eCQM Title | Cesarean Birth |
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eCQM Identifier (Measure Authoring Tool) | 334 | eCQM Version Number | 5.2.000 |
NQF Number | 0471e | GUID | fc52d0de-b53d-4ccf-816e-1e527748d2d9 |
Measurement Period | January 1, 20XX through December 31, 20XX | ||
Measure Steward | The Joint Commission | ||
Measure Developer | The Joint Commission | ||
Endorsed By | National Quality Forum | ||
Description |
Nulliparous women with a term, singleton baby in a vertex position delivered by cesarean birth |
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Copyright |
Measure specifications are in the Public Domain. LOINC(R) copyright 2004-2022 Regenstrief Institute, Inc. This material contains SNOMED Clinical Terms(R) (SNOMED CT[R]) copyright 2004-2022 International Health Terminology Standards Development Organisation. ICD-10 copyright 2022 World Health Organization. All Rights Reserved. |
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Disclaimer |
These performance measures are not clinical guidelines and do not establish a standard of medical care and have not been tested for all potential applications. The measures and specifications are provided without warranty. |
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Measure Scoring | Proportion | ||
Measure Type | Outcome | ||
Stratification |
None |
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Risk Adjustment |
None |
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Rate Aggregation |
None |
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Rationale |
The removal of any pressure to not perform a cesarean birth has led to a skyrocketing of hospital, state and national cesarean birth (CB) rates. Some hospitals’ CB rates were over 50%. Hospitals with CB rates at 15-20% have infant outcomes that are just as good and better maternal outcomes (Symum et al., 2021). There is no data that higher rates improve any outcomes, yet the CB rates continue to rise. This measure seeks to focus attention on the most variable portion of the CB epidemic, the term labor CB in nulliparous women. This population segment accounts for the large majority of the variable portion of the CB rate and is the area most affected by subjectivity. As compared to other CB measures, what is different about Nulliparous, Term, Singleton, Vertex (NTSV) CB rate is that there are clear cut quality improvement activities that can be done to address the differences. Main et al., 2012 found that over 60% of the variation among hospitals can be attributed to first birth labor induction rates and first birth early labor admission rates. The results showed if labor was forced when the cervix was not ready the outcomes were poorer. Rosenstein et al., 2021 also showed that labor and delivery guidelines can make a difference in labor outcomes. Many authors have shown that physician factors, rather than patient characteristics or obstetric diagnoses are the major driver for the difference in rates within a hospital (Berkowitz et al.,1989; Goyert et al., 1989; Luthy et al., 2003; Symum et al., 2021). The dramatic variation in cesarean rates seen in all populations studied is striking. (Cesarean rates varied tenfold in US hospitals nationwide across hospitals, from 7.1% to 69.9% and there was a 15-fold variation among low-risk women, from 2.4% to 36.5% (Kozhimannil et al., 2013). A reduction in the number of NTSV patients delivering by cesarean birth will result in increased patient safety, a substantial decrease in maternal and neonatal morbidity and substantial savings in health care costs. Successful quality improvement efforts incorporate audit and feedback strategies combined with provider and nurse education, guidelines and peer review. The measure will assist health care organizations to track NTSV patients delivering by cesarean birth to reduce the occurrence. Nulliparous women have 4-6 times the cesarean birth rate than multiparous women thus the NTSV population is the largest driver of primary cesarean birth rate (Sakala et al., 2020). NTSV has a large variation among facilities, thus identifying an important population on which to focus quality improvement efforts. In addition, a reduction in primary cesarean births will reduce the number of women having repeat cesarean births (almost 90% of mothers who have a primary cesarean birth will have subsequent cesarean birth (CDC, 2020)). Thus, improvement in the rates of cesarean birth for the first birth will reduce the morbidity of all future births and avoid all the controversies with trial of labor after cesarean/elective repeat cesareans. |
