Additional observations of Resident #8 on 09/03/24 at 3:58 P.M., 09/04/24 at 7:38 A.M. and
09/04/24 at 12:05 P.M. revealed supplemental oxygen in use by Resident #8 with no date on the tubing.
Observation on 09/05/24 at 9:50 A.M. revealed Resident #8 sitting in her recliner and supplemental oxygen
lying on her bed with the tubing undated.
Interview with Resident #8 on 09/05/24 at 9:50 A.M. revealed that she uses the supplemental oxygen when
in bed every day. She could not recall when the oxygen tubing was replaced.
Review of Resident #8's medical record revealed an admission date of 01/15/24 with diagnoses that
included chronic obstructive pulmonary disease, Parkinson's disease and cerebrovascular accident. Further
review of the medical record including Minimum Data Set (MDS) 3.0 significant change assessment with a
reference date of 08/09/24 indicated Resident #8 had an independent and intact cognition level and used
supplemental oxygen therapy.
Physician's orders for Resident #8 indicated on 08/03/24 an order for two liters of supplemental oxygen as
needed for a blood oxygen saturation level lower than 89%. No order was found related to replacing the
oxygen tubing routinely.
Progress notes revealed as needed supplemental oxygen was utilized by Resident #8 on
08/03/24, 08/05/24, 08/06/24, 08/07/24, 08/11/24, 08/12/24, 08/18/24, 08/20/24, 08/24/24, 08/25/24,
08/26/24, 08/27/24, 08/30/24 and 09/02/24. An additional progress note dated 08/11/24 indicated Resident
#8 uses the supplemental oxygen every night while sleeping. No evidence of changing the oxygen tubing
was found in the progress notes.
Review of the Medication Administration Record (MAR) revealed documentation of supplemental oxygen
administered as ordered on 08/03/24, 08/05/24, 08/17/24 and 09/01/24. No evidence of changing oxygen
tubing was found on the MAR.
On 09/03/24 at 3:20 P.M. interview with Licensed Practical Nurse (LPN) #133 indicated residents on
supplemental oxygen therapy have tubing changed weekly on Fridays by a contracted oxygen supply
company.
On 09/05/24 at 9:55 A.M. interview with the Director of Nursing verified Resident #8's oxygen tubing and
nasal cannula were not dated and unknown when last replaced. The DON also verified supplemental
oxygen use was not consistently documented as administered on the MAR.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366128
If continuation sheet
Page 2 of 7
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
366128
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/05/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Altercare Cambridge Inc.
66731 Old Twenty-One Road
Cambridge, OH 43725
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0695
Review of the facility policy titled Respiratory Treatment Oxygen dated 05/19/21 indicated to change oxygen
tubing, nasal cannula every seven days.
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366128
If continuation sheet
Page 3 of 7
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
366128
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/05/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Altercare Cambridge Inc.
66731 Old Twenty-One Road
Cambridge, OH 43725
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0698
Provide safe, appropriate dialysis care/services for a resident who requires such services.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
record review, review of a meal ticket, observation, resident interview, staff interview, and policy review, the
facility failed to ensure there was consistent communication between the facility and the dialysis center
regarding a resident's hemodialysis treatments. They also failed to ensure the medical record accurately
reflected the resident's current order for a fluid restriction and staff were knowledgeable about the resident's
need for a fluid restriction as ordered for end stage renal disease. This affected one (Resident #19) of one
resident reviewed for dialysis.
Residents Affected - Few
Findings include:
1 a.) Review of Resident #19's medical record revealed the resident was admitted to the facility on [DATE].
Her diagnoses included end stage renal disease, dependence on renal dialysis, pulmonary hypertension,
and congestive heart failure.
Review of Resident #19's physician's orders revealed the resident had an order for dialysis treatments
every Monday, Wednesday, and Friday. The order originated on 08/19/23.
Review of Resident #19's active care plans revealed she had a care plan in place for an alteration in renal
function, as the resident was receiving renal dialysis. The care plan was initiated on 06/28/23 and indicated
the facility was to encourage the dialysis center to forward dialysis treatment notes to the facility.
