Core measures
Core measures are based on data received from your facility in the Core measures file. There are no additional calculations applied to the encounter-level values provided in that file. We are able to receive and display values for the following core measure sets:
- AMI (Acute Myocardial Infarction) core measures
- ASC (Ambulatory Surgery Center) quality measures
- CAC (Childrens' Asthma Care) performance measures
- ED (Emergency Department) measures
- HBIPS (Hospital-Based Inpatient Psychiatric Services) core measures
- HF (Heart Failure) core measures
- IMM (Immunization) core measures
- OP (Outpatient) core measures
- PC (Perinatal Care) core measures
- PN (Pneumonia) core measures
- SCIP (Surgical Care Improvement Project) core measures
- STK (Stroke) core measures
- SUB (Substance Abuse) core measures
- TOB (Tobacco Abuse) core measures
- VTE (Venous Thromboembolism) core measures
AMI (Acute Myocardial Infarction) core measures
Measure name |
Description |
Polarity |
All Payer benchmarks? |
Medicare benchmarks? |
Benchmark detail level |
---|---|---|---|---|---|
AMI Core Measure Bundle |
Acute myocardial infarction (AMI) patients which received all appropriate quality of care measures, including AMI-1 - Aspirin within 24 Hours, AMI-2 - Aspirin at Discharge, AMI-3 - ACE or ARB at Discharge, AMI-4 - Smoking Cessation, AMI-5 - Beta-Blocker at Discharge, AMI -10 - Statin Prescribed at Discharge |
High |
No |
No |
N/A |
AMI Overall |
Sum of Numerators for all AMI measures / Sum of Denominators for all AMI measures |
High |
No |
No |
N/A |
AMI-1 - Aspirin within 24 Hours |
Acute myocardial infarction (AMI) patients without aspirin contraindications who received aspirin within 24 hours before or after hospital arrival. |
High |
No |
No |
N/A |
AMI-2 - Aspirin at Discharge |
AMI patients without aspirin contraindications who were prescribed aspirin at hospital discharge. |
High |
No |
No |
N/A |
AMI-3 - ACE or ARB at Discharge |
AMI patients with left ventricular systolic dysfunction (LVSD) and without angiotensin converting enzyme inhibitor (ACE inhibitor) contraindications or angiotensin receptor blocker (ARB) contraindications who are prescribed an ACE inhibitor or an ARB at hospital discharge. |
High |
No |
No |
N/A |
AMI-4 - Smoking Cessation |
AMI patients with a history of smoking cigarettes, who are given smoking cessation advice or counseling during a hospital stay. |
High |
No |
No |
N/A |
AMI-5 - Beta-Blocker at Discharge |
AMI patients without beta-blocker contraindications who were prescribed a beta-blocker at hospital discharge. |
High |
No |
No |
N/A |
AMI-7a - Fibrinolytic Therapy within 30 Minutes |
AMI patients receiving fibrinolytic therapy during the hospital stay and having a time from hospital arrival to fibrinolysis of 30 minutes or less |
High |
No |
No |
N/A |
AMI-8a - PCI within 90 Minutes |
AMI patients receiving Percutaneous Coronary Intervention (PCI) during the hospital stay with a time from hospital arrival to PCI of 90 minutes or less. |
High |
No |
No |
N/A |
AMI -10 - Statin Prescribed at Discharge |
Acute myocardial infarction (AMI) patients, without statin contraindications, who are prescribed a statin at hospital discharge. For patients who had a heart attack and have high cholesterol, taking statins can lower the chance that they have another heart attack or die. |
High |
No |
No |
N/A |
ASC (Ambulatory Surgery Center) quality measures
Measure name |
Description |
Polarity |
All Payer benchmarks? |
Medicare benchmarks? |
Benchmark detail level |
---|---|---|---|---|---|
ASC-1 Patient Burn |
The number of discharges (patient encounters) who experience a burn prior to discharge from the ASC See the QualityNet website for more information. |
Low |
No |
No |
N/A |
ASC-2 Patient Fall |
The number of discharges (patient encounters) who experience a fall within the ASC See the QualityNet website for more information. |
Low |
No |
No |
N/A |
ASC-3 Wrong Site, Wrong Side, Wrong Patient, Wrong Procedure, Wrong Implant |
The number of discharges (patient encounters) who experience a wrong site, side, patient, procedure, or implant See the QualityNet website for more information. |
Low |
No |
No |
N/A |
ASC-4 Hospital Transfer/Admission |
The percentage of ASC admissions (patients) who are transferred or admitted to a hospital upon discharge from the ASC See the QualityNet website for more information. |
Low |
No |
No |
N/A |
ASC-5 Prophylactic Intravenous (IV) Antibiotic Timing |
Intravenous (IV) antibiotics given for prevention of surgical site infection were administered on time NOTE: Measures ASC-5, -6, and -7 have been removed from the program beginning with January 1, 2017 encounters. See the QualityNet website for more information. |
Low |
No |
No |
N/A |
ASC-6 Safe Surgery Checklist Use |
The use of a Safe Surgery Checklist for surgical procedures that includes safe surgery practices during each of the three critical perioperative periods: the period prior to the administration of anesthesia, the period prior to skin incision, and the period of closure of incision and prior to the patient leaving the operating room NOTE: Measures ASC-5, -6, and -7 have been removed from the program beginning with January 1, 2017 encounters. See the QualityNet website for more information. |
Low |
No |
No |
N/A |
ASC-7 ASC Facility Volume Data on Selected ASC Surgical Procedures |
The aggregate count of selected surgical procedures NOTE: Measures ASC-5, -6, and -7 have been removed from the program beginning with January 1, 2017 encounters. See the QualityNet website for more information. |
Low |
No |
No |
N/A |
ASC-8 Influenza Vaccination Coverage among Healthcare Personnel |
