F 0577
Allow residents to easily view the nursing home's survey results and communicate with advocate agencies.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, interview, and record review the facility failed to have the State inspection survey
results readily available and accessible to residents, family members and legal representatives. This
deficient practice affects all ten (R3, R9, R17, R27, R52, R58, R60, R66, R85 and R94) residents reviewed
for Resident rights to Survey results in a sample of 20 residents.
Residents Affected - Many
Findings include:
On 4/18/24 at 10:23am during Resident council meeting held with ten residents in attendance, all ten
residents stated that they are not aware of where the State Inspection results binder is located. All stated
that they have not seen the signage for the location of the survey results.
On 4/18/24 at 11:05am, V28(Office Manager) stated that she does not know where the State Inspection
Survey results binder is and has not seen it at the front desk. She was unable to locate the Survey results
binder at the front desk during the interview.
On 4/18/24 at 11:10am, V1(Administrator) stated that the binder is usually located at the front desk. V1 and
V21 (Assistant Administrator) both could not find the binder after looking for approximately five minutes. V1
stated I will look for it.
Facility's policy on Resident Rights with no review date states: The facility will inform the resident both orally
and in writing, in a language that the resident understands, of his or her rights and all rules and regulations
governing resident conducts and responsibility during the stay in the facility . 6. Information and
Communication. k. The resident has the right to: i. Examine the results of the most recent survey of the
facility conducted by Federal or State surveyors and plan of correction in effect with respect to the facility .
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 5
Event ID:
145898
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
145898
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bria of Chicago Heights
120 West 26th Street
South Chicago Height, IL 60411
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 0684
Provide appropriate treatment and care according to orders, resident’s preferences and goals.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record review the facility failed to follow their hypoglycemia protocol by not administering
glucagon to a resident (R248) with a low blood sugar that was unresponsive for one (R248) out of three
residents reviewed for change in condition in a total sample of 20.
Residents Affected - Few
Findings Include:
R248 is a [AGE] year old with the following diagnosis: type 2 diabetes, metabolic encephalopathy, and
hemiplegia following a cerebral infarction.
A Nursing note dated 1/23/24 documents R248 was observed unresponsive to verbal stimuli. Supplemental
oxygen was placed on R248 at 3 L via nasal cannula. 911 was called and R248 was transported to the
hospital.
A Change in Condition dated 1/23/24 documents R248 was sent to the hospital for altered mental status.
The most recent blood glucose test at 9:15AM was 45. There's no documentation that any interventions
were performed to address the low blood sugar before the ambulance arrived.
The Fire Department record dated 1/23/24 documents the paramedics arrived on scene at 9:13AM for a
call of an unresponsive resident that was found ten minutes prior. The first set of vital signs were pulse 144
(normal is 60 to 100), blood pressure 126/78, respiratory rate 24 (normal 12-16), and oxygen level was
95% on room air. Upon arrival, granulated sugar was found in R248's mouth and staff confirmed pouring
sugar in R248's mouth when the blood sugar was 60. Glucose was tested at 9:16AM and was 20 (normal
blood sugar is 60-100). Intramuscular glucagon was given, and the blood sugar was still low but came up to
48. R248 had a slight improvement to responsiveness at this time.
The Hospital Records dated 1/23/24 document R248 arrived to the emergency department at 9:37AM and
came in due to being unresponsive after blood sugar was found to be in the 20s by EMS. While in route,
EMS gave R248 glucagon, and the blood sugar improved to the 40s. In the ER, R248 was given 1 ampule
of D50 and R248 had better improvement to responsiveness. R248 was admitted to a general medicine
floor with a diagnosis of hypoglycemia.
On 4/17/24 at 2:29PM, V4(RN) stated V4 was passing morning medication when V16 (CNA) alerted V4 that
R248 was unresponsive. V4 reported finding R248 unresponsive and when the blood sugar was checked, it
was in the 40s. V4 stated V4 called 911 and a code blue and waited for the ambulance. V4 denied giving
R248 glucagon because it wasn't in the med cart. V4 reported that is normally where glucagon is kept, and
it was not there so V4 stayed with R248 until ambulance arrived. V4 stated when the ambulance arrived,
they gave R248 glucagon and took R248 to the hospital. V4 said, Usually the rule is if they are alert, and
their blood sugar is below 80 then you give them some juice to drink to bring it back up. If they are not alert,
then you give glucagon. We didn't have any, so I didn't give any.
