Carediscovery quality measures –release v
CareDiscovery Quality Measures –Release v9.2
Holly Lockwood, Product Support, BSN, MBA
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Release date will be Monday June 20, 2016
Aligns with the National Hospital Inpatient Quality Reporting
Measures Specifications Manual v5.1 discharges from 07-01-16 (3Q16) through 12-31-16 (4Q16)
Aligns with the specification manual for OP v9.0 For use in submitting
data for encounters from 01/01/16 through 06/30/16.
Specifications Manual for Joint Commission National Quality
Measures (v2016A-1) Discharges 07-01-16 (3Q16) through 12-31-16 (4Q16)
CDQM users must review the specifications manuals and IPPS/OPPS
Final rules. Slides are current as of June 9, 2016.
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OP measure changes (none)
IP measure changes
Appendix Changes
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OQR Program Changes
Not a lot of OP changes for July
OP-Web – OP-33 measure - External Beam Radiotherapy (EBRT) for
Bone Metastases – abstraction begins with January 1, 2016 discharges. Eight data elements (already available)
Hospitals will self-report OP-33 via the CMS web based tool annually
starting in 2017.
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External Beam Radiotherapy for Bone Metastases
OP – 33, Web-Based
Description: Percentage of patients, regardless of age, with a
diagnosis of painful bone metastases and no history of previous radiation who receive EBRT with an acceptable fractionation scheme.
Numerator Statement: All patients with painful bone metastases,
and no previous radiation to the same anatomic site who receive EBRT with any of the following recommended fractionation schemes: 30Gy/10fxns, 24Gy/6fxns, 20Gy/5fxns, and 8Gy/1fxn. The data for the numerator may be found in the consultation and office visit notes, outpatient treatment center record, and problem/diagnosis list.
Denominator Statement: All patients with painful bone metastases
and no previous radiation to the same anatomic site who receive EBRT. The data for the denominator may be found in the consultation and office visit notes, outpatient treatment center record, and other-treatment summaries.
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External Beam Radiotherapy for Bone Metastases
OP – 33, Web-Based
Denominator Criteria (Eligible Cases): All patients, regardless of
age & Bone metastases diagnosis (ICD-10-CM): C79.51, C79.52
AND CPT or HCPCS: 77261, 77262, 77263
Denominator Exclusions:
Documentation of medical reason(s) including: Previous radiation treatment to the same anatomic site Patients with femoral axis cortical involvement greater than 3 cm in
Patients who have undergone a surgical stabilization procedure Patients with spinal cord compression, cauda equina compression, or
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External Beam Radiotherapy for Bone Metastases
OP – 33, Web-Based
OP EBRT Measure Data
See CMS Fact Sheets for additional guidance
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Highlighted Inpatient Changes by Measure Set
SEP (12 - 48)
Global –ED/IMM (49-50)
VTE (51 – 54)
STK (55 - 70)
SUB/TOB (73 - 84)
PC & HBIPS (85 - 94)
IPF PPS (95 – 98)
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Highlighted Inpatient Changes by Measure Set
Removed AMI, SCIP, CAC, VTE 1,2,3, STK 1,2,3,5,6,8,10, IMM-1
with 1/1/16 discharges. VTE no VTE removed after 4Q15 dc's. Algorithm, MIF, Initial Population, Sampling section changes
VTE-5 & 6 new reference added based on the environmental scan.
STK 4 updates the selected reference for FDA labeling instructions.
Change data element name from: Administrative Contraindication
to Care to: Administrative Contraindication to Care, Severe Sepsis, Administrative Contraindication to Care, Septic Shock
Added new data elements for Septic Shock: Initial Hypotension &
Documentation of Septic Shock
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MIF Changes IP
SEP 1 –many changes due to data elements being removed and
added. Changes to MIF, algorithm, etc.
TOB-1, 2 & 3 - Denominator exclusion was changed from =< 3 days
length of stay to =< 1 day length of stay to increase the denominator population. The time frame to complete the tobacco use screen was changed based on recommendations from TOB Advisory Panel
Numerator Statement Change to: The number of patients who were
screened for tobacco use status within the first day of admission.
