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Inspection visit

Health inspection

ANTELOPE VALLEY CARE CENTERCMS #5554561 citation on this visit
1 citation recorded

Inspector’s narrative

What the inspector wrote

This survey cited 1 deficiency. The full statement and the facility’s plan of correction follow, verbatim from the federal record.

F 0760 Ensure that residents are free from significant medication errors. Level of Harm - Minimal harm or potential for actual harm Based on interview and record review, the facility failed to ensure one of three sampled residents (Resident 3) received medication as prescribed by failing to:1. Ensure Resident 3 received Eliquis (a prescription that prevents blood clots from forming and stops existing clots from getting bigger).2. Ensure Resident 3 received Femara (a medication that helps treat certain types of breast cancer)3. Ensure Licensed Vocational Nurse (LVN) 1 signed off the Medication Administration Record (MAR-a daily documentation record used by a licensed nurse to document medications and treatments given to a resident) after administering Resident 3's medications.These deficient practices had the potential for Resident 3 to be negatively affected.Findings:During a review of Resident 3's admission Record (AR), the AR indicated the facility admitted the resident on 7/2/2025 with diagnoses including chronic obstructive pulmonary disease (COPD--a chronic lung disease causing difficulty in breathing), with exacerbation (a worsening of symptoms or a flare-up of a disease or condition), other specified type of carcinoma (cancer that forms in tissue) in situations of unspecified breast, and atrial fibrillation (A-Fib a common heart condition where the heart's upper chambers [atria] beat irregularly and often rapidly).During a review of Resident 3's Minimum Data Set (MDS - a resident assessment tool), dated 7/9/2025, the MDS indicated Resident 3 can understand and be understood.During a review of Resident 3's Physician Orders, dated 7/2/2025, the Physician Orders indicated Femara tablet 2.5 milligrams (mg- a unit of measurement) give one (1) tablet by mouth one (1) time a day for breast cancer.During a review of Resident 3's Physician Orders, dated 7/3/2025, the Physician Orders indicated Eliquis oral tablet 5 mg give one (1) tablet by mouth every 12 hours for a-fib.During a review of Resident 3's History and Physical (H&P - comprehensive assessment conducted by a healthcare provider that includes gathering a thorough medical history from the resident and performing a physical examination to assess their overall health and identify any potential medical concern), dated 7/4/2025, the H&P indicated Resident 3 had the capacity to make decisions.During a review of Resident 3's care plan (a plan of care that summarizes a resident's health conditions, specific care and services facility staff need to provide a resident to promote healing and prevent a worsening of a condition, and current treatments) for the use of anticoagulant therapy (a treatment that uses medications to prevent blood clots from forming or growing larger), initiated on 7/13/2025, the care plan indicated Eliquis for a-fib. The care plan interventions included resident teaching to include the following take and give medication at the same time each day and to monitor, document and report to the doctor any signs or symptoms of anticoagulant complications.During a review of Resident 3's care plan, initiated on 7/13/2025, the care plan indicated impaired immunity related to cancer, resident has diagnoses of breast cancer and is taking femara. The care plan interventions included monitoring, document and reporting any sign and symptoms of infections. During a review of Resident 3's MAR for August 2025, the MAR indicated on:8/1/2025 (scheduled at 7 a.m.) for Femara tablet 2.5 mg give 1 table by mouth one (1) time a day for breast cancer indicated 9(9-other or see nurses notes).- 8/4/2025 (for the scheduled time of 9 p.m.) Residents Affected - Few (continued on next page) 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 3 Event ID: 555456 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 555456 B. Wing A. Building (X3) DATE SURVEY COMPLETED 08/05/2025 NAME OF PROVIDER OR SUPPLIER STREET ADDRESS, CITY, STATE, ZIP CODE Antelope Valley Care Center 44567 North 15th St. West Lancaster, CA 93534 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 0760 Level of Harm - Minimal harm or potential for actual harm Residents Affected - Few Eliquis oral tablet 5 mg give one (1) tablet by mouth every 12 hours for a-fib indicated 9- 8/5/2025 (for the scheduled time of 9a.m.) Eliquis oral tablet 5 mg give one (1) tablet by mouth every 12 hours for a-fib indicated it was not signed off.During a review of Resident 3's Progress Notes, dated 8/1/2025 at 7:45 a.m., the Progress Notes indicated Femara tablet 2.5 mg medication was not available at this time, faxed refill request to pharmacy and awaiting arrival.During a review of Resident 3's Progress Notes, dated 8/4/2025 at 10:32 p.m., the Progress Notes indicated Eliquis oral tablet 5 mg was found after contacting Pharmacy.During an interview on 8/5/2025 at 10 a.m. with Resident 3, Resident 3 stated has been out of Eliquis. Resident 3 stated has also had issues with missing her Famara which is her (Resident 3) cancer medication. Resident 3 stated she (Resident 3) is concerned because she (Resident 3) has had two blood clots, is trying to get better and wants to go home.During a concurrent interview and record review on 8/5/2025 at 10:17 a.m. of Resident 3's MAR with LVN 1, LVN 1 stated Resident 3 does not have Eliquis, not sure when Resident 3 received the last dose of Eliquis. LVN 1 reviewed Resident 3's MAR and stated Resident 3 received Eliquis on 8/4/2025 at 11:26 a.m. Resident 3 did not get her (Resident 3) evening dose. LVN 1 reviewed the medication cart and stated there is no Eliquis in the medication cart for the morning dose for Resident 3 there are doses for the evening dose. LVN 1 stated nurses are the ones in charge of ordering medication, should be ordering medications when there are 4 doses left. LVN 1 stated if Resident 3 is not getting her (Resident 3) Eliquis as prescribed can be a potential for Resident 3 to develop deep vein thrombosis (DVT-a blood clot that forms in a deep vein, usually in the leg or thigh) and blood clots. LVN 1 stated Resident 3 has now missed two doses with the morning dose.During a concurrent interview and record review on 8/5/2025 at 11:19 a.m. of Resident 3's Medication Bubble Pack (a pharmacy organized card that packages doses of medication within small, clear, or light-resistant, amber-colored plastic bubbles [or blisters]), with the Assistant Director of Nursing (ADON), the ADON stated the facility has the morning Eliquis for Resident 3. The ADON stated the number five (5) bubble was punched out because it was administered to Resident 3 today. During an interview on 8/5/2025 at 12 p.m. with Resident 3, Resident 3 stated she did get her Eliquis this morning, staff were able to find the Eliquis.During a concurrent interview and record review on 8/5/2025 at 1:30 p.m. of Resident 3's MAR with the Director of Nursing (DON), the DON reviewed Resident 3's MAR and stated Eliquis for 8/4/2025 for the p.m. dose was not given. The DON stated for the 8/5/2025 dose it was given this morning it was punched out on the bubble pack. The DON reviewed Resident 3's MAR and stated the MAR is not signed off indicating the Eliquis was given this morning (8/5/2025). The DON stated when administering medication should pour, pass, chart, should be signed the MAR right after resident takes medication. The DON stated the nurse should be giving the medications as scheduled and documenting them right away because it can cause Resident 3 to have side effects for not receiving medications as prescribed and it is inaccurate documentation. The DON reviewed Resident 3's MAR for Femara dated 8/1/2025 and stated Resident 1 did not get the medication that day. The DON stated the rule of thumb, and our policy is there needs to be three (3) days of supplies, nurses must reorder prior to the medication running out. The DON stated potential for not getting medication as prescribed can exacerbate the residents' condition, resident needs to be stable and not have complications, because for Eliquis there is a potential for clotting, and can be a potential for a-fib and risk to have clots. During a review of the facility's policy and procedure (P&P) titled, Medication and Treatment Orders, last reviewed on 5/30/2025, the P&P indicated drugs and biologicals that are required to be refilled must be reordered from the issuing pharmacy not less than three (3) days prior to the last dosage being administered to ensure that refills are readily available. During a review of the facility's P&P titled, Administering (continued on next page) FORM CMS-2567 (02/99) Previous Versions Obsolete Event ID: Facility ID: 555456 If continuation sheet Page 2 of 3 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 555456 B. Wing A. Building (X3) DATE SURVEY COMPLETED 08/05/2025 NAME OF PROVIDER OR SUPPLIER STREET ADDRESS, CITY, STATE, ZIP CODE Antelope Valley Care Center 44567 North 15th St. West Lancaster, CA 93534 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 0760 Level of Harm - Minimal harm or potential for actual harm Medications, last reviewed on 5/30/2025, the P&P indicated medications are administered in a safe and timely manner, and as prescribed.4. Medications are administered in accordance with prescriber orders, including any required time frames.22. The individual administering the medication initials the resident's MAR on the appropriate line after giving each medication and before administering the next one. Residents Affected - Few FORM CMS-2567 (02/99) Previous Versions Obsolete Event ID: Facility ID: 555456 If continuation sheet Page 3 of 3