On 4/17/24 at 4:53PM, V16 stated V16 was passing breakfast trays in the morning and noticed R248 was
not responding as much as normal. V16 told V4 about R248 having a change in condition and V16
continued passing trays. V16 reported R248 is able to state R248's needs but this morning R248 was not
able to speak.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145898
If continuation sheet
Page 2 of 5
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
145898
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bria of Chicago Heights
120 West 26th Street
South Chicago Height, IL 60411
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 0684
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
On 4/17/24 at 5:04PM, V17 (Nurse) stated R248 did not show any signs or symptoms of hypoglycemia the
night before and was sleeping at 5AM during the last rounds. V17 reported nurse's have to give glucagon if
the resident's blood sugar is low (less than 60) and they are not responding. V17 stated, if the resident is
alert and the blood sugar is low then orange juice is given and to retest again in about 30 minutes. V17
reported glucagon is stored in the pyxis in the medication room and that is where staff need to go to get the
medication during an emergency.
On 4/18/24 at 9:49AM, V2 (DON) stated V16 was passing breakfast trays and found R248 unresponsive. V2
reported V16 told V4 and V4 found the blood sugar to be low. V2 stated if blood sugar is low, and a resident
is unresponsive then glucagon must be given to help raise the blood sugar. V2 reported in this situation
glucagon should have been given due to R248 being unresponsive and the blood sugar being in the 40s.
V2 stated glucagon is located in the emergency medication box in the medication room that all nurses have
access to.
The Physician Order Sheet documents an order for blood sugar checks to be done three times a day. There
was an order for Humalog insulin placed on 1/7/24. That is a sliding scale to be given with meals.
Instructions in the medication order document to notify the physician and initiate the hypoglycemia protocol
if blood sugar is less than 70.
The Medication Administration Record dated 01/2024 documents the sliding scale Humalog insulin ordered
blood sugar checks with each dose to be given. The blood sugar on 1/23/24 at 7:30 AM was 45.
The blood sugar was noted to be low at 45 when taken at 9:15AM on 1/23/24 per the vital sign's
documentation.
The SBAR Communication Form dated 1/23/24 documents R248 had an altered mental status that began
this morning. R248 is a diabetic and had a blood sugar of 45. R248 has an altered level of consciousness.
The Hospital Transfer Form dated 1/23/24 documents the key reason for transfer was respiratory arrest.
R248 has a heart rate of 146, respiratory rate of 24, blood pressure of 115/81, and oxygen level of 97%.
R248 was alert but not oriented and cannot follow simple instructions. R248 does not have any skin
concerns. 3 L of oxygen via nasal cannula was given. R248 was unresponsive and lethargic. Neither of
these forms have any documentation addressing what the facility did for the low blood sugar while waiting
for the ambulance.
The Care Plan dated 12/6/23 documents R248 is at risk for hypo/hyperglycemia related to type 2 diabetes.
An intervention documented is to monitor/document/report to the physician any signs or symptoms of
hypoglycemia that includes sweating, tremors, increased heart rate, nervousness, confusion, slurred,
speech, lack of coordination, and staggering gait.
The policy titled, Hypoglycemia Protocol, dated 09/2022 documents, General: To provide guidelines for
residents who were presenting with hypoglycemia signs and symptoms. 1. Hypoglycemia is defined as
blood glucose of less than 70 .3. If semiconscious, unconscious, uncooperative, unable to swallow, or is
NPO: administer 50 mL of D50W (1 amp) slow push and start IV D5W at 100 mL/hour. If no IV access:
Glucagon 1 mg subcutaneously or IM, then establish an IV access and start IV D5W at 100 mL/hour.