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Release Note supplement v5.1 out 4-14-16 – SEP-1
Rationale: A supplement to the Release Notes to include verbiage
that was omitted from original Release Notes
Description of Changes: SEP-1 Algorithm:
Change first Discharge Disposition right branch to "= 1, 2, 3, 4, 5, 6, 7"
and branch continuing down to "= 8."
Change calculation to "Sepsis Discharge Time (in minutes) = Discharge
Date and Discharge Time – Severe Sepsis Presentation Date and Severe Sepsis Presentation Time" and the following decision box to "Sepsis Discharge Time."
Change second Discharge Disposition right branch to "= 1, 2, 3, 4, 5, 6,
7" and branch continuing down to "= 8."
Change calculation to "Shock Discharge Time (in minutes) = Discharge
Date and Discharge Time – Septic Shock Presentation Date and Septic Shock Presentation Time" and the following decision box to "Shock Discharge Time."
Specifications Manual for National Hospital Inpatient Quality Measures Discharges 07-01-2016 (3Q16) through 12-31-16 (4Q16)
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Administrative Contraindication to Care, Septic Shock
(SEP-1)
Definition: Documentation of refusal of blood draw, fluid
administration, or vasopressor administration prior to or within 6 hours
following presentation of septic shock.
Suggested Data Collection Question: Did the patient or surrogate
decision-maker decline consent for blood draw, fluid administration, or
vasopressor administration prior to or within 6 hours following
presentation of septic shock?
1 (Yes) There is documentation by a physician/APN/PA that the patient
or decision-maker has refused either blood draw, fluid administration, or vasopressor administration prior to or within 6 hours following presentation of septic shock.
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Administrative Contraindication to Care, Septic Shock
(SEP-1)
Allowable Values Continued:
2 (Yes) There is a witnessed consent form for either blood draw, fluid
administration, or vasopressor administration that is marked "refused" prior to or within 6 hours following presentation of septic shock.
3 (No) There is no physician/APN/PA documentation or witnessed
consent form that the patient or decision-maker has refused either blood draw, fluid administration, or vasopressor administration prior to or within 6 hours following presentation of septic shock.
Notes for Abstraction: Only acceptable sources are
physician/APN/PA documentation or a witness- signed consent form
marked "refused."
• Consent forms either signed or unsigned by the patient or decision-maker that are marked "refused" and witnessed by a physician, APN, PA or other hospital personnel, are acceptable.
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Administrative Contraindication to Care, Septic Shock
(SEP-1)
Notes for Abstraction: Documentation of refusal of blood draw, fluid
administration, or vasopressor administration that is present prior to or
within 6 hours following presentation of septic shock can be used.
Sources: Consultation reports, H&P, Physician/APN/PA notes &
Witnessed consent forms
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Administrative Contraindication to Care, Severe Sepsis
(SEP 1)
Definition, Question and Allowable Values –Add the language "prior
to or within 6 hours following presentation of severe sepsis?" at the
end.
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Broad Spectrum or Other Antibiotic Administration
Selection (SEP-1)
Notes for Abstraction Changes:
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Broad Spectrum or Other Antibiotic Administration
Time (SEP-1)
Notes for Abstraction Changes:
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Capillary Refill Examination Date & Time (SEP-1)
Definition, Question and Notes for Abstraction Changes:
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Capillary Refill Examination Performed (SEP-1)
Question and Notes for Abstraction Changes:
Inclusions: Add Peripheral perfusion
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Cardiopulmonary Evaluation Date, Performed & Time
(SEP-1)
Cardiopulmonary Evaluation Date had Definition, Question and
Notes Changes add word documented:
Cardiopulmonary Evaluation Performed Changes:
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Central Venous Oxygen Measurement, Date & Time
(SEP-1)
Definition, Values and Notes for Abstraction Changes:
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Central Venous Oxygen Measurement, Date & TIME
(SEP-1)
Definition, Values and Notes for Abstraction Changes & add VS
flow sheet to sources for CVO Measurement Time
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Crystalloid Fluid Administration (SEP-1)
Definition and Question Changes:
Allowable Value Changes:
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Crystalloid Fluid Administration (SEP-1)
Notes For Abstraction Changes:
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Crystalloid Fluid Administration (SEP-1)
Notes For Abstraction Changes & additional Sources:
Inclusions Add:
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Crystalloid Fluid Administration Date & Time (SEP-1)
Definition and Question Changes
Notes For Abstraction Changes:
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Directive for Comfort Care or Palliative Care, Septic
Shock & Directive for Comfort Care or Palliative Care,
Severe Sepsis (SEP-1)
Definition Change to Add a section- Palliative Care is the
identification, prevention, and treatment of suffering by means of
assessment of the physical, psychosocial, intellectual, and spiritual
needs of the patient with a goal of supporting and optimizing the
patient's quality of life. Palliative care ensures a partnership between
practitioner, patient, and family to provide support in decision making at
any stage in the patient's care.