Percentage of Healthcare Personnel (HCP) who have received a flu vaccine. See the QualityNet website for more information. Facilities must report vaccination data for three categories of HCP: employees on payroll; licensed independent practitioners (who are physicians, advanced practice nurses, and physician assistants affiliated with the hospital but not on payroll); and students, trainees, and volunteers aged 18 or older. Show in Clinical Analytics only for personnel in the Physician Master File sent to Clinical Analytics. |
Low |
No |
No |
N/A |
ASC-9 Endoscopy/Polyp Surveillance: Appropriate Follow-up Interval for Normal Colonoscopy in Average Risk Patients |
Percentage of patients aged 50 to 75 years of age receiving a screening colonoscopy without biopsy or polypectomy who had a recommended follow-up interval of at least 10 years for repeat colonoscopy documented in their colonoscopy report See the QualityNet website for more information. |
Low |
No |
No |
N/A |
ASC-10 Endoscopy/Polyp Surveillance: Colonoscopy Interval for Patients with a History of Adenomatous Polyps - Avoidance of Inappropriate Use |
Percentage of patients aged 18 years and older receiving a surveillance colonoscopy, with a history of a prior colonic polyp(s) in previous colonoscopy findings, who had a follow-up interval of 3 or more years since their last colonoscopy See the QualityNet website for more information. |
Low |
No |
No |
N/A |
ASC-11 Cataracts - Improvement in Patient's Visual Function within 90 days Following Cataract Surgery |
Percentage of patients aged 18 years and older who had cataract surgery and had improvement in visual function achieved within 90 days following the cataract surgery, based on completing a pre-operative and post-operative visual function survey See the QualityNet website for more information. |
Low |
No |
No |
N/A |
ASC-12 Facility 7-Day Risk-Standardized Hospital Visit Rate after Outpatient Colonoscopy |
The measure estimates a facility-level rate of risk-standardized, all-cause, unplanned hospital visits within 7 days of an outpatient colonoscopy among Medicare Fee-for-Service (FFS) patients aged 65 years and older. See the QualityNet website for more information. |
Low |
No |
No |
N/A |
CAC (Childrens' Asthma Care) performance measures
Measure name |
Description |
Polarity |
All Payer benchmarks? |
Medicare benchmarks? |
Benchmark detail level |
---|---|---|---|---|---|
CAC Overall |
Sum of Numerators for all CAC measures/ Sum of Denominators for all CAC measures. |
High |
No |
No |
N/A |
CAC-1a - Relievers for Inpatient Asthma |
National guidelines recommend using reliever medication in the severe phase and gradually cutting down the dosage of medications to provide control of asthma symptoms. Relievers are medications that relax the bands of muscle surrounding the airways and are used to make breathing easier. |
High |
No |
No |
N/A |
CAC-2a - Systemic Corticosteroids |
National guidelines recommend using systemic corticosteroid medication (oral and IV medication that reduces inflammation and controls symptoms) in the severe phase and gradually cutting down the dosage of medications to provide control of the asthma symptoms. Systemic corticosteroids are a type of medication that works in the body as a whole. Systemic corticosteroids help control allergic reactions and reduce inflammation. |
High |
No |
No |
N/A |
CAC-3 - Home Management Plan of Care |
The Home Management Plan of Care document includes arrangements for follow-up care. It helps children with asthma and their caregivers develop a plan to manage the child’s asthma symptoms and to know when to take action. The plan of care should clearly tell the child and their caregiver when and how to use medication. |
High |
No |
No |
N/A |
ED (Emergency Department) measures
Measure name |
Description |
Polarity |
All Payer benchmarks? |
Medicare benchmarks? |
Benchmark detail level |
---|---|---|---|---|---|
ED-1 |
Average time, in minutes, from ED arrival to ED departure for patients admitted to the facility from the ED. Values are derived from your Core Measure Vendor File. NOTE: The core measure aggregation is a median time, but this software takes the arithmetic average when aggregating. There are 4 versions of this measure:
|
Low |
No |
No |
N/A |
ED-2 |
Average time, in minutes, from the admit decision time to ED departure time for patients admitted to the facility from the ED. Values are derived from your Core Measure Vendor File. NOTE: The core measure aggregation is a median time, but this software takes the arithmetic average when aggregating. There are 3 versions of this measure:
|
Low | No | No | N/A |
HBIPS (Hospital-Based Inpatient Psychiatric Services) core measures
Measure name |
Description |
Polarity |
All Payer benchmarks? |
Medicare benchmarks? |
Benchmark detail level |
---|---|---|---|---|---|
HBIPS-1 - Admission Screening |
Percent of all patients admitted to a hospital-based inpatient psychiatric setting who are screened within the first three days of admission for all of the following: risk of violence to self or others, substance use, psychological trauma history and patient strengths. Exclude: Patients for whom there is an inability to complete admission screening for Violence Risk, Substance Use, Psychological Trauma History and Patient Strengths within the first three days of admission and patients with a Length of Stay ≤ 3 days or ≥ 365 days. Values are derived from your Core Measure Vendor File. There are 5 versions of this measure:
|
High |
No |
No |
N/A |
HBIPS-2 - Physical Restraint |
The average number of hours that all patients admitted to a hospital-based inpatient psychiatric setting were maintained in physical restraint. Values are derived from your Core Measure Vendor File. There are 5 versions of this measure:
|
Low |
No |
No |
N/A |
HBIPS-3 - Seclusion |
The average number of hours that all patients admitted to a hospital-based inpatient psychiatric setting were held in seclusion. Values are derived from your Core Measure Vendor File. There are 5 versions of this measure:
|
Low |
No |
No |
N/A |
HBIPS-4 - Multiple Antipsychotic Medications at Discharge |