Repeat glucose, check and treatment every 15 minutes until greater than 70 mg/dL.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145898
If continuation sheet
Page 3 of 5
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
145898
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bria of Chicago Heights
120 West 26th Street
South Chicago Height, IL 60411
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 0761
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Many
Ensure drugs and biologicals used in the facility are labeled in accordance with currently accepted
professional principles; and all drugs and biologicals must be stored in locked compartments, separately
locked, compartments for controlled drugs.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. On [DATE]
at 2:55PM, this surveyor asked V2 (DON) to open the pyxis to show the surveyor the glucagon. V2 stated
the emergency medication box is located in the cabinet in the medication room. At 3:07PM, V2 opened the
cabinet that housed the emergency medication box and showed the surveyor two glucagon syringes. The
expiration date of both glucagon syringes was documented as 03/2024. V2 stated that medication should
have been discarded at the end of 03/2024 and should've been replaced with glucagon that is not expired.
V2 reported no residents should be given expired medication even in an emergency situation.
There are currently 13 residents in the facility that get their blood sugar checked and are prescribed insulin.
This expired medication can affect all 13 residents.
On [DATE] at 9:49AM, V2 stated the emergency box is pharmacy's responsibility to remove expired
medication. V2 reported the facility is responsible for checking the med carts and the med room while the
pharmacy is responsible for the pyxis and medication cabinet. V2 said the emergency medication box
should be checked every month. V2 was unaware if pharmacy checked the emergency medication box last
month.
On [DATE] at 12:03PM, V15 (Pharmacy Consultant) stated the pharmacy contracted with the facility is
responsible for coming to pick up the expired medication. V15 reported V15 runs a report in the pyxis each
month to see what medications need to be removed and then a list is compiled and sent to the pharmacy.
V15 stated the pharmacy is then responsible for coming to pick up the expired medication and replace it
with new medication. V15 reported last running the report on [DATE] and did not see glucagon on the report
of expired or soon to be expired medication. V15 denied checking the emergency medication box to see if
any medication was expired. V15 was unable to answer why the expired medication was not picked up by
the pharmacy.
The expired glucagon was photocopied. Both syringes are labeled glucagon emergency kit for low blood
sugar. Both syringes expired on 03/2024.
The policy titled, Storage of Medications, dated 09/2022 documents, Purpose: To provide the staff with
guidance on proper storage of medications . 11. Outdated, contaminated, or deteriorated medications - and
those in containers that are cracked, soiled or without secure closures should be immediately removed from
stock and disposed of according to medication disposal procedure. If necessary, medications should be
reordered from the pharmacy.
Based on observation, interview, and record review, the facility failed to label multi-dose medication for one
of two medication rooms observed for medication storage and labeling. This failure has the potential to
affect all 93 residents currently residing in the facility. The facility also failed to discard expired glucagon
from their emergency medication box. This deficient practice has the potential to affect all 13 diabetic
residents in the facility.
Findings include:
1. On [DATE] at 9:49AM during Medication Storage and Labeling observation with V2 (Director of Nursing),
the first-floor medication storage room was observed with two vials of opened, undated
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145898
If continuation sheet
Page 4 of 5
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
145898
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bria of Chicago Heights
120 West 26th Street
South Chicago Height, IL 60411
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 0761
Tuberculin, Purified Protein (Mantoux) 5TU/0.1ml, 10 dose vial.
Level of Harm - Minimal harm
or potential for actual harm
During an interview on [DATE] at 10:05AM with V2, V2 stated that she confirmed with pharmacy that the
multi-dose vials should be labeled with an open or accessed, and discard date 28 days unless
manufacturer specifies a different (shorter or longer date) as stated in the facility policy.
Residents Affected - Many
Facility policy titled: 5.21: Vials and Ampules and Guideline Storage of Medications. All vials and ampoules
of injectable medications are used in accordance with the manufacture's recommendations. 6. Expiration of
multi-dose vials. a. If a multi-dose vial has been opened or accessed, the vial should be dated and
discarded within 28 days unless manufacturer specifies a different (shorter or longer) date. b. If a multi-dose
vial has not been opened or accessed, it should be discarded according to the manufacturer's expiration
date.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145898
If continuation sheet
Page 5 of 5