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Clinical Recommendation Statement |
The American College of Obstetrics and Gynecology (ACOG) report, Evaluation of Cesarean Delivery, recognizes the importance of the Nulliparous, Term Singleton Vertex (NTSV) population as the optimal focus for measurement and quality improvement action. A reduction in the number of nulliparous patients with live term singleton newborns in vertex position delivering by cesarean birth will result in increased patient safety, a substantial decrease in maternal and neonatal morbidity and substantial savings in health care costs. |
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Improvement Notation |
Within Optimal Range. The Joint Commission does not want to encourage inappropriately low Cesarean rates that may be unsafe to patients. Acceptable PC-02 rates are 30% or lower, however there is not an established threshold for what rate may be too low. PC-06 serves as a balancing measure for PC-02 to guard against any unanticipated or unintended consequences and to identify unforeseen complications that might arise as a result of quality improvement activities and efforts for this measure. In order to identify areas for improvement, hospitals may want to review results based on specific ICD-10 codes or patient populations. Data could then be analyzed further determine specific patterns or trends to help reduce cesarean births. |
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Reference |
Reference Type: CITATION Reference Text: 'Agency for Healthcare Research and Quality. (2002). AHRQ Quality Indicators Guide to Inpatient Quality Indicators: Quality of Care in Hospitals Volume, Mortality, and Utilization. Revision 4 (December 22, 2004). AHRQ Pub. No. 02-RO204.' |
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Reference |
Reference Type: CITATION Reference Text: 'American College of Obstetricians and Gynecologists. (2000). Task Force on Cesarean Delivery Rates. Evaluation of Cesarean Delivery. (Developed under the direction of the Task Force on Cesarean Delivery Rates, Roger K. Freeman, MD, Chair, Arnold W. Cohen, MD, Richard Depp III, MD, Fredric D. Frigoletto Jr, MD, Gary D.V. Hankins, MD, Ellice Lieberman, MD, DrPH, M. Kathryn Menard, MD, David A. Nagey, MD, Carol W. Saffold, MD, Lisa Sams, RNC, MSN and ACOG Staff: Stanley Zinberg, MD, MS, Debra A. Hawks, MPH, and Elizabeth Steele)' |
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Reference |
Reference Type: CITATION Reference Text: 'Bailit, J.L., Garrett, J.M., Miller, W.C., McMahon, M.J., & Cefalo, R.C. (2002). Hospital primary cesarean delivery rates and the risk of poor neonatal outcomes. Am J Obstet Gynecol. 187(3):721-7.' |
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Reference |
Reference Type: CITATION Reference Text: 'Bailit, J. & Garrett, J. (2003). Comparison of risk-adjustment methodologies. Am J Obstet Gynecol.102:45-51.' |
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Reference |
Reference Type: CITATION Reference Text: 'Bailit, J.L., Love, T.E., & Dawson, N.V. (2006). Quality of obstetric care and risk-adjusted primary cesarean delivery rates. Am J Obstet Gynecol.194:402.' |
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Reference |
Reference Type: CITATION Reference Text: 'Bailit, J.L. (2007). Measuring the quality of inpatient obstetrical care. Ob Gyn Sur. 62:207-213.' |
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Reference |