Percent of patients discharged from a hospital-based inpatient psychiatric setting on two or more antipsychotic medications. Values are derived from your Core Measure Vendor File. There are 5 versions of this measure:
|
Low |
No |
No |
N/A |
HBIPS-5 - Multiple Antipsychotic Medications at Discharge with Appropriate Justification |
Percent of patients discharged from a hospital-based inpatient psychiatric setting on two or more antipsychotic medications with appropriate justification. Exclude Patients who: expired, patients with an unplanned departure resulting in discharge due to elopement, patients with an unplanned departure resulting in discharge due to failing to return from leave, patients with a length of stay ≤ 3 days. Values are derived from your Core Measure Vendor File. There are 5 versions of this measure:
|
High |
No |
No |
N/A |
HBIPS-6 - Post Discharge Continuing Care Plan |
Percent of all patients discharged from a hospital-based inpatient psychiatric setting with a continuing care plan created. Exclude population: who expired, patients with an unplanned departure resulting in discharge due to elopement, patients or their guardians who refused aftercare, patients or guardians who refused to sign authorization to release information, patients with an unplanned departure resulting in discharge due to failing to return from leave. Values are derived from your Core Measure Vendor File. There are 5 versions of this measure:
|
High |
No |
No |
N/A |
HBIPS-7 - Post Discharge Continuing Care Plan Transmitted |
Percent of all patients discharged from a hospital-based inpatient psychiatric setting with a continuing care plan provided to the next level of care clinician or entity. Exclude population: who expired, patients with an unplanned departure resulting in discharge due to elopement, patients or their guardians who refused aftercare, patients or guardians who refused to sign authorization to release information, patients with an unplanned departure resulting in discharge due to failing to return from leave. Values are derived from your Core Measure Vendor File. There are 5 versions of this measure:
|
High | No | No | N/A |
HF (Heart Failure) core measures
Measure name |
Description |
Polarity |
All Payer benchmarks? |
Medicare benchmarks? |
Benchmark detail level |
---|---|---|---|---|---|
HF Core Measure Bundle |
Heart failure (HF) patients which received all appropriate quality of care measures, including: HF-1 - Discharge Instructions, HF-2 - LVS Function, HF-3 - ACE or ARB at Discharge, HF-4 - Smoking Cessation |
High |
No |
No |
N/A |
HF Overall |
Sum of Numerators for all CHF measures/ Sum of Denominators for all CHF measures |
High |
No |
No |
N/A |
HF-1 - Discharge Instructions |
Heart failure patients discharged home with written instructions or educational material given to patient or caregiver at discharge or during the hospital stay addressing all of the following: activity level, diet, discharge medications, follow-up appointment, weight monitoring, and what to do if symptoms worsen. |
High |
No |
No |
N/A |
HF-2 - LVS Function |
Heart failure patients with documentation in the hospital record that an evaluation of the left ventricular systolic (LVS) function was performed before arrival, during hospitalization, or is planned for after discharge. |
High |
No |
No |
N/A |
HF-3 - ACE or ARB at Discharge |
Heart failure patients with left ventricular systolic dysfunction (LVSD) and without angiotensin converting enzyme inhibitor (ACE inhibitor) contraindications or angiotensin receptor blocker (ARB) contraindications who are prescribed an ACE inhibitor or an ARB at hospital discharge. |
High |
No |
No |
N/A |
HF-4 - Smoking Cessation |
Heart failure patients with a history of smoking cigarettes, who are given smoking cessation advice or counseling during a hospital stay. |
High |
No |
No |
N/A |
IMM (Immunization) core measures
Measure name |
Description |
Polarity |
All Payer benchmarks? |
Medicare benchmarks? |
Benchmark detail level |
---|---|---|---|---|---|
IMM Core Measure Bundle |
Immunization (IMM) patients which received all appropriate quality of care measures, including IMM 1a and IMM 2 |
High |
No |
No |
N/A |
IMM Overall |
Sum of numerators for all IMM measures divided by the sum of denominators for all IMM measures |
High |
No |
No |
N/A |
IMM-1a - Pneumococcal Immunization - Overall Rate |
This prevention measure addresses acute care hospitalized inpatients 65 years of age and older (IMM-1b) and inpatients aged between 5 and 64 years (IMM-1c) who are considered high risk and were screened for receipt of pneumococcal vaccine and were vaccinated prior to discharge if indicated. The numerator captures two activities; screening and the intervention of vaccine administration when indicated. Patients who had documented contraindications to pneumococcal vaccine, patients who were offered and declined pneumococcal vaccine, and patients who received pneumococcal vaccine anytime in the past are captured as numerator events. |
High |
No |
No |
N/A |
IMM-1b - Pneumococcal Immunization - Age 65 and Older |
This prevention measure addresses acute care hospitalized inpatients 65 years of age and older who are considered high risk and were screened for receipt of pneumococcal vaccine and were vaccinated prior to discharge if indicated. The numerator captures two activities; screening and the intervention of vaccine administration when indicated. Patients who had documented contraindications to pneumococcal vaccine, patients who were offered and declined pneumococcal vaccine, and patients who received pneumococcal vaccine anytime in the past are captured as numerator events. |
High |
No |
No |
N/A |
IMM-1c - Pneumococcal Immunization - High Risk Populations (Age 5 through 64 years) |