Allowable Value Changes:
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Directive for Comfort Care or Palliative Care, Septic
Shock (SEP-1)
Notes for Abstraction Changes:
Inclusion Guidelines for Abstraction add new bullet:
Palliative care
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Documentation of Septic Shock (SEP 1)
Definition & Question:
Allowable Values and Notes for Abstraction:
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Initial Hypotension (SEP 1)
Definition & Question:
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Initial Lactate Level Collection, Date (SEP-1)
Inclusion Guidelines for Abstraction Changes (collection and
Date) :
Initial Lactate Level Collection Date/Time Notes changes:
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Initial Lactate Level Collection Result (SEP-1)
Notes for Abstraction Changes:
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Passive Leg Raise Exam Date & Time (SEP-1)
Question Change:
Notes for Abstraction Changes:
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Passive Leg Raise Exam Date (SEP-1)
Question Change:
Allowable Value Changes:
Notes for Abstraction Changes:
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Peripheral Pulse Evaluation Date (SEP-1)
Definition and Question changes similar to prior slides:
Notes for Abstraction Changes:
Change in second bullet: ‘must' to ‘may' Change in third bullet: ‘done' to ‘documented'
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Peripheral Pulse Evaluation Performed (SEP-1)
Question changes similar to prior slides:
Allowable Value Changes:
Notes for Abstraction: inserted word Documented
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Peripheral Pulse Evaluation Time (SEP-1)
Definition and Question changes:
Notes for Abstraction Changes:
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Allowable Value Changes (not to value 4):
Notes for Abstraction Changes:
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Repeat Lactate Level Collection, Date & Time (SEP-1)
Notes for Abstraction Changes:
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Septic Shock Present (SEP-1)
Notes for Abstraction Changes
Inclusions Guidelines for Abstraction Changes:
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Septic Shock Presentation Date, Time (SEP-1)
Notes for Abstraction Changes:
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Severe Sepsis Present (SEP-1)
Notes for Abstraction Changes:
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Skin Examination Date, Performed, Time (SEP-1)
Definition and Question had clarifying language added:
Notes for Abstraction Changes (Date& Time):
Inclusions for Abstraction Skin Exam Performed: add Mottled
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Vasopressor Administration, Date, Time (SEP-1)
Allowable Value Changes:
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Vasopressor Administration, Date, Time (SEP-1)
Notes for Abstraction Changes:
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Vital Signs Performed (SEP-1)
Clarifies the requirements for the vital signs review
Notes for Abstraction Changes to the second bullet:
Vital signs review is done to assess overall status. The review
must include temperature, pulse (also referred to as heart rate), respirations, and systolic and diastolic blood pressure reading.
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Arrival Date & Time (ED-1, STK-4)
Notes for Abstraction Changes: add sub bullet and changes to 6th
bullet shown at bottom
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Influenza Vaccination Status (IMM-2)
Notes for Abstraction Changes:
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Reason for No Administration of VTE Prophylaxis (VTE-
6)
Definition, Question and Allowable Value add pharmacist:
Exclusion Guidelines for Abstraction Changes:
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VTE Confirmed (VTE-5,6)
Notes for Abstraction Changes:
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VTE Diagnostic Test (VTE 5,6)
Inclusion Guidelines for Abstraction: Diagnostic testing includes
the following: THIS LIST IS ALL INCLUSIVE
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VTE Prophylaxis Status (VTE 6)
Notes for Abstraction Changes:
Inclusion Guidelines for Abstraction:
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STK Changes
Adding STK to the TJC manual –changes throughout
STK 6 had MIF and algorithm changes.