Reference Type: CITATION Reference Text: 'Berkowitz, G.S., Fiarman, G.S., Mojica, M.A., et al. (1989). Effect of physician characteristics on the cesarean birth rate. Am J Obstet Gynecol. 161:146-9.' |
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Reference |
Reference Type: CITATION Reference Text: 'Center for Disease Control (2020) Recent trends in vaginal birth after cesarean delivery: United States, 2016-2018. Retrieved from National Center for Health Statistics: https://www.cdc.gov/nchs/products/databriefs/db359.htm' |
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Reference |
Reference Type: CITATION Reference Text: 'Cleary, R., Beard, R.W., Chapple, J., Coles, J., Griffin, M., & Joffe, M. (1996). The standard primipara as a basis for inter-unit comparisons of maternity care. Br J Obstet Gynecol. 103:223-9.' |
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Reference |
Reference Type: CITATION Reference Text: 'DiGiuseppe, D.L., Aron, D.C., Payne, S.M., Snow, R.J., Dieker, L., & Rosenthal, G.E. (2001). Risk adjusting cesarean delivery rates: a comparison of hospital profiles based on medical record and birth certificate data. Health Serv Res.36:959-77.' |
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Reference |
Reference Type: CITATION Reference Text: 'Goyert, G.L., Bottoms, F.S., Treadwell, M.C., et al. (1989). The physician factor in cesarean birth rates. N Engl J Med.320:706-9.' |
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Reference |
Reference Type: CITATION Reference Text: 'Kozhimannil, K. B., Law, M. R., & Virnig, B. A. (2013). Cesarean delivery rates vary tenfold among US hospitals; reducing variation may address quality and cost issues. Health affairs (Project Hope), 32(3), 527–535. https://doi.org/10.1377/hlthaff.2012.1030' |
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Reference |
Reference Type: CITATION Reference Text: 'Le Ray, C., Carayol, M., Zeitlin, J., Berat, G., & Goffinet, F. (2006). Level of perinatal care of the maternity unit and rate of cesarean in low-risk nulliparas. Am J Obstet Gynecol. 107:1269-77.' |
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Reference |
Reference Type: CITATION Reference Text: 'Luthy, D.A., Malmgren, J.A., Zingheim, R.W., & Leininger, C.J. (2003). Physician contribution to a cesarean delivery risk model. Am J Obstet Gynecol.188:1579-85.' |
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Reference |
Reference Type: CITATION Reference Text: 'Main E.K., Bloomfield, L., & Hunt, G. (2004). Development of a large-scale obstetric quality-improvement program that focused on the nulliparous patient at term. Am J Obstet Gynecol.190:1747-58.' |
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Reference |
Reference Type: CITATION Reference Text: 'Main, E. K., Chang, S. C., Cape, V., Sakowski, C., Smith, H., & Vasher, J. (2019). Safety Assessment of a Large-Scale Improvement Collaborative to Reduce Nulliparous Cesarean Delivery Rates. Obstetrics and gynecology, 133(4), 613–623. https://doi.org/10.1097/AOG.0000000000003109' |
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Reference |
Reference Type: CITATION Reference Text: 'Main, E.K., Moore, D., Farrell, B., Schimmel, L.D., Altman, R.J., Abrahams, C., et al., (2006). Is there a useful cesarean birth measure? Assessment of the nulliparous term singleton vertex cesarean birth rate as a tool for obstetric quality improvement. Am J Obstet Gynecol. 194:1644-51.' |
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Reference |
Reference Type: CITATION Reference Text: 'Main, E. K., Morton, C. H., Melsop, K., Hopkins, D., Giuliani, G., & Gould, J. B. (2012). Creating a public agenda for maternity safety and quality in cesarean delivery. Obstetrics and gynecology, 120(5), 1194–1198. https://doi.org/10.1097/aog.0b013e31826fc13d' |
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Reference |
Reference Type: CITATION Reference Text: 'Romano, P.S., Yasmeen, S., Schembri, M.E., Keyzer, J.M., & Gilbert, W.M. (2005). Coding of perineal lacerations and other complications of obstetric care in hospital discharge data. Am J Obstet Gynecol.106:717-25.' |
