Technical Specs on Upcoming Changes to the MDS 10/1/2017 Presented - - PDF document

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Technical Specs on Upcoming Changes to the MDS 10/1/2017 Presented - - PDF document

2/22/2017 Technical Specs on Upcoming Changes to the MDS 10/1/2017 Presented by: Jane C. Belt, MS, RN, RAC-MT, QCP February 22, 2017 Faculty Disclosure I have no financial relationships to disclose I have no conflicts of interests to


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2/22/2017 1 Presented by: Jane C. Belt, MS, RN, RAC-MT, QCP February 22, 2017

Technical Specs on Upcoming Changes to the MDS 10/1/2017 Faculty Disclosure

  • I have no financial relationships to disclose
  • I have no conflicts of interests to disclose
  • I will not promote any commercial products or

services

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Requirements for Successful Completion

  • 1.0 contact hour will be awarded for this continuing nursing

education activity

  • Criteria for successful completion includes attendance for at

least 80% of the entire event. Partial credit may not be awarded

  • Approval of this continuing education activity does not imply

endorsement by AANAC or ANCC (American Nurses Credential Center) of any commercial products or services

American Association of Post-Acute Care Nursing (AAPACN)* is accredited as a provider of continuing nursing education by the American Nurses Credentialing Center’s Commission on Accreditation. *AAPACN d/b/a American Association of Nurse Assessment Coordination 3

Learning Objectives

  • Delineate the new MDS 3.0 items in

Sections N and P effective October 1, 2017

  • Review specifications as to the item sets

impacted by the new MDS 3.0 items

  • Discuss the importance and strategies about

the new items and the influence they may have on your MDS accuracy and survey

  • utcomes

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What’s New: Straight from CMS

MDS 3.0 Technical Information

December 22, 2016

  • A new version (V2.01.0) of the MDS 3.0 Data

Specifications was posted. This version scheduled to become effective October 1, 2017. This DRAFT version incorporates the changes identified for the DRAFT version (v1.15.0) of the MDS 3.0 item sets. New items have been added to Sections N and P, and there are a number of new Section S items as well. December 1, 2016

  • A new DRAFT version (v1.15.0) of the MDS 3.0 item

sets was posted and scheduled to become effective October 1, 2017

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Updating OBRA

  • Congress passed legislation to amend the

Federal Government Code of Regulations (Chapter 42 of the Health Code), section 483 dealing with Skilled Nursing/Nursing Facility

  • Those changes resulted in revisions to:

– Requirements of Participation (10/4/2016) and were massive – to be implemented in 3 phases: 1 = 11/28/16; 2 = 11/28/17; 3 = 11/28/19 AND – State Operations Manual (SOM), in particular Appendix P and Appendix PP (Guidance and Compliance) (Advance Copy 11/9/2016) AND 2/10/17

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The Whys for Change

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Improvements in Care, Safety, and Protections for LTC Residents

Policies are targeted

  • Reducing unnecessary hospital readmissions and infections
  • Improving the quality of care
  • Strengthening safety measures for residents

Strengthening rights of residents

  • Staff members are properly trained on caring for residents with

dementia and in preventing elder abuse

  • Staff members have the right skill sets and competencies to

provide person-centered care

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The Whys for Change

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Discharge planning

  • Consideration of the caregiver’s capacity
  • Giving residents information they need for follow-up after

discharge

  • Instructions are transmitted to any receiving facilities or

services Infection prevention and control program

  • Requiring an infection prevention and control officer
  • Antibiotic stewardship program
  • Antibiotic use protocols
  • System to monitor antibiotic use

Quick Word about Section S

  • Reserved for state-defined items
  • No Section S in federal MDS, but appears if state has

chosen to use the section - items defined by state States with Section S Items – October 1, 2017

Arkansas Maryland Ohio California Maine Pennsylvania Florida Mississippi South Dakota Illinois North Dakota Virginia Louisiana Nebraska Vermont Massachusetts New York West Virginia

Connecticut has terminated all Section S items

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Section S Specs

  • Detailed Report – 397 pages and lists:

– Item identification – Item text (label) – In which item subsets the item is activated – Item Values – Item Edits (errors) – Version Changes

  • If opening an MDS 10/1/17 or after, make

certain to have a section S if you’re in a listed state

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Section N – New Item in N0410

MDS 3.0 Nursing Home Comprehensive (NC) Version 1.15.0 Effective 10/01/2017 DRAFT

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  • N0410H. Opioids

No changes for N0410 instructions

  • Number of days
  • Pharmacological classification –

NOT how it is used

  • Look-back period 7 days or since

admission/entry or reentry if less than 7 days

  • Enter “0” if medication not

received by the resident in the last 7 days

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N0410 Medications Received

Where does the new N0410H appear?