This prevention measure address acute care hospitalized inpatients aged between 5 and 64 years who are considered high risk and were screened for receipt of pneumococcal vaccine and were vaccinated prior to discharge if indicated. The numerator captures two activities; screening and the intervention of vaccine administration when indicated. Patients who had documented contraindications to pneumococcal vaccine, patients who were offered and declined pneumococcal vaccine, and patients who received pneumococcal vaccine anytime in the past are captured as numerator events. |
High |
No |
No |
N/A |
IMM-2 - Influenza Immunization |
This prevention measure addresses acute care hospitalized inpatients age 6 months and older who were screened for seasonal influenza immunization status and were vaccinated prior to discharge if indicated. The numerator captures two activities: screening and the intervention of vaccine administration when indicated. Patients who had documented contraindications to the vaccine, patients who were offered and declined the vaccine, and patients who received the vaccine during the current year's influenza season but prior to the current hospitalization are captured as numerator events. |
High |
No |
No |
N/A |
OP (Outpatient) core measures
Measure name |
Description |
Polarity |
All Payer benchmarks? |
Medicare benchmarks? |
Benchmark detail level |
---|---|---|---|---|---|
OP 1 - Median Time to Fibrinolysis |
Median time from emergency department arrival to administration of fibrinolytic therapy in ED patients with ST-segment elevation or left bundle branch block on the ECG performed closest to ED arrival and prior to transfer. |
Low |
No |
No |
N/A |
OP 2 - Fibrinolytic Therapy within 30 Minutes |
Emergency Department AMI patients with ST-segment elevation or left bundle branch block on the ECG closest to arrival time receiving fibrinolytic therapy during the ED stay and having a time from ED arrival to fibrinolysis of 30 minutes or less. |
High |
No |
No |
N/A |
OP 3b - Median Time to Transfer to Another Facility for ACI |
Median time from emergency department arrival to time of transfer to another facility for acute coronary intervention |
Low |
No |
No |
N/A |
OP 4 - Aspirin at Arrival |
Emergency Department AMI patients or chest pain patients (with probable cardiac chest pain) who received aspirin within 24 hours before ED arrival or prior to transfer. |
High |
No |
No |
N/A |
OP 5 - Median Time to ECG |
Median time from emergency department arrival to ECG (performed in the ED prior to transfer) for AMI or chest pain patients (with probable cardiac chest pain). |
Low |
No |
No |
N/A |
OP 6 - Timing of Antibiotic Prophylaxis |
Surgical patients with prophylactic antibiotics initiated within one hour* prior to surgical incision.*Patients who received vancomycin or a fluoroquinolone for prophylaxis should have the antibiotic initiated within two hours prior to surgical incision. Due to the longer infusion time required for vancomycin or a fluoroquinolone, it is acceptable to start these antibiotics within two hours prior to incision time. |
High |
No |
No |
N/A |
OP 7 - Prophylactic Antibiotic Selection for Surgical Patients |
Surgical patients who received prophylactic antibiotics consistent with current guidelines (specific to each type of surgical procedure). |
High |
No |
No |
N/A |
OP - 8 MRI Lumbar Spine for Low Back Pain |
Percentage of MRI (Magnetic Resonance Imaging) of the Lumbar Spine studies with a diagnosis of low back pain on the imaging claim and for which the patient did not have prior claims-based evidence of antecedent conservative therapy See the QualityNet website for more information. |
High |
No |
No |
N/A |
OP - 9 Mammography Follow-Up Rates |
Percentage of patients with mammography screening studies that are followed by a diagnostic mammography, ultrasound, or Magnetic Resonance Imaging (MRI) of the breast in an outpatient or office setting within 45 days See the QualityNet website for more information. |
High |
No |
No |
N/A |
OP - 10 Abdomen CT Use of Contrast Material |
Percentage of abdomen studies that are performed with and without contrast out of all abdomen studies performed (those with contrast, those without contrast, and those with both) See the QualityNet website for more information. |
High |
No |
No |
N/A |
OP - 11 Thorax CT - Use of Contrast Material |
Percentage of thorax studies that are performed with and without contrast out of all thorax studies performed (those with contrast, those without contrast, and those with both) See the QualityNet website for more information. |
High |
No |
No |
N/A |
OP - 12 The Ability for Providers with HIT to Receive Laboratory Data Electronically Directly into their ONC-Certified EHR System as Discrete Searchable Data |
The extent to which a provider uses an Office of the National Coordinator for Health Information Technology (ONC) certified electronic health record (EHR) system that incorporates an electronic data interchange with one or more laboratories allowing for direct electronic transmission of laboratory data in the EHR as discrete searchable data elements See the QualityNet website for more information. |
High |
No |
No |
N/A |
OP - 13 Cardiac Imaging for Preoperative Risk Assessment for Non-Cardiac Low-Risk Surgery |
Percentage of Stress Echocardiography, Single Photon Emission Computed Tomography, Myocardial Perfusion Imaging (SPECT MPI), Cardiac Computed Tomography Angiography (CCTA), or Stress Magnetic Resonance Imaging (MRI) studies performed at a hospital outpatient facility in the 30 days prior to an ambulatory low-risk, non-cardiac surgery performed anywhere See the QualityNet website for more information. |
High |
No |
No |
N/A |
OP - 14 Simultaneous Use of Brain Computed Tomography (CT) and Sinus CT |
Percentage of Brain CT studies with a simultaneous Sinus CT (i.e., Brain and Sinus CT studies performed on the same day at the same facility) See the QualityNet website for more information. |
High |
No |
No |
N/A |
OP-15 Use of Brain Computed Tomography (CT) in the ED for Atraumatic Headache |
Percent of ED patients with atraumatic headache who are given a brain CT This measure was discontinued by CMS as of January 1, 2017 |