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Reference |
Reference Type: CITATION Reference Text: 'Rosenstein, M. G., Chang, S. C., Sakowski, C., Markow, C., Teleki, S., Lang, L., Logan, J., Cape, V., & Main, E. K. (2021). Hospital Quality Improvement Interventions, Statewide Policy Initiatives, and Rates of Cesarean Delivery for Nulliparous, Term, Singleton, Vertex Births in California. JAMA, 325(16), 1631–1639. https://doi.org/10.1001/jama.2021.3816' |
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Reference |
Reference Type: CITATION Reference Text: 'Sakala, C., Belanoff, C., & Declercq, E. R. (2020). Factors Associated with Unplanned Primary Cesarean Birth: Secondary Analysis of the Listening to Mothers in California Survey. BMC pregnancy and childbirth, 20(1), 462. https://doi.org/10.1186/s12884-020-03095-4' |
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Reference |
Reference Type: CITATION Reference Text: 'Symum, H., & Zayas-Castro, J. L. (2021). A Multistate Decomposition Analysis of Cesarean Rate Variations, Associated Health Outcomes, and Financial Implications in the United States. American journal of perinatology, 10.1055/s-0041-1736538. Advance online publication. https://doi.org/10.1055/s-0041-1736538' |
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Reference |
Reference Type: CITATION Reference Text: 'U.S. Department of Health and Human Services. (n.d.). Reduce cesarean births among low-risk women with no prior births-MICH-06. Retrieved from Healthy People 2030: https://health.gov/healthypeople/objectives-and-data/browse-objectives/pregnancy-and-childbirth/reduce-cesarean-births-among-low-risk-women-no-prior-births-mich-06' |
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Reference |
Reference Type: CITATION Reference Text: 'Yasmeen, S., Romano, P.S., Schembri, M.E., Keyzer, J.M., & Gilbert, W.M. (2006). Accuracy of obstetric diagnoses and procedures in hospital discharge data. Am J Obstet Gynecol. 194:992-1001.' |
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Definition |
Parity: The number of pregnancies reaching 20 weeks gestation regardless of the number of fetuses or outcomes Gravidity: The number of pregnancies, current and past, regardless of the pregnancy outcome Preterm Birth: The number of births >= 20 weeks and < 37 weeks gestation, regardless of outcome Term Birth: The number of births >= 37 weeks gestation, regardless of outcome Nulliparous: Parity = 0 or Gravidity = 1 or Preterm & Term Births both = 0 |
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Guidance |
Vertex position is modeled implicitly, as the measure excludes deliveries with abnormal presentations. Patients who do not receive prenatal care and have no documented gestational age or estimated due date are implicitly excluded from the measure, as gestational age is required to meet denominator criteria. This measure allows for 3 approaches to determine gestational age (GA) in the following order of precedence: 1. The GA is calculated using the American College of Obstetricians and Gynecologists ReVITALize guidelines.* 2. The GA is obtained from a discrete field in the electronic health record. This option is only used when the calculated GA is not available. 3. The GA is based on ICD10 or SNOMED codes indicative of weeks gestation. This option is only used when results from items #1 and #2 (see above) are not available. Wherever gestational age is mentioned, relative to the delivery, the intent is to capture the last estimated gestational age prior to or at the time of delivery. *ACOG ReVITALize Guidelines for Calculating Gestational Age: Gestational Age = (280-(EDD minus Reference Date))/7 --Estimated Due Date (EDD): The best obstetrical Estimated Due Date is determined by last menstrual period if confirmed by early ultrasound or no ultrasound performed, or early ultrasound if no known last menstrual period or the ultrasound is not consistent with last menstrual period, or known date of fertilization (e.g., assisted reproductive technology) --Reference Date