Review of Resident #19's medical record revealed it was absent for most of the dialysis visit notes for the
resident's dialysis treatments she received in the past 30 days. Out of the 14 times the resident was sent
out of the facility for a dialysis treatment, 13 of those visits did not have a dialysis visit note to indicate what
the resident's pre-weight and dry weight (weight after dialysis) were, what her vital signs were, what
medications she had been given, and how the resident tolerated the dialysis treatment during each visit.
On 09/03/24 at 2:22 P.M. an interview with Resident #19 revealed she did not believe the facility was
sending her to the dialysis center with any paperwork. She also denied the dialysis center had sent her
back to the facility with any dialysis visit notes. She did not feel the facility and the dialysis center were
communicating as well as they should.
On 09/04/24 at 3:02 P.M., an interview with LPN #133 revealed the facility's nurses completed dialysis
observation assessments on Resident #19 before and after she had her dialysis treatments. She denied
those dialysis observation forms that were completed were sent with the resident to dialysis. She further
denied the resident was sent back to the facility with any dialysis visit notes. Any communication made
between the dialysis center and the facility would be done by the dialysis center calling them. She indicated
they may get a call from the dialysis center on occasion, if there was a new order or a change in the
resident's condition. She denied the facility would know what the resident's weights and vital signs were pre
and post-dialysis. They would also not know what medications the resident received while at dialysis, or
how she tolerated the treatment.
On 09/05/24 at 10:10 A.M., findings were verified by the Director of Nursing (DON) and RN #220 that
Resident #19's electronic medical record (EMR) did not show evidence of consistent and adequate
communication occurring between the facility and the resident's dialysis center. They acknowledged the
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366128
If continuation sheet
Page 4 of 7
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
366128
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/05/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Altercare Cambridge Inc.
66731 Old Twenty-One Road
Cambridge, OH 43725
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0698
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
dialysis center was not sending a dialysis visit note for the resident that let them know what the resident's
pre-weight and dry weight was when the resident received hemodialysis. There was also no communication
of any medications that may have been administered to the resident or how she tolerated the dialysis
treatment while there. They acknowledged their policy and the resident's plan of care indicated the facility
was to receive a dialysis visit note from the dialysis center when the resident received her treatments three
days a week.
The facility's dialysis policy updated 2024 was reviewed and revealed it was the policy of the facility that all
residents utilizing renal dialysis receive comprehensive interdisciplinary monitoring to ensure resident
safety and support of dialysis services. The dialysis center would send reports from the resident's dialysis
treatments to the facility after each visit.
1 b.) Review of Resident #19's medical record revealed the resident was admitted to the facility on [DATE].
Her diagnoses included end stage renal disease (ESRD), dependence on renal dialysis, pulmonary
hypertension, and congestive heart failure.
Review of Resident #19's physician's orders revealed the resident had an order in place for a 1,500 milliliter
(ml)/ day fluid restriction with directions for dietary to provide 1,000 ml and nursing to provide 500 ml to
equal the 1,500 ml/ day. The 500 ml allotted to nursing was further broke down to 250 ml on the day shift
and 250 ml on the night shift. The order had been in place since 04/26/24.
Review of Resident #19's active care plans revealed the resident had a care plan in place for an alteration
in renal function, as the resident was receiving renal dialysis for ESRD. The care plan was initiated on
06/28/23 and indicated the resident was on a 1,200 ml/ day fluid restriction with nursing and dietary dividing
fluids with meals and daily care including medication passes. The care plan intervention was not consistent
with what was specified in the physician's orders. That intervention for the 1,200 ml/ day fluid restriction had
been in place since 06/28/23.
Further review of Resident #19's care plans revealed she had another care plan in place for being at risk for
altered nutrition related to ESRD and being on hemodialysis. That care plan indicated the resident was on a
1,500 ml/ day fluid restriction, which was not consistent with what was indicated on the alteration in renal
function care plan. The care plan for the resident's risk for altered nutrition was last revised on 08/15/24.