High |
No |
No |
N/A |
OP - 17 Tracking Clinical Results between Visits |
The extent to which a provider uses an Office of the National Coordinator for Health Information Technology (ONC) certified electronic health record (EHR) system to track pending laboratory tests, diagnostic studies (including common preventive screenings), or patient referrals See the QualityNet website for more information. |
High |
No |
No |
N/A |
OP-18a Median Time from ED Arrival to ED Departure for Discharged ED Patients - Overall Rate |
Median time from emergency department arrival to time of departure from the emergency room for patients discharged from the emergency department See the QualityNet website for more information. |
Low |
No |
No |
N/A |
OP-18b Median Time from ED Arrival to ED Departure for Discharged ED Patients - Reporting Measure |
Median time from emergency department arrival to time of departure from the emergency room for patients discharged from the emergency department See the QualityNet website for more information. |
Low |
No |
No |
N/A |
OP-18c Median Time from ED Arrival to ED Departure for Discharged ED Patients - Psychiatric/Mental Health Patients |
Median time from emergency department arrival to time of departure from the emergency room for patients discharged from the emergency department See the QualityNet website for more information. |
Low |
No |
No |
N/A |
OP-18d Median Time from ED Arrival to ED Departure for Discharged ED Patients - Transfer Patients |
Median time from emergency department arrival to time of departure from the emergency room for patients discharged from the emergency department See the QualityNet website for more information. |
Low |
No |
No |
N/A |
OP-20 Door to Diagnostic Evaluation by a Qualified Medical Personnel |
Median time from ED arrival to provider contact for Emergency Department patients See the QualityNet website for more information. |
Low |
No |
No |
N/A |
OP-21 Median Time to Pain Management for Long Bone Fracture |
Median time, in minutes, from emergency department arrival to time of initial oral, intranasal, or parenteral pain medication administration for emergency department patients with a principal diagnosis of long bone fracture |
Low |
No |
No |
N/A |
OP-22 - Left Without Being Seen |
Percent of patients who leave the Emergency Department (ED) without being evaluated by a physician/advanced practice nurse/physician’s assistant (physician/APN/PA) See the QualityNet website for more information. |
Low | No | No | N/A |
OP-23 Head CT or MRI Scan Results for Acute Ischemic Stroke or Hemorrhagic Stroke Patients who Received Head CT or MRI Scan Interpretation Within 45 Minutes of ED Arrival |
Emergency Department Acute Ischemic Stroke or Hemorrhagic Stroke patients who arrive at the ED within 2 hours of the onset of symptoms who have a head CT or MRI scan performed during the stay and having a time from ED arrival to interpretation of the Head CT or MRI scan within 45 minutes of arrival. |
Low |
No |
No |
N/A |
PC (Perinatal Care) core measures
Measure name |
Description |
Polarity |
All Payer benchmarks? |
Medicare benchmarks? |
Benchmark detail level |
---|---|---|---|---|---|
PC-01 - Elective Delivery |
Patients with elective vaginal deliveries or elective cesarean births at >= 37 and < 39 weeks of gestation completed See the Joint Commission website for more information. |
Low |
No |
No |
N/A |
PC-02 - Cesarean Section (CS) |
Nulliparous women with a term, singleton baby in a vertex position delivered by cesarean birth; See the Joint Commission website for more information. |
Low |
No |
No |
N/A |
PC-03 - Antenatal Steroids |
Patients at risk of preterm delivery at >=24 and <34 weeks gestation receiving antenatal steroids prior to delivering preterm newborns; count of patients with antenatal steroids initiated prior to delivering preterm newborns divided by patients delivering live preterm newborns with >=24 and <34 weeks gestation completed See the Joint Commission website for more information. |
High |
No |
No |
N/A |
PC-04 - HAC - Bloodstream Infections in Newborns |
Staphylococcal and gram negative septicemias or bacteremias in high-risk newborns; count of newborns with septicemia or bacteremia divided by count of live newborns See the Joint Commission website for more information. |
Low |
No |
No |
N/A |
PC-05 - Exclusive Breast Milk Feeding |
Exclusive breast milk feeding during the newborn's entire hospitalization; count of newborns that were fed breast milk only since birth divided by count of single term newborns discharged alive from the hospital See the Joint Commission website for more information. |
High |
No |
No |
N/A |
PC-05a - Exclusive Breast Milk Feeding considering mother's choice |
Exclusive breast milk feeding during the newborn's entire hospitalization, excluding those whose mothers chose not to breastfeed; count of newborns that were fed breast milk only since birth divided by count of single term newborns discharged alive from the hospital, excluding those who were, by choice, not breastfed. See the Joint Commission website for more information. |
High |
No |
No |
N/A |
PC-06 - Unexpected Complications in Term Newborns |
Unexpected complications among full term newborns with no preexisting conditions. See the Joint Commission website for more information. |
Low | No | No | N/A |
PC-06.0 Unexpected Complications in Term Newborns - Overall Rate |
(Severe Complications Numerator + Moderate Complications Numerator) x 1,000 Final Denominator |
Low | No | No | N/A |
PC-06.1 Unexpected Complications in Term Newborns - Severe Rate | Severe complications include neonatal death, transfer to another hospital for higher level of care, severe birth injuries such as intracranial hemorrhage or nerve injury, neurologic damage, severe respiratory and infectious complications such as sepsis. | Low | No | No |
N/A |