Removal of Aspirin(9) and GCS(4) from VTE Prophylaxis. See notes
for changes to these data elements.
References have been updated to reflect current evidence. (tPA, etc.)
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Arrival Date & Time (STK records)
Notes for Abstraction Changes Date:
Notes for Abstraction Changes Time:
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STK Data Element Changes
Antithrombotic Therapy Administered by End of Hospital Day 2
Atrial Fibrillation/Flutter- Removed an exception that not longer
Date Last Known Well – added to code stroke forms to inclusions
and modified exclusions to Stroke Education Form & Core Measure Form
Education Addresses Activation of Emergency Medical System-
Notes changes Educational material must address activation of the emergency medical system (EMS) if signs or symptoms of stroke or transient ischemic attack (TIA) occur.
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Date Last Known Well (STK 4)
Inclusion Guidelines for Abstraction -Add Code STK Form
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STK Data Element –Education (STK 8)
Education Addresses Follow-up After Discharge- Notes changes
If it does not include STK follow up = No Educational material must address follow-up after discharge If documentation reflects that educational material regarding follow-up
after discharge was given to the patient/caregiver, select "Yes", even if a copy of the material is not present
Education Addresses Medication Prescribed at Discharge -
Abstraction is a two-step process:
1. Compile a list of all of the medications being prescribed at discharge,
based on available medical record documentation.
2. Check list of discharge medications against the written discharge
instructions given to ensure that the discharge instructions addressed all of the discharge meds prescribed.
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STK Data Element –Education (STK 8)
Education Addresses Risk Factors for Stroke- Individual risk
factors that are not mentioned in the context of education provided on the risk factors for stroke, do not count.
Educational material which addresses risk factors for transient ischemic
attack (TIA) is acceptable.
Education Addresses Warning Signs and Symptoms of Stroke-
Educational material must address what to do if warning signs or symptoms of stroke or transient ischemic attack (TIA) are noted.
If the medical record contains documentation of education that does not
include stroke and warning signs and symptoms, select "No
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STK Data Element Changes
Elective Carotid Intervention - When documentation indicates that
the carotid intervention is elective admitting orders to obtain informed consent for a carotid procedure; pre-operative testing completed prior to admission; surgical orders for carotid endarterectomy dated prior to arrival select "Yes."
If sent by the physician or transferred for intervention select yes.
IV OR IA Thrombolytic (t-PA) Therapy Administered at This
Hospital or Within 24 Hours Prior to Arrival- Notes changed
If there is documentation that the patient received IV or IA thrombolytic (t-
PA) therapy and mechanical thrombectomy at this hospital or within 24 hours prior to arrival, select "Yes."
If there is documentation that the patient received mechanical
thrombectomy only with no IV or IA thrombolytic (t-PA) given, select "No."
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Elective Carotid Intervention (STK-4)
Notes for Abstraction Changes:
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STK Data Element Changes
Last Known Well- Select "Yes" if BOTH a date and time Last Known
Well are documented. Select "No" if there is ANY physician/APN/PA documentation that Last Known Well is "UNKNOWN."
If the Time Last Known Well is clearly greater than 2 hours prior to
hospital arrival AND no time is documented, select "No."
Reason for Extending the Initiation of IV Thrombolytic – added to
notes that If "other" reasons are not mentioned in the context of IV thrombolytics, do not make inferences. Added examples and changes to Exclusion Guidelines.
Reason for No VTE Prophylaxis – Hospital Admission - Updated
flow of bullets in notes. Added new sub bullet- "No VTE Prophylaxis", "No VTE Prophylaxis needed" [no reason given].
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STK Data Element Changes
Reason for Not Administering Antithrombotic Therapy by End of
Hospital Day 2 – Definition changed to: Reason for not
administering antithrombotic therapy by end of hospital day 2.
Other reasons documented by physician/APN/PA or pharmacist.
Notes Changes: documentation of a hold on antithrombotics or
discontinuation that occurs the day of or day after hospital arrival constitutes a "clearly implied" reason for not administering antithrombotic therapy by end of hospital day 2. A hold/discontinuation of all P.O. medications counts if an antithrombotic was on order at the time of the notation. NPO is NOT a reason for not administering antithrombotic therapy without explicit documentation that no antithrombotic medication should be given.
