F 0552
Ensure that residents are fully informed and understand their health status, care and treatments.
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 its policy to inform and obtain consents prior to the
administration of psychotropic medication for two residents (R4 and R42) reviewed for psychotropic
medication.Findings include:R4 is a [AGE] year-old female who originally admitted to the facility on [DATE]
and continues to reside in the facility. R4 has multiple diagnoses including but not limited to the following:
type II DM, cellulitis of face, multiple fractures, sleep apnea, hyperlipidemia, sciatica, alcohol abuse,
schizoaffective disorder, and cocaine abuse.Per Physician Order Summary Report, R4 started Quetiapine
Fumarate (Antipsychotic) on 10/8/2025 and continues to receive medication. Per Psych: Consent for
Antipsychotics was signed and dated 10/15/2025. It is to be noted that R4 received an antipsychotic
medication for seven days before consenting to the medication.R42 is an [AGE] year-old female who
originally admitted to the facility on [DATE] and continues to reside in the facility. R42 has multiple
diagnoses including but not limited to the following: toxic encephalopathy, dysphagia, cognitive
communication deficit, need for assistance with personal care, multiple fractures, paranoid schizophrenia,
and dementia.Per Physician Order Summary Report, R42 started Clozapine on 9/9/2025 and continues to
receive medication. Per Psych: Consent for Antipsychotics was signed and dated 9/17/2025. It is to be
noted that R42 received an antipsychotic medication for eight days before consenting to the medication.On
11/19/2025 at 12:15PM, V2 (Interim Director of Nursing) said orders for psychotropic medications should
not be put in prior to obtaining a consent. I obtained the consent for R4 and R42 at their care plan meeting,
which is usually held 3-7 days after admission.Facility policy titled Psychotropic Medication Program with
review date of 1/2025 states in part but not limited to the following: The purpose of this policy is to ensure
the resident and/or resident representative are aware of the potential side effects and the facility obtains an
informed consent for the use of psychotropic medications. If a new order for psychotropic medication is
obtained, the resident or representative must be informed of the risks and benefits of the medication. The
facility must obtain informed consent. Once consent is obtained, the order will be entered into the medical
record.
Residents Affected - Few
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 4
Event ID:
146058
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
146058
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/20/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Aliya of Evanston
1300 Oak Avenue
Evanston, IL 60201
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 0759
Ensure medication error rates are not 5 percent or greater.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to administer medications as ordered and follow
the manufacturer's instructions for use. There were 25 opportunities with four errors resulting in a 16%
(percent) error rate. This failure applied to two (R18 and R29) of four residents observed during medication
administration.Findings include:R18 is an [AGE] year-old, female, admitted in the facility on 06/08/23 with
diagnoses of Bilateral Primary Osteoarthritis, Other Asthma, and Essential Hypertension. R18's POS
(Physician Order Sheet) documented:06/08/23: Advair Diskus Aerosol Powder Breath Activated 250-50
mcg/dose (microgram per dose) (Fluticasone-salmeterol) 1 (one) inhalation inhale orally every 12
hours.12/03/23: Spironolactone tablet 50 mg (milligram) give 1 tablet by mouth one time a day.08/12/25:
Voltaren Gel 1% (percent) (Diclofenac Sodium) apply to both knees and feet topically two times a day for
pain 2 (two) gram dose. On 11/17/25 at 10:50 AM, V11 (Registered Nurse, RN) was observed passing
medication on R18. It was observed that Advair Diskus was not administered. V11 stated he already
administered it and showed surveyor the inhaler. The inhaler that was shown to surveyor was the Incruse
Ellipta and not the Advair Diskus. In the MAR (medication administration record), V11 signed Advair as
given but did not actually give during medication pass. Spironolactone was also not given because the
medication was not available during medication pass. V11 stated Spironolactone was ordered last 09/25/25
and still waiting to be delivered to facility. At 11:43 AM, V11 is about to administer the Voltaren Gel on R18.