PC-06.2 Unexpected Complications in Term Newborns - Moderate Rate | Moderate complications include diagnoses or procedures that raise concern but at a lower level than the list for severe for example, use of CPAP or bone fracture. Examples include less severe respiratory complications for example, Transient Tachypnea of the Newborn, or infections with a longer length of stay not including sepsis, infants who have a prolonged length of stay of over 5 days. | Low | No | No | N/A |
PN (Pneumonia) core measures
Measure name |
Description |
Polarity |
All Payer benchmarks? |
Medicare benchmarks? |
Benchmark detail level |
---|---|---|---|---|---|
PN Core Measure Bundle |
Pneumonia (PN) patients which received all appropriate quality of care measures, including PN-2 - Pneumococcal Vaccine, PN-3b - Blood Culture, PN-4 - Smoking Cessation, PN-5c - Initial Antibiotic Timing, PN-6 - Initial Antibiotic Selection, PN-7 - Influenza Vaccination |
High |
No |
No |
N/A |
PN Overall |
Sum of numerators for all CAP measures / sum of denominators for all CAP measures |
High |
No |
No |
N/A |
PN-2 - Pneumococcal Vaccine |
Pneumonia inpatients age 65 and older who were screened for pneumococcal vaccine status and were administered the vaccine prior to discharge, if indicated. |
High |
No |
No |
N/A |
PN-3b - Blood Culture |
Pneumonia patients whose initial emergency room blood culture specimen was collected prior to first hospital dose of antibiotics. |
High |
No |
No |
N/A |
PN-4 - Smoking Cessation |
Pneumonia patients with a history of smoking cigarettes, who are given smoking cessation advice or counseling during a hospital stay. |
High |
No |
No |
N/A |
PN-5c - Initial Antibiotic Timing |
Pneumonia inpatients that receive within 6 hours after arrival at the hospital. Evidence shows better outcomes for administration times less than four hours. |
High |
No |
No |
N/A |
PN-6 - Initial Antibiotic Selection |
Immunocompetent patients with pneumonia who receive an initial antibiotic regimen that is consistent with current guidelines. |
High |
No |
No |
N/A |
PN-7 - Influenza Vaccination |
Pneumonia patients age 50 years and older, hospitalized during October, November, December, January, or February who were screened for influenza vaccine status and were vaccinated prior to discharge, if indicated. |
High |
No |
No |
N/A |
SCIP (Surgical Care Improvement Project) core measures
Measure name |
Description |
Polarity |
All Payer benchmarks? |
Medicare benchmarks? |
Benchmark detail level |
---|---|---|---|---|---|
SCIP Core Measure Bundle |
Surgery (SCIP) patients which received all appropriate quality of care measures, including SCIP-Inf -1a - Prophylactic Antibiotic, SCIP-Inf -2a - Antibiotic Selection, SCIP-Inf -3a - Antibiotic Discontinued, SCIP-Inf-6 - Appropriate Hair Removal, SCIP-Inf-9 - Urinary Catheter Removed, SCIP-Inf-10 - Perioperative Temperature Management, SCIP-VTE-1 - VTE Ordered, SCIP-VTE-2 - Appropriate VTE Therapy, SCIP-Card-2 - Beta-Blocker Therapy |
High |
No |
No |
N/A |
SCIP Overall |
Sum of Numerators for all SCIP measures / sum of denominators for all SCIP measures |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
SCIP-Card-2 - Beta-Blocker Therapy |
Surgery patients on beta-blocker therapy prior to arrival who received a beta-blocker during the perioperative period. The perioperative period for the SCIP cardiac measures is defined as 24 hours prior to surgical incision through discharge from post-anesthesia care/recovery area. |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
SCIP-Inf -1a - Prophylactic Antibiotic |
Surgical patients who received prophylactic antibiotics within 1 hour prior to surgical incision. |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
SCIP-Inf -2a - Antibiotic Selection |
Surgical patients who received the recommended antibiotics for their particular type of surgery. |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
SCIP-Inf -3a - Antibiotic Discontinued |
Surgical patients whose prophylactic antibiotics were discontinued within 24 hours after surgery end time. |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
SCIP-Inf-4 - Cardiac Patients Post-Op Blood Glucose |
Cardiac surgery patients with controlled 6 A.M. blood glucose (<200 mg/dL) on postoperative day one (POD 1) and postoperative day two (POD 2) with surgery end date being postoperative day zero (POD 0). |
High |
No |
No |
N/A |
SCIP-Inf-6 - Appropriate Hair Removal |
Surgery patients with appropriate surgical site hair removal. No hair removal or hair removal with clippers or depilatory is considered appropriate. Shaving is considered inappropriate. |
High |
No |
No |
N/A |
SCIP-Inf-9 - Urinary catheter removed on Postoperative Day 1 or Postoperative Day 2 with day of surgery being day zero |
Surgical patients with urinary catheter removed on Postoperative Day 1 or Postoperative Day 2 with day of surgery being day zero. |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
SCIP-Inf-10 - Surgery Patients with Perioperative Temperature Management |
Surgery patients for whom either active warming was used intraoperatively for the purpose of maintaining normothermia or who had at least one body temperature equal to or greater than 96.8° Fahrenheit/36° Celsius recorded within the 30 minutes immediately prior to or the 15 minutes immediately after Anesthesia End Time. |
High |
No |
No |
N/A |
SCIP-VTE-1 - VTE Ordered |
Surgery patients with recommended venous thromboembolism (VTE) prophylaxis ordered anytime from hospital arrival to 48 hours after surgery end time. |
High |
No |
No |
N/A |
SCIP-VTE-2 - Appropriate VTE Therapy |
Surgery patients who received appropriate venous thromboembolism (VTE) prophylaxis within 24 Hours prior to surgical incision time to 24 hours after surgery end time. |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
STK (Stroke) core measures
Measure name |
Description |
Polarity |
All Payer benchmarks? |
Medicare benchmarks? |
Benchmark detail level |