Refer to Appendix C, Table 8.2 do not use T 2.6
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Reason for Extending the Initiation of IV Thrombolytic
(STK-4)
Notes for Abstraction Changes: Added Examples
Exclusion Guidelines for Abstraction Changes:
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Reason for Not Initiating IV Thrombolytic (STK-4)
Definition & Notes Changes to add language:
Notes for Abstraction Changes: "other" reasons are not mentioned
in the context of IV thrombolytics, do not make inferences below are
unacceptable ex. to select no:
Exclusion Guidelines for Abstraction add: Delay in hospital arrival
greater than 2 hours
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Reason for Not Prescribing
Antithrombotic/Anticoagulation Therapy at Discharge
(STK 2 & 3)
Reason for Not Prescribing Antithrombotic/Anticoagulation
Therapy at Discharge –Definition Remove: Hemorrhagic stroke
Notes for Abstraction -Reasons for not prescribing antithrombotic
therapy at hospital discharge must be documented with one exception: Patient/family refusal of any form of antithrombotic therapy (e.g., "ASA refused," "Patient refusing antithrombotic therapy") may be documented by a nurse.
Inclusion Guidelines: None Refer to Appendix C, Table 8.2
Exclusion Guidelines: Antithrombotic medication allergy described
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Reason for Oral Factor Xa Inhibitor (STK 1)
Change is to accept pharmacist documentation for the reason for Oral
Factor Xa Inhibitor.
Question Change:
Notes for Abstraction Change: The only acceptable reasons are
identified in the list of inclusions. No other reasons will be accepted
Suggested Data Sources Change "PA" to "PA or PHARMACIST"
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Time Last Known Well (STK-4)
Notes for Abstraction Changes:
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Time Last Known Well (STK-4)
Notes for Abstraction Changes:
Exclusions:
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Appendix A Changes
Appendix A & C table changes due to measure sets being removed
Appendix A & C tables designated as "Reserved for Future Use" and
"Retired" are being removed to simplify the index.
Table 8.3: Carotid Intervention Procedures adds ICD-10-PCS codes
equivalent to ICD-9-CM procedure code 39.22 aortic-subclavian-carotid-bypass. Add several
Table 12.9: Influenza will remove the use of ICD-10 codes that are
non-specific to influenza vaccination.
Table 13.1: Alcohol Dependence remove several codes as they do not
reflect a current alcohol use or substance use disorder.
Table 13.2: Drug Dependence remove F1921 Other psychoactive
substance dependence, in remission
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Appendix C Medication Table Changes
Table 5.0 - Antibiotic Monotherapy, Sepsis revised to
remove Amoxicillin/clavulanate and Augmentin as it is only
available orally and the measure requires IV antibiotics.
remove Tequin and gatifloxacin since IV formulations have been
removed from the market due to safety reasons.
Table 5.1 - Antibiotic Generic/Trade Name Crosswalk, Sepsis revised
to add Cefotan and Cefotetan at the request of the measure steward.
Table 9.1: FDA-Approved Tobacco Cessation Medications
inadvertently left off the table have been added.
Nicorette lozenge Wellbutrin
Appendix H Updates Also- Table 2.1, T 2.3 & T 2.7
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Alcohol Use Status (all SUB)
Notes for Abstraction Changes:
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Alcohol Use Status (all SUB)
Notes for Abstraction Changes Continued:
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Brief Intervention (SUB-2)
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Brief Intervention (SUB-2)
Notes for Abstraction Changes:
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Tobacco Use Status (all TOB)
Allowable Value Changes:
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Tobacco Use Status (all TOB)
Notes for Abstraction Changes:
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Tobacco Use Status (all TOB)
Notes for Abstraction Changes:
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Prescription for Tobacco Cessation Medication (TOB-3
& 4)
Notes for Abstraction Changes:
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Reason for No Tobacco Cessation Medication at
Discharge (TOB-3) & During the Hospital Stay (TOB-2)
Notes for Abstraction Changes:
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Referral for Outpatient Tobacco Cessation Counseling
(TOB 3 & 4)
Notes for Abstraction Changes:
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Tobacco Use Treatment FDA-Approved Cessation
Medication (TOB-2)
Question & allowable values removed: "within the first three days
after admission"
Notes for Abstraction Changes:
Exclusion Guidelines: None
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Tobacco Use Treatment Practical Counseling (TOB-2)
Question & Allowable Values removed: "within the first three days
after admission"
Notes for Abstraction Changes:
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PC and HBIPS Changes
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Hospital-Based Inpatient Psychiatric Services (HBIPS) - retired
HBIPS-4, HBIPS-6 and HBIPS-7
Removed the word "Core" from the title of manual and other manual
sections as appropriate
Perinatal Care (PC) - removed clinical trial from all measures, and risk
adjustment from PC-02
The PDF updated Feb. 2016: A typographical error for Gestational
Age in the PC-03 algorithm picture has been corrected. The weeks value was revised from ">=24 and <32" to ">=24 and <34".