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OBRA PPS

NH PPS (NP/PPS) NH start of therapy/DC (NSD) SB Discharge (SD) Comprehensive (NC) NH Discharge (ND, NOD) Quarterly (NQ) NH PPS (NP/PPS) NH Start of Therapy/DC (NSD) Swing bed PPS (SP) SB OMRA- Discharge (SOD) SB OMRA SOT/Discharge (SSD)

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Why Was N0410H Added to MDS?

Effective 11/28/2016 – Appendix PP SOM revisions

  • Quality of Care F309

– §483.25(k) Pain Management.

  • The facility must ensure that pain management

is provided to residents who require such services, consistent with professional standards

  • f practice, the comprehensive person-

centered care plan, and the residents’ goals and preferences.

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Overview of Pain Recognition and Management

  • Factors affecting pain recognition:

– Misunderstanding of indicators for, benefits and risks of, opioids and other analgesics; or – Mistaken belief that older individuals have a higher tolerance for pain; or that pain is an inevitable part

  • f aging, a sign of weakness, or a way just to get

attention – Communication issues due to illness or language and cultural barriers, need to be stoic about pain, and cognitive impairment

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Overview of Pain Recognition and Management

  • Known that opioids used for residents who are

actively dying, those with complex, chronic pain syndromes (> 3 months) that have not responded to non-opioid analgesics or other measures

  • Opioids should not be prescribed as first-line

treatment for chronic pain

  • Adverse consequences especially when resident is

receiving other medications with significant effects on the cardiovascular and central nervous systems.

– Careful dosing based on evaluating the drug effectiveness and occurrence of adverse consequences – Clinical record needs to reflect ongoing communication between the physician and the staff for optimal and judicious use of pain medications.

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Monitoring, Reassessment, and Care Plan Revision

  • Monitoring over time helps identify how well pain

is controlled relative to the resident’s goals

  • Ongoing evaluation of presence, increase or

reduction of pain is vital as is status of causes, response to pain interventions, and possible presence of adverse effects of treatment

  • Adverse consequences related to analgesics can
  • ften be anticipated and to some extent

prevented or reduced. For example, opioids routinely cause constipation, which may be minimized by appropriate bowel regimen

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Evidence About Opioid Therapy

  • Opioids can provide short-term benefits for

moderate to severe pain

  • Scientific evidence is lacking for the benefits to

treat chronic pain and are not well supported by evidence

  • Short-term benefits small to moderate for pain;

inconsistent for function

  • Insufficient evidence for long-term benefits in

low back pain, headache and fibromyalgia

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More New Items in Section N

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  • N0450A. Did the resident receive antipsychotic

medications since admission/entry or reentry or the prior OBRA assessment

  • N0410B. Has a gradual dose reduction (GDR) been

attempted?

  • N0410C. Date of last attempted GDR

continued

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N0450A., N0450B., N0450C.

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continued

N0450 (continued)

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  • N0450D. Physician documented GDR as clinically

contraindicated

  • N0410E. Date physician documented GDR as

clinically contraindicated

continued

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  • N0450D. and N0450E.

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Which MDSs Have N0450?

  • Comprehensive

OBRA

  • Quarterly

OBRA

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Why Do You Suppose N0450 Added?