---|---|---|---|---|---|
STK Core Measure Bundle |
Stroke (STK) patients which received all appropriate quality of care measures, including STK-1, STK-2, STK-3, STK-4, STK-5, STK-6, STK-8, STK-10 |
High |
No |
No |
N/A |
STK Overall |
Sum of numerators for all STK measures/ sum of denominators for all STK measures |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
STK-1 - VTE Prophylaxis |
Ischemic and hemorrhagic stroke patients who received VTE prophylaxis or have documentation why no VTE prophylaxis was given the day of or the day after hospital admission See the Joint Commission website for more information. |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
STK-2 - Discharged on Antithrombotic Therapy |
Ischemic stroke patients prescribed antithrombotic therapy at hospital discharge See the Joint Commission website for more information. |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
STK-3 - Anticoagulant Therapy for Atrial Fibrillation/Flutter |
Ischemic stroke patients with atrial fibrillation/flutter who are prescribed anticoagulation therapy at hospital discharge. See the Joint Commission website for more information. |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
STK-4 - Thrombolytic Therapy |
Acute ischemic stroke patients who arrive at this hospital within 2 hours of the time they were last known to be well and for whom IV t-PA was initiated at this hospital within 3 hours of the time they were last known to be well. See the Joint Commission website for more information. |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
STK-5 - Antithrombotic Therapy |
Ischemic stroke patients administered antithrombotic therapy by the end of hospital day 2. See the Joint Commission website for more information. |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
STK-6 - Discharged on Statin Medication |
Ischemic stroke patients with LDL greater than or equal to 100 mg/dL, or LDL not measured, or who were on a lipid-lowering medication prior to hospital arrival are prescribed statin medication at hospital discharge. See the Joint Commission website for more information. |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
STK-8 - Stroke Education |
Ischemic or hemorrhagic stroke patients or their caregivers who were given educational materials during the hospital stay addressing all of the following: activation of emergency medical system, need for follow-up after discharge, medications prescribed at discharge, risk factors for stroke, and warning signs and symptoms of stroke. See the Joint Commission website for more information. |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
STK-10 - Assessed for Rehabilitation |
Percent of ischemic or hemorrhagic stroke patients who were assessed for rehabilitation services. Exclude population: less than 18 years of age, patients who have a Length of Stay greater than 120 days, patients with Comfort Measures Only documented, patients enrolled in clinical trials, patients admitted for Elective Carotid Intervention, patients discharged to another hospital, patients who left against medical advice, patients who expired, patients discharged to home for hospice care, and patients discharged to a health care facility for hospice care. Values are derived from your Core Measure Vendor File. See the Joint Commission website for more information. |
High |
No |
No |
N/A |
SUB (Substance Abuse) core measures
Measure name |
Description |
Polarity |
All Payer benchmarks? |
Medicare benchmarks? |
Benchmark detail level |
---|---|---|---|---|---|
SUB-2 - Alcohol Use Brief Intervention Provided or Offered |
Percentage of patients who screened positive for unhealthy alcohol use to whom a brief intervention was provided, offered or refused. Exclude: patients less than 18 years of age, patients who are cognitively impaired, patients who a have a duration of stay less than or equal to one day or greater than 120 days, patients with Comfort Measures Only documented. Values are derived from your Core Measure Vendor File. |
High |
No |
No |
N/A |
SUB-2a - Alcohol Use Brief Intervention Treatment |
Percent of patients who screened positive for unhealthy alcohol use, and did not refuse intervention, to whom a brief intervention was provided. Exclude: patients less than 18 years of age, patients who are cognitively impaired, patients who a have a duration of stay less than or equal to one day or greater than 120 days, patients with Comfort Measures Only documented. Values are derived from your Core Measure Vendor File. |
High |
No |
No |
N/A |
SUB-3 - Alcohol and Other Drug Use Disorder Treatment Provided or Offered at Discharge |
Percent of patients meeting the criteria for an alcohol or other drug use disorder who were provided or offered a prescription at discharge for medication for treatment of alcohol or drug use disorder OR a referral for addictions treatment. Exclude: patients less than 18 years of age, patient drinking at unhealthy levels who do not meet criteria for an alcohol use disorder, patients who are cognitively impaired, patients who expire, patients discharged to another hospital, patients who left against medical advice, patients discharged to another healthcare facility, patients discharged to home or another healthcare facility for hospice care, patients who have a length of stay less than or equal to three days or greater than 120 days, patients who do not reside in the United States, patients receiving Comfort Measures Only documented. Values are derived from your Core Measure Vendor File. |
High |
No |
No |
N/A |
SUB-3a - Alcohol and Other Drug Use Disorder Treatment at Discharge |