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Citations

1 citation recorded*CMS

What do CMS severity letters mean?

Serious (G-L). Actual harm to a resident, or immediate jeopardy. Codes G through I indicate actual harm; J through L indicate immediate jeopardy to resident health or safety.

General (A-F). No actual harm found, or harm that is minimal. The facility must still submit a Plan of Correction. Most CMS citations land here.

Each letter combines severity with scope: how many residents the deficiency affected.

  • 0760GeneralS&S Dpotential for harm

    F760 - Residents are free of any significant medication errors

    Ensure that residents are free from significant medication errors.

FAQ · About this visit

Common questions about this visit

What happened during the August 5, 2025 survey of ANTELOPE VALLEY CARE CENTER?

This was a inspection survey of ANTELOPE VALLEY CARE CENTER on August 5, 2025. The surveyor cited 1 deficiency, recorded on the federal Form 2567 statement of deficiencies.

Were any deficiencies cited at ANTELOPE VALLEY CARE CENTER on August 5, 2025?

Yes, 1 deficiency was cited, each with a CMS Scope and Severity grade. The first was: "Ensure that residents are free from significant medication errors."

What type of survey was this?

This was a inspection survey conducted by state surveyors under federal Centers for Medicare & Medicaid Services (CMS) oversight. Findings are published on CMS Care Compare.

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Data from CMS Care Compare public records. Dataset last refreshed . If you believe any information is inaccurate, report it here.