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Continued CMS Quality Initiative of Reducing Antipsychotics Requirements of Participation revisions Appendix PP continued updating

National Partnership to Improve Dementia Care

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2011Q4 = 23.9%

  • 32.4%

2016Q3 = 16.1%

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Added to Appendix PP

Problems with adverse events related to medications warrants close monitoring

  • OIG report on Adverse Events (AEs):

– Occurs in 1 of 5 SNF residents – 37% related to medications – 66% of medication-related AEs were preventable – Often occurs due to substandard treatment or insufficient monitoring – Use of multiple medications complicates the determination of the primary cause of events

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Phase 1 – §483.45 Pharmacy Services

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  • Requires a drug regimen review (DRR) that

includes a resident’s MEDICAL RECORD monthly

  • Pharmacist must report: any irregularities

(includes, but not limited to any drug that meets the “unnecessary drug” criteria)

– Report (written) must include at least resident’s name, relevant drug, and irregularity – Must be sent to attending, director of nursing, and medical director, who must act on said report

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Phase 1 – §483.45 Pharmacy Services

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  • Attending must document in medical record

that identified irregularity was reviewed and what, if any, action taken. If no changes, must document rationale

  • P&P for the monthly DRR should include:

– Time frames for steps in process – Steps pharmacist must take when he/she identifies an irregularity that requires urgent action to protect the resident

  • Within the first year, resident admitted on an

antipsychotic medication or after the facility has initiated an antipsychotic medication, the facility must attempt a GDR in two separate quarters (with at least one month between the attempts), unless clinically contraindicated.

  • After the first year, a GDR must be attempted

annually, unless clinically contraindicated

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Gradual Dose Reduction

Considerations Specific to Antipsychotics

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Gradual Dose Reduction

Considerations Specific to Antipsychotics

  • If resident has dementia and receives an

antipsychotic medication to treat behavioral symptoms, the GDR may be considered clinically contraindicated if:

– Resident’s target symptoms returned or worsened after the most recent attempt at a GDR within the facility; and – Physician documented rationale for why any additional attempted dose reduction at that time would be likely to impair the resident’s function or increase distressed behavior

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  • For resident receiving an antipsychotic to treat a psychiatric

disorder (e.g., schizophrenia, bipolar mania, or depression with psychotic features), GDR may be considered contraindicated, if: – Continued use follows standards of practice

  • r

– Resident’s target symptoms returned or worsened after most recent GDR attempt and – Physician documented rationale for why any additional attempted dose reduction would likely impair resident’s function or cause psychiatric instability by exacerbating an underlying medical or psychiatric disorder

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Gradual Dose Reduction

Considerations Specific to Antipsychotics

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Phase 2 - §483.45 Pharmacy Services

  • Definition of psychotropic medication – any

drug that affects brain activities associated with mental processes and behavior

  • Includes, but not limited to:

– Antipsychotics – Anti-anxieties – Antidepressants – Hypnotics

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Phase 2 - §483.45 Pharmacy Services

§483.45(e) Psychotropic Drugs. [§483.45(e)(1)-(5) will be implemented beginning November 28, 2017 (Phase 2)]

  • Based on a comprehensive assessment of a

resident, the facility must ensure that--

1) Residents who have not used psychotropic drugs are not given these drugs unless the medication is necessary to treat a specific condition as diagnosed and documented in the clinical record; 2) Residents who use psychotropic drugs receive gradual dose reductions, and behavioral interventions, unless clinically contraindicated, in an effort to discontinue these drugs;

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Phase 2 - §483.45 Pharmacy Services

3) Residents do not receive psychotropic drugs based on a PRN order unless that medication is necessary to treat a diagnosed specific condition that is documented in the clinical record; and 4) PRN orders for psychotropic drugs are limited to 14 days. Except if attending physician or prescribing practitioner believes that it is appropriate for the PRN order to be extended beyond 14 days; he/she should document rationale in the resident’s medical record and indicate the duration for the PRN order 5) PRN orders for antipsychotic drugs are limited to 14 days and cannot be renewed unless the attending physician or prescribing practitioner evaluates the resident for the appropriateness of that medication

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More New MDS Items – 10/1/17

  • Changed Section P title from Restraints to

Restraints and Alarms

  • Physical Restraints P0100.

– Definition of Physical restraint unchanged – Physical restraints are any manual method or physical or mechanical device, material or equipment attached or adjacent to the resident's body that the individual cannot remove easily which restricts freedom of movement or normal access to one's body.

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P0200 Alarms

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An alarm is any physical or electronic device that monitors resident movement and alerts the staff when movement is detected.

Coding:

  • 0. Not used
  • 1. Used less than daily
  • 2. Used daily

Enter codes in Boxes

  • A. Bed alarm
  • B. Chair alarm
  • C. Floor mat alarm
  • D. Motion sensor alarm
  • E. Wander/elopement alarm
  • F. Other alarm

When Completed?