is the date on which you are trying to determine gestational age. For purposes of this eCQM, Reference Date would be the Date of Delivery. Note however the calculation may yield a non-whole number and gestational age should be rounded off to the nearest completed week. For example, 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. The timing relationship of relevantDatetime 42 weeks or less before TimeOfDelivery is applied to the data elements of parity, gravida, preterm/term live births for which prenatal records may include relevant information. Note: The eCQM and chart-based measure slightly digress in the denominator and denominator exclusion logic. The chart-based measure excludes single stillbirth and patients with multiple gestations from the denominator. These concepts are mutually exclusive of the denominator requirement of live singleton newborn and therefore the logic does not address single stillbirth nor multiple gestation. Parity, preterm and term live births may be updated by the electronic health record software or by clinicians during a delivery encounter. To capture the pre-delivery value, organizations may need to create a rule or calculation to capture the number prior to the delivery start time. "Gravida", "PretermBirth", "TermBirth" and "Parity" results should be submitted via QRDA I as integer and not as number or quantity. This eCQM is an episode-based measure. An episode is defined as each inpatient hospitalization or encounter that ends during the measurement period. This version of the eCQM uses QDM version 5.6. Please refer to the eCQI resource center (https://ecqi.healthit.gov/qdm) for more information on the QDM. |
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Transmission Format |
TBD |
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Initial Population |
Inpatient hospitalizations for patients age >= 8 years and < 65 admitted to the hospital for inpatient acute care who undergo a delivery procedure with a discharge date that ends during the measurement period |
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Denominator |
Inpatient hospitalizations for nulliparous patients who delivered a live term singleton newborn >= 37 weeks' gestation See Guidance and Definition Sections for more details. |
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Denominator Exclusions |
Inpatient hospitalizations for patients with abnormal presentation, placenta previa, placenta accreta or vasa previa during the encounter |
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Numerator |
Inpatient hospitalizations for patients who deliver by cesarean section |
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Numerator Exclusions |
None |
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Denominator Exceptions |
None |
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Supplemental Data Elements |
For every patient evaluated by this measure also identify payer, race, ethnicity, sex and calculated gestational age. |
PCMaternal."Delivery Encounter with Age Range"
"Singleton Delivery Encounters at 37 Plus Weeks Gravida 1 Parity 0, No Previous Births"
"Delivery Encounter with Abnormal Presentation, Placenta Previa, Placenta Accreta or Vasa Previa"
"Delivery Encounter with Cesarean Birth"
None
None
None
"Encounter with Abnormal Presentation" union "Encounter with Placenta Previa, Placenta Accreta or Vasa Previa"
PCMaternal."Delivery Encounter with Age Range" DeliveryEncounter where PCMaternal."CalculatedGestationalAge" ( DeliveryEncounter ) >= 37
"Singleton Delivery Encounters at 37 Plus Weeks Gravida 1 Parity 0, No Previous Births" QualifyingEncounter with ["Procedure, Performed": "Cesarean Birth"] CSection such that Global."NormalizeInterval" ( CSection.relevantDatetime, CSection.relevantPeriod ) during PCMaternal."HospitalizationWithEDOBTriageObservation" ( QualifyingEncounter )
PCMaternal."Delivery Encounter with Age Range" DeliveryEncounter where PCMaternal."CalculatedGestationalAge" ( DeliveryEncounter ) is null and PCMaternal."LastEstimatedGestationalAge" ( DeliveryEncounter ) >= 37 weeks