Review of Resident #19's meal ticket for 09/05/24 revealed the resident was identified as being on a 1,200
ml fluid restriction. It did not break it down on the meal ticket to specify how much fluid the resident should
be given for each meal.
On 09/03/24 at 2:22 P.M. an observation of Resident #19 noted her to be in her room. She was noted to
have a can of pop in her room and a full Styrofoam cup of water. The resident was not sure if she was on a
fluid restriction or not for her dialysis.
On 09/05/24 at 8:06 A.M., an interview with State Tested Nursing Assistant (STNA) #144 revealed she was
not aware of Resident #19 being on a fluid restriction. She indicated they gave the resident the same
amount of water in her Styrofoam cup as the other residents received. She indicated the resident usually
did not drink all of what was given to her in her Styrofoam cup and thought she only drank about 240 ml
from it. She usually did drink what they sent on her meal trays. She then indicated, since the resident was
on dialysis, she likely was on a fluid restriction, as most of them were.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366128
If continuation sheet
Page 5 of 7
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
366128
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/05/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Altercare Cambridge Inc.
66731 Old Twenty-One Road
Cambridge, OH 43725
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0698
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
She did not know what amount of fluids the resident could have, if she was on a fluid restriction. She felt the
resident probably drank what she was able to, but did not know for sure, as they did not know what she
drank when out of the facility with her family.
On 09/05/24 at 10:10 A.M., findings were verified by the DON and RN #220 that Resident #19's care plans,
physician's orders, and meal ticket were unclear on the amount of the fluid restriction the resident was to be
on. They acknowledged the discrepancy in the amount of fluids that the resident could have as documented
on her two care plans, physician's orders, and meal ticket. They confirmed the resident's current order was
for a 1,500 ml/ day fluid restriction and the care plans and meal ticket should all reflect such. They further
acknowledged the STNA interviewed, who was caring for Resident #19, was unaware she was on a fluid
restriction and was providing the resident water in a Styrofoam cup just like they did with all the other
residents.
Event ID:
Facility ID:
366128
If continuation sheet
Page 6 of 7
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
366128
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/05/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Altercare Cambridge Inc.
66731 Old Twenty-One Road
Cambridge, OH 43725
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0880
Provide and implement an infection prevention and control program.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, medical record review and staff interview, the facility failed to follow appropriate
transmission based precautions for a resident on contact precautions. The affected one (Resident #253) of
two residents identified on transmission based precautions. The facility census was 46.
Residents Affected - Few
Findings include:
Review of Resident #253's medical record revealed an admission date of 08/30/24 with diagnoses that
included enterocolitis due to clostridium difficile, sepsis, pneumonia and chronic obstructive pulmonary
disease. Physician's orders upon admission indicated Resident #253 required contact transmission based
precautions and resident to remain in his room related to signs of symptoms of a highly transmissible
disease or epidemiologically significant pathogen.
Observation on 09/04/24 at 2:20 P.M. revealed Activity Coordinator (AC) #192 in Resident #253's room. A
sign was posted on Resident #253's door frame indicating he was on contact precautions and a cart
containing personal protective supplies was noted below the sign and outside the resident's room door. AC
#192 was sitting on the edge of Resident #253's bed and was wearing a protective gown and gloves. The
gown was tied twice in the back but was open with approximately a three to four inch opening with AC
#192's pants contacting the linens of Resident #253's bed. Resident #253 was observed sitting in a recliner
next to the bed. Resident #253 was observed in the bed earlier in the day.
On 09/04/24 at 2:22 P.M. interview with AC #192 indicated she was completing an activity assessment for
Resident #253. She verified the resident had contact precautions in place for C-Diff and should not have
been sitting on the residents bed with her personal clothing exposed and contacting the bed linens.
On 09/04/24 at 2:40 P.M. AC #192 indicated she changed into new nursing scrubs after informing the
Director of Nursing and Administrator of the incident.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366128
If continuation sheet
Page 7 of 7