Percent of patients meeting the criteria for an alcohol or other drug use disorder who received a prescription at discharge for medication for treatment of alcohol or drug use disorder OR a referral for addictions treatment. Exclude: patients less than 18 years of age, patient drinking at unhealthy levels who do not meet criteria for an alcohol use disorder, patients who are cognitively impaired, patients who expire, patients discharged to another hospital, patients who left against medical advice, patients discharged to another healthcare facility, patients discharged to home or another healthcare facility for hospice care, patients who have a length of stay less than or equal to three days or greater than 120 days, patients who do not reside in the United States, patients receiving Comfort Measures Only documented. Values are derived from your Core Measure Vendor File. |
High |
No |
No |
N/A |
TOB (Tobacco Abuse) core measures
Measure name |
Description |
Polarity |
All Payer benchmarks? |
Medicare benchmarks? |
Benchmark detail level |
---|---|---|---|---|---|
TOB-2 - Tobacco Use Treatment Provided or Offered |
Percent of patients identified as tobacco product users within the past 30 days who received or refused practical counseling to quit AND received or refused FDA approved cessation medications during the hospital stay. Exclude patients who: less than 18 years of age, are cognitively impaired, have a duration of stay less than or equal to one day and greater than 120 days. Values are derived from your Core Measure Vendor File. |
High |
No |
No |
N/A |
TOB-2a - Tobacco Use Treatment |
Percent of patients identified as tobacco product users within the past 30 days who received counseling AND medication as well as those who received counseling and had reason for not receiving the medication. Exclude patients who: less than 18 years of age, are cognitively impaired, have a duration of stay less than or equal to one day and greater than 120 days. Values are derived from your Core Measure Vendor File. |
High |
No |
No |
N/A |
TOB-3 - Tobacco Use Treatment Provided or Offered at Discharge |
Percent of patients identified as tobacco product users within the past 30 days who were referred to or refused evidence-based outpatient counseling AND received or refused a prescription for FDA-approved cessation medication upon discharge. Exclude patients who: less than 18 years of age, are cognitively impaired, have a duration of stay less than or equal to one day and greater than 120 days. Values are derived from your Core Measure Vendor File. |
High |
No |
No |
N/A |
TOB-3a - Tobacco Use Treatment at Discharge |
Percent of patients identified as tobacco product users within the past 30 days who were referred to evidence-based outpatient counseling AND received a prescription for FDA-approved cessation medication upon discharge as well as those who were referred to outpatient counseling and had reason for not receiving a prescription for medication. Exclude patients who: less than 18 years of age, are cognitively impaired, have a duration of stay less than or equal to one day and greater than 120 days. Values are derived from your Core Measure Vendor File. |
High |
No |
No |
N/A |
VTE (Venous Thromboembolism) core measures
Measure name |
Description |
Polarity |
All Payer benchmarks? |
Medicare benchmarks? |
Benchmark detail level |
---|---|---|---|---|---|
VTE Core Measure Bundle |
Venous Thromboembolism (VTE ) patients which received all appropriate quality of care measures, including VTE-1, VTE-2, VTE-3, VTE-4, VTE-5, VTE-6 |
High |
No |
No |
N/A |
VTE Overall |
Sum of numerators for all VTE measures/ sum of denominators for all VTE measures |
High |
No |
No |
N/A |
VTE-1 - VTE Prophylaxis |
This measure assesses the number of patients who received VTE prophylaxis or have documentation why no VTE prophylaxis was given the day of or the day after hospital admission or surgery end date for surgeries that start the day of or the day after hospital admission. |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
VTE-2 - ICU VTE |
This measure assesses the number of patients who received VTE prophylaxis or have documentation why no VTE prophylaxis was given the day of or the day after the initial admission (or transfer) to the Intensive Care Unit (ICU) or surgery end date for surgeries that start the day of or the day after ICU admission (or transfer). |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
VTE-3 - Anticoagulation Overlap Therapy |
This measure assesses the number of patients diagnosed with confirmed VTE who received an overlap of parenteral intravenous or subcutaneous anticoagulation and warfarin therapy. For patients who received less than five days of overlap therapy, they should be discharged on both medications or have a reason for discontinuation of overlap therapy. Overlap therapy should be administered for at least five days with an international normalized ratio (INR) greater than or equal to 2 prior to discontinuation of the parenteral anticoagulation therapy, discharged on both medications or have a reason for discontinuation of overlap therapy. |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
VTE-4 - Heparin Therapy and Monitoring |
This measure assesses the number of patients diagnosed with confirmed VTE who received intravenous (IV) UFH therapy dosages and had their platelet counts monitored using defined parameters such as a nomogram or protocol. |
High |
Yes |
Yes |
APR-DRG/SOI or MS-DRG |
VTE-5 - Discharge Instructions |
This measure assesses the number of patients diagnosed with confirmed VTE that are discharged to home, home care, court/law enforcement or home on hospice care on warfarin with written discharge instructions that address all four criteria: compliance issues, dietary advice, follow-up monitoring, and information about the potential for adverse drug reactions/interactions. |
High |
No |
No |
N/A |
VTE-6 - Potentially-Preventable VTE |
This measure assesses the number of patients diagnosed with confirmed VTE during hospitalization (not present at admission) who did not receive VTE prophylaxis between hospital admission and the day before the VTE diagnostic testing order date. |
Low |
Yes |
Yes |
APR-DRG/ROM or MS-DRG |