"Delivery Encounter with Calculated Gestational Age Greater than or Equal to 37 Weeks" union "Delivery Encounter with Estimated Gestational Age Greater than or Equal to 37 Weeks" union "Delivery Encounter with Gestational Age Greater than or Equal to 37 Weeks Based on Coding"
PCMaternal."Delivery Encounter with Age Range" DeliveryEncounter let CGA: PCMaternal."CalculatedGestationalAge" ( DeliveryEncounter ), EGA: PCMaternal."LastEstimatedGestationalAge" ( DeliveryEncounter ) where CGA is null and EGA is null and exists ( DeliveryEncounter.diagnoses EncounterDiagnoses where EncounterDiagnoses.code in "37 to 42 Plus Weeks Gestation" )
"Singleton Delivery Encounters at 37 Plus Weeks Gravida 1 Parity 0, No Previous Births"
"Delivery Encounter with Abnormal Presentation, Placenta Previa, Placenta Accreta or Vasa Previa"
"Singleton Delivery Encounters at 37 Plus Weeks Gravida 1 Parity 0, No Previous Births" QualifyingEncounter let LastAbnormalPresentation: Last(["Assessment, Performed": "Abnormal Presentation"] AbnormalPresentation where Global."EarliestOf"(AbnormalPresentation.relevantDatetime, AbnormalPresentation.relevantPeriod)before or on PCMaternal."LastTimeOfDelivery"(QualifyingEncounter) sort by Global."EarliestOf"(relevantDatetime, relevantPeriod) ) where exists ( QualifyingEncounter.diagnoses EncounterDiagnosis where EncounterDiagnosis.code in "Abnormal Presentation" ) or Global."EarliestOf" ( LastAbnormalPresentation.relevantDatetime, LastAbnormalPresentation.relevantPeriod ) during QualifyingEncounter.relevantPeriod
"Singleton Delivery Encounters at 37 Plus Weeks Gravida 1 Parity 0, No Previous Births" QualifyingEncounter where exists QualifyingEncounter.diagnoses EncounterDiagnosis where EncounterDiagnosis.code in "Placenta Previa or Accreta or Vasa Previa"
PCMaternal."Delivery Encounter with Age Range" DeliveryEncounter where exists ( DeliveryEncounter.diagnoses EncounterDiagnoses where EncounterDiagnoses.code in "Delivery of Singleton" )
PCMaternal."Delivery Encounter with Age Range"
"Delivery Encounter with Cesarean Birth"
"Encounter with Age Range" EncounterWithAge with ["Procedure, Performed": "Delivery Procedures"] DeliveryProcedure such that Global."NormalizeInterval" ( DeliveryProcedure.relevantDatetime, DeliveryProcedure.relevantPeriod ) starts during day of "HospitalizationWithEDOBTriageObservation"(EncounterWithAge)
["Encounter, Performed": "Encounter Inpatient"] EncounterInpatient where AgeInYearsAt(date from start of EncounterInpatient.relevantPeriod)>= 8 and AgeInYearsAt(date from start of EncounterInpatient.relevantPeriod)< 65 and EncounterInpatient.relevantPeriod ends during day of "Measurement Period"
//This definition establishes a variable of CGA (Calculated Gestational Age). CGA is a supplemental data element to store the calculated gestational age result from the "CalculatedGestationalAge" function. The data element enables the capturing and saving of the CGA for data analysis post data receipt. Hospitals do not need to submit any additional data to comply with this definition. "Delivery Encounter with Age Range" QualifyingEncounter let CGA: "CalculatedGestationalAge"(QualifyingEncounter) return { QualifyingEncounter, CGA }
["Patient Characteristic Ethnicity": "Ethnicity"]
["Patient Characteristic Payer": "Payer"]
["Patient Characteristic Race": "Race"]
["Patient Characteristic Sex": "ONC Administrative Sex"]
( "Delivery Encounter with Gestational Age Greater than or Equal to 37 Weeks" intersect "Encounter with Singleton Delivery" ) SingletonEncounterGE37Weeks where ( ( "LastGravida"(SingletonEncounterGE37Weeks)= 1 ) or ( "LastParity"(SingletonEncounterGE37Weeks)= 0 ) or ( ( "LastHistoryPretermBirth"(SingletonEncounterGE37Weeks)= 0 ) and ( "LastHistoryTermBirth"(SingletonEncounterGE37Weeks)= 0 ) ) )
PCMaternal."Variable Calculated Gestational Age"
Last(["Assessment, Performed": "[#] Pregnancies"] Gravida where Global."EarliestOf"(Gravida.relevantDatetime, Gravida.relevantPeriod)42 weeks or less before PCMaternal."LastTimeOfDelivery"(Encounter) and Gravida.result is not null sort by Global."EarliestOf"(relevantDatetime, relevantPeriod) ).result as Integer