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Advanced Certification Heart Failure (ACHF) and Advanced
Certification Heart Failure Outpatient (ACHFOP) measure sets are added to the TJC Manual.
Stroke (STK) measure set is added to the TJC Manual-see prior
Sampling Sections: Remove all references to SCIP, AMI, and CAC
measure sets, and HBIPS-4, HBIPS-6 and HBIPS-7 measures. Include STK in the examples in the content as one of the measure sets presented in the manual.
The name of the manual changed from "Specifications Manual for
Joint Commission National Quality Core Measures" to "Specifications Manual for Joint Commission National Quality Measures."
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PC Changes
Clinical trial was removed to align with the eCQM version- algorithm &
other changes throughout.
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PC Data Element Changes
Admission to NICU- Clarification was added to address admissions
for observation.
Exclusive Breast Milk Feeding- Clarification added to help identify
actual feedings the newborn received in order to determine exclusive breast milk feeding. If the newborn received IV fluids this is the same as a medication and not a feeding. Sources changed.
Labor -Clarification was added for acceptable documentation for
labor. Notes changed to indicate documentation of labor should be abstracted at face value. Clarified documentation of regular contractions with or without cervical change.
Excluded- Prodromal is not an acceptable descriptor for labor
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PC Data Element Changes
Number of Previous Live Births -Clarification was added for using
parity from the EHR and use of GTPALGTPAL documentation alone does not indicate previous live births. Parity may be used for the number of previous deliveries resulting in a live birth if zero is documented. If parity in the EHR is "one" and includes delivery for the current hospitalization, abstract zero.
Term Newborn - notes added to determine if the newborn was term.
Gestational age should be rounded off to the nearest completed week, not the following week.
an infant born on the 5th day of the 36th week (35 weeks and 5/7 days)
is at a gestational age of 35 weeks, not 36 weeks.
In cases when there is conflicting documentation, e.g., both term and a
gestational age of 36 weeks are documented, the gestational age takes precedence.
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Patient Status at Discharge (HBIPS 5)
Definition: Documentation in the medical record of the patient's status
at the time the patient left the hospital-based inpatient psychiatric care
setting
Question: What was the patient's status at the time the patient left the
hospital-based inpatient psychiatric care setting?
Allowable Values:
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Patient Status at Discharge (HBIPS 5)
Notes for Abstraction, sources:
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HBIPS Data Element Changes
Appropriate Justification for Multiple Antipsychotic Medications-
Revisions were made to reflect the retirement of HBIPS-6 and HBIPS-7.
Number of Antipsychotic Medications Prescribed at Discharge –
Remove continuing care plan from sources
NEW: Patient Status at Discharge -added due to the retirement of
HBIPS-4, 6 and 7 and the removal of the data element Patient Referral to Next Level of Care Provider in order to exclude patients who were discharged from the psychiatric care setting
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Appendix A - ICD-10 & C (meds) Code Tables JC
Manual
Addition of STK measure set and tables to TJC Manual.
ICD-10-CM diagnosis codes were removed from Table 11.10.1 and
Table 11.10.2, since these codes are not specifically used to include or exclude cases from PC-04.
Appendix C – Medication Tables
Table 10.0 was updated to include new antipsychotic medications.
Appendix D- Glossary updates since measures sets removed from
CMS' Hospital Inpatient Quality Reporting program and The Joint Commission's Flexible ORYX® performance reporting requirements beginning with 1/1/2016 discharges.