V11 donned gloves, took the Voltaren Gel and squeezed an ample amount to gloved hand and rubbed the
gel onto R18's right knee. Subsequently, he (V11) again squeezed a desirable amount to his gloved hand
and rubbed it on her (R18) left knee. Voltraren Gel was not applied to R18's feet as ordered. Also, the
amount applied on R18's knees did not indicate a 2 gram dose as ordered. R29 is a [AGE] year-old, male,
admitted in the facility on 04/17/23 with diagnoses of Cerebral Infarction due to Unspecified Occlusion or
Stenosis of Left Posterior Cerebral Artery and Type 2 Diabetes Mellitus with Hyperglycemia.R29's POS
dated 10/24/24 documented: Insulin Lispro Injection Solution 100unit/ml (unit per milliliter) inject 4 (four)
units subcutaneously (SQ) with meals for hyperglycemia AND inject as per sliding scale: if 150-199 =2;
200-249 = 3; 250-299 = 4; 300-349 = 5. Call MD (Medical Doctor) if >350 mg/dl (milligram per deciliter),
subcutaneously with meals for hyperglycemia. On 11/17/25 at 12:00 PM, V6 (RN) was observed
administering Insulin Lispro 2 units on R29. V6 stated that only 2 units should be given to R29 because his
blood sugar level was 167, and per sliding scale, only 2 units will be given. V6 was asked regarding the
Insulin Lispro 4 units SQ with meals as standing order. V6 replied, I only give the 2 units, I just followed the
sliding scale order, and not the other order of 4 units. The 4 units is just a reminder of the sliding scale
order. They actually go together. Review of progress notes showed no documentation related to Insulin
Lispro 4 units as to why it was not given. R29's care plan regarding diagnosis of Diabetes Mellitus insulin
dependent recorded:Intervention: Diabetes medication as ordered by doctor. Monitor/document for side
effects and effectiveness. On 11/18/25 at 3:04 PM, V2 (RN/Interim Director of Nursing) was asked
regarding administration of Voltaren Gel and insulin orders. V2 replied, For the Voltaren Gel, we have this
card dose where we put the gel for the ordered dose. If it's for knees and feet, that will be two grams per
application. For insulin orders, if there is a standing order for 4 units and sliding scale of let's say 2 units, the
two units should be given along with the 4 units. Nurse should follow the orders. V2 was also asked
regarding medications not given. V2 stated, When we give the medication, we sign. If the medication is not
available at the time of administration, we document in the MAR that it was not given. Then we call the
doctor and document any orders. Facility's policy titled Medication
Residents Affected - Few
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
146058
If continuation sheet
Page 2 of 4
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
146058
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/20/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Aliya of Evanston
1300 Oak Avenue
Evanston, IL 60201
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 0759
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Administration dated 3/2025 stated in part but not limited to the following:General: All medications are
administered safely and appropriately to aid residents to overcome illness, relieve and prevent symptoms
and help in diagnosis. Guideline:1. An order is required for administration of all medication. 7. Read each
order entirely. 13. Verify that the medication is being administered at the proper time, in the prescribed
dose, and by the correct route. 14. Prepare or pour each dose of medication using an appropriate
measuring device. 22. If medication is not given as ordered, document the reason on the MAR and notify
the Health Care provider if required. Manufacturer's guidelines in dosage and administration of Voltaren
Gel, dated July, 2009 documented in part but not limited to the following:2. Dosage and administration2.1
Dosing cardThe proper amount of Voltaren Gel should be measured using the dosing card supplied in the
drug product carton. The dosing card is made of polypropylene, like the tube cap containing Voltaren Gel,
but without the white colorant. The dosing card should be used for each application of drug product. The gel
should be applied within the oblong area of the dosing card up to the 2 gram or 4 gram line (2 g for each
elbow, wrist, or hand, and 4 g for each knee, ankle or foot). The dosing card containing Voltaren Gel can be
used to apply the gel. The hands should then be used to gently rub the gel into the skin. After using the
dosing card, hold with fingertips, rinse and dry. If treatment site is the hands, patients should wait at least
one (1) hour to wash their hands. Patient Instructions for UseApplying Voltaren Gel to knees, ankles, and
feet:2.To measure the right amount of Voltaren Gel, place the dosing card on a flat surface so that you can
read the print. If the print is backwards, flip dosing card over.3.Squeeze Voltaren Gel onto the dosing card
evenly up to the 4 gram line, making sure the gel covers the entire 4 gram area of the dosing card.4.Apply
the Voltaren Gel to your foot, ankle or knee. You can use the dosing card to apply the gel. The hands should
be used to gently rub the gel into the skin. Do not share the dosing card with another person.Make sure to
cover your entire foot, ankle or knee area with the gel. For example, cover the skin above, below, inside and
outside the knee cap. Remember that the foot includes the sole of your foot, the top of your foot and your
toes.
Event ID:
Facility ID:
146058
If continuation sheet
Page 3 of 4
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
146058
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/20/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Aliya of Evanston
1300 Oak Avenue
Evanston, IL 60201
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 0883
Develop and implement policies and procedures for flu and pneumonia vaccinations.
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 policy and procedure and offer pneumococcal
vaccinations to new residents within seven days. This failure applied to four (R16, R25, R32, and R45) of six
residents reviewed for vaccinations.Findings include:R16 is a [AGE] year-old male who originally admitted
to the facility on [DATE] and continues to reside in the facility. R16 has multiple diagnoses including but not
limited to the following: cerebral infarction, type II DM, obesity, epilepsy, sleep apnea, and acute kidney
failure.R25 is an [AGE] year-old female who originally admitted to the facility on [DATE] and continues to
reside in the facility. R25 has multiple diagnoses including but not limited to the following: rhabdomyolysis,
protein calorie malnutrition, HTN, cellulitis, CAD, and depression.R32 is a [AGE] year-old male who
originally admitted to the facility on [DATE] and continues to reside in the facility. R32 has multiple
diagnoses including but not limited to the following: muscle disorder, gait and mobility abnormalities, lack of
coordination, intracerebral hemorrhage, HTN, hemiplegia, dysphagia, and anxiety.R45 is a [AGE] year-old
female who originally admitted to the facility on [DATE] and continues to reside in the facility. R37 has
multiple diagnoses including but not limited to the following: venous insufficiency, gait and mobility
abnormalities, protein calorie malnutrition, acute respiratory failure, Type II DM, and COPD.R16, R25, R32,
and R45's Immunization Report shows no pneumococcal vaccine was offered or given since admission.On
11/19/2025 at 1:32PM, V12 (Infection Preventionist) said we do not offer the pneumococcal vaccine to new
admissions immediately upon entering our facility. Our process is to offer them at a scheduled clinic at a
later date. I have been in this role for about six months and since then we have not had a vaccine clinic. We
have our first vaccine clinic in about two weeks, and we will offer multiple vaccinations, including
pneumococcal.Facility policy titled Pneumococcal Vaccinations with review date of 1/6/2025 states in part
but not limited to the following: 1. All current residents or the resident's responsible party will be screened
and offered the pneumonia vaccine within the first week of admission and annually, if eligible.
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
146058
If continuation sheet
Page 4 of 4