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Interpretive Guidelines

F222 Restraints (continued)

  • Facility must design its

interventions not only to minimize the medical symptom, but also to address any underlying problems.

  • Interventions the facility

might incorporate into care planning: – Equipping the resident with a device that monitors his/her attempts to rise

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F222 Restraints

Right to be free from any restraint imposed for discipline

  • r convenience.

Definitions: “Convenience” is defined as any action taken by the facility to control a resident’s behavior

  • r manage a resident’s

behavior with a lesser amount

  • f effort by the facility and not

in the resident’s best interest

Interpretive Guidelines

F252 Environment

  • “Homelike environment” –

de-emphasizes institutional character of the setting….

  • The intent of the word

“homelike” in this regulations is that the NH should provide an environment as close to that of a private home

  • Good practices include the

elimination of: – Widespread and long- term use of chair and bed alarms

F309 Quality of Care

  • B. Cause Identification/Diagnosis

If medical causes of behaviors ruled out as root cause, facility should conduct systematic analysis and consideration of possible causes, including but not limited to:

  • Environmental factors, for

example noise levels that could cause misinterpretation of noises, such as… alarms

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Interpretive Guidelines

F323 Accidents

SUPERVISION is an intervention and means of mitigating accident risk. Adequate supervision may very from resident to resident and from time to time for the same resident. Tools or items, such as personal alarms can help monitor a resident’s activities, but do not eliminate the need for adequate supervision

Think about:

  • OBRA = helping residents attain

highest level of function

  • Dignity; making choices
  • Personal alarms sound at 90-

100 decibels – similar to lawnmower starting

  • Same negative consequences

as restraints – encourages resident NOT to move, sit still; loss of mobility, increased weakness, skin issues.

  • Not shown to reduce falls

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Reducing Personal Alarms

  • Person-centered care is our new driving focus

requiring significant change in clinical practices

  • Start with education – for the resident, family and staff
  • Consistent staffing and sticking to it
  • Create culture supporting safety through teamwork,

education, communication, compliance with protocols, feedback, management support, resident safety as a priority, and non-punitive response to mistakes

  • Care systems to allow residents to sleep through the

night – individualized care at night. Sleep hygiene programs do work!!

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Reducing Personal Alarms

  • “Listen” to environment – Empira, Minnesota consortium

in a 3-year grant program studying falls, found that noise was a major environmental factor contributing to falls – reduce noise = a reduction in falls

  • Hourly rounding – no chairs in nursing stations
  • Residents do NOT like (privacy)

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Staff conversations (night shift) TVs Hearing linked to balance – increases fall risk if trying to orient self Telephones Radios Personal alarms – same decibels as lawnmower, motorcycle start

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Remember to keep checking the website for more helpful information and events

AANAC Conference in St. Louis – May 3-5, 2017

Thank you for your participation!!

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Resources

  • Federal Register Final Rule

– https://www.federalregister.gov/documents/2016/10/04/ 2016-23503/medicare-and-medicaid-programs-reform-of- requirements-for-long-term-care-facilities

  • RAI User’s Manual

– https://www.cms.gov/Medicare/Quality-Initiatives- Patient-Assessment- Instruments/NursinghomeQualityInits/MDS30RAIManual. html

  • MDS 3.0 Technical Information

– https://www.cms.gov/medicare/quality-initiatives- patient-assessment- instruments/nursinghomequalityinits/nhqimds30technical information.html

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Resources

  • Checklist for prescribing opioids for chronic pain. US

Department of Health and Human Services, Centers for Disease Control and Preventions (CDC), March 2016.

https://www.cdc.gov/drugoverdose/pdf/pdo_checklist-a.pdf

  • Advance Copy of SOM with current F-Tags

https://www.cms.gov/Medicare/Provider-Enrollment-and- Certification/SurveyCertificationGenInfo/Downloads/Survey- and-Cert-Letter-17-07.pdf

  • Antipsychotic Medication Use Data Report. Source:

CMS Quality Measure, based on MDS 3.0 data

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Resources

  • “Rethinking the Use of Personal Change Alarms,”

Quality Partners of Rhode Island, state Quality Improvement Organizations, under contract with CMS, 2007

  • Pioneer Network – Promoting Mobility, Reducing

Falls and Alarms.

www.pioneernetwork.net/Providers/StarterToolkit/Step2/ Mobility

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