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For facilities participating in the IPF-PPS program, note that 4Q 2015
IPF-PPS data (HBIPS/SUB/TOB) will be entered into QualityNet in July of 2016 tentatively, as this data is submitted annually and not quarterly.
CMS removed HBIPS 6 and HBIPS 7 & then adopted the two new
transition measures. (next slides)
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IPFQR Transition Measures & Changes
Transition Record measures & Metabolic Screening measure:
Inpatient Psychiatric Facilities (IPFs) were originally required to begin collecting these measures starting July 1, 2016.
The revised date for the beginning of measure collection is now January 1, 2017 and will apply to the Fiscal Year (FY) 2019 payment determination. IPFs will be required to report all four quarters of data or face a payment reduction. Reporting periods for all other measures remain unchanged.
There will be data elements: View the Inpatient Psychiatric Facilities
Program Manual for details.
Effective January 1, 2016, HBIPS-4, HBIPS-6 and HBIPS-7 were no
longer required by CMS or TJC.
Truven Health Analytics Inc. All Rights Reserved.
IPFQR Transition Measures
The Inpatient Psychiatric Facility Prospective Payment System (IPF-PPS) will be requiring three new chart abstracted measures to meet the CMS reporting requirements for the IPFQR Program.
These measures are:
Transition Record with Specified Data Elements - the percentage of
patients discharged from an IP facility, or caregivers, who received a transition record with specified elements at the time of discharge
Timely Transmission of Transition Record - -the percentage of patients
discharged from an inpatient facility for whom a transition record was transmitted to the health care setting designated for follow-up care within 24 hours of discharge.
Screening for Metabolic Disorders –awaiting further details from CMS
Truven Health Analytics Inc. All Rights Reserved.
Truven Health Analytics Inc. All Rights Reserved.
Truven Health Analytics Inc. All Rights Reserved.
New Functionality and Enhancements
Sepsis Sub-Measures – updated the Truven Sepsis sub-measures
to the new specifications for July discharges
Errors and Warnings – additional errors and warnings added to
Sepsis cases per CMS requirements
National Provider ID – NPI now required to be numeric only, error
will indicate if it has alpha characters as CMS now rejects cases with a non-numeric NPI
Expedite data loader – for clients using the Expedite module
improvements have been made to the tool that loads the HL7 data, due to this change only data from March 21, 2016 and forward will be available.
Truven Health Analytics Inc. All Rights Reserved.
Log on to Product Support Web Site
ill direct you to the
CareDiscovery Quality Measures Customer Portal.
Please see our Advantage Community for bulletins or notices at
Advantage Community -
For complete regulatory requirements, always refer to the appropriate specifications manuals according
to discharge dates published by CMS and TJC. It is your facility's responsibility to comply with core measures requirements as regulated by CMS and TJC. The specifications manuals are available via the resource tab of the CareDiscovery Quality Measures application under Resources.
Also you may reveal
the manual by clicking on the abstraction question within the CDQM application.
Analytics recommends that you examine the specifications manuals carefully when revised versions are published and determine how the changes may affect your facility.
Truven Health Analytics Inc. All Rights Reserved.
Truven Health Analytics Inc. All Rights Reserved.
Source: http://events-na7.adobeconnect.com/content/connect/c1/1153780968/en/events/event/private/1155984607/1651676287/event_landing/_jcr_content/par/download/file.res/CareDiscovery%20Quality%20Measures%20Release%20v9_2.pdf
Die Zeitung der KleintierKlinik Hannover Parvovirose – immer auch wenn die Welt heut- noch eine aktuelle zutage eine digitale ist und wir mit Nachrichten so-zusagen im Sekundentakt Erkrankung überfl utet werden, halten wir an unserer tie-risch gut! in Zeitungsform fest. Somit freuen wir uns, Sie wieder mit wichtigen Informationen zu Tieren und aus
International Journal of Behavioral Nutrition and Physical Activity ResearchWho will lose weight? A reexamination of predictors of weight loss in womenPedro J Teixeira*, António L Palmeira, Teresa L Branco, Sandra S Martins, Cláudia S Minderico, José T Barata, Analiza M Silva and Luís B Sardinha Address: Department of Exercise and Health, Faculty of Human Movement – Technical University of Lisbon, Cruz Quebrada, PORTUGAL