Last(["Assessment, Performed": "[#] Births.preterm"] PretermBirth where Global."EarliestOf"(PretermBirth.relevantDatetime, PretermBirth.relevantPeriod)42 weeks or less before PCMaternal."LastTimeOfDelivery"(Encounter) and PretermBirth.result is not null sort by Global."EarliestOf"(relevantDatetime, relevantPeriod) ).result as Integer
Last(["Assessment, Performed": "[#] Births.term"] TermBirth where Global."EarliestOf"(TermBirth.relevantDatetime, TermBirth.relevantPeriod)42 weeks or less before PCMaternal."LastTimeOfDelivery"(Encounter) and TermBirth.result is not null sort by Global."EarliestOf"(relevantDatetime, relevantPeriod) ).result as Integer
Last(["Assessment, Performed": "[#] Parity"] Parity where Global."EarliestOf"(Parity.relevantDatetime, Parity.relevantPeriod)42 weeks or less before PCMaternal."LastTimeOfDelivery"(Encounter) and Parity.result is not null sort by Global."EarliestOf"(relevantDatetime, relevantPeriod) ).result as Integer
if ( HasStart(period)) then start of period else end of period
Earliest(NormalizeInterval(pointInTime, period))
not ( start of period is null or start of period = minimum DateTime )
if pointInTime is not null then Interval[pointInTime, pointInTime] else if period is not null then period else null as Interval<DateTime>
// Age = (280-(Estimated Delivery Date minus Reference Date/Delivery Date))/7 ( 280 - ( difference in days between "LastTimeOfDelivery"(Encounter)and "LastEstimatedDeliveryDate"(Encounter)) ) div 7
//HospitalizationWithEDOBTriageObservation returns the total interval from the start of any immediately prior emergency department visit or OB Triage visit through the observation visit to the discharge of the given encounter. Encounter Visit let ObsVisit: Last(["Encounter, Performed": "Observation Services"] LastObs where LastObs.relevantPeriod ends 1 hour or less on or before start of Visit.relevantPeriod sort by end of relevantPeriod ), VisitStart: Coalesce(start of ObsVisit.relevantPeriod, start of Visit.relevantPeriod), EDOBTriageVisit: Last(["Encounter, Performed": "ED Visit and OB Triage"] LastEDOBTriage where LastEDOBTriage.relevantPeriod ends 1 hour or less on or before VisitStart sort by end of relevantPeriod ) return Interval[Coalesce(start of EDOBTriageVisit.relevantPeriod, VisitStart), end of Visit.relevantPeriod]
//This function identifies the last time the Estimated Delivery Date was assessed 42 weeks or less prior to or on delivery and stores the result of that assessment. Last(["Assessment, Performed": "Delivery date Estimated"] EstimatedDateOfDelivery where Global."EarliestOf"(EstimatedDateOfDelivery.relevantDatetime, EstimatedDateOfDelivery.relevantPeriod)42 weeks or less before or on "LastTimeOfDelivery"(Encounter) and EstimatedDateOfDelivery.result is not null sort by Global."EarliestOf"(relevantDatetime, relevantPeriod) ).result as DateTime
Last(["Assessment, Performed": "Estimated Gestational Age at Delivery"] EstimatedGestationalAge where Global."EarliestOf"(EstimatedGestationalAge.relevantDatetime, EstimatedGestationalAge.relevantPeriod)24 hours or less before or on "LastTimeOfDelivery"(Encounter) and EstimatedGestationalAge.result is not null sort by Global."EarliestOf"(relevantDatetime, relevantPeriod) ).result as Quantity
Last(["Assessment, Performed": "Date and time of obstetric delivery"] TimeOfDelivery where Global."EarliestOf"(TimeOfDelivery.relevantDatetime, TimeOfDelivery.relevantPeriod)during "HospitalizationWithEDOBTriageObservation"(Encounter) and TimeOfDelivery.result as DateTime during "HospitalizationWithEDOBTriageObservation"(Encounter) sort by Global."EarliestOf"(relevantDatetime, relevantPeriod) ).result as DateTime
["Patient Characteristic Ethnicity": "Ethnicity"]
["Patient Characteristic Payer": "Payer"]
["Patient Characteristic Race": "Race"]
["Patient Characteristic Sex": "ONC Administrative Sex"]
PCMaternal."Variable Calculated Gestational Age"
Measure Set |
eMeasure Perinatal Care (ePC) |
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