048-18 Wyo. Code R. § 18-2

Current through April 27, 2019

Section 18-2 - Minimal Data Elements

Clinics/hospitals/physicians are required to collect and submit data for the defined clinical process related to the outcomes identified below. These data shall be submitted for each individual screened through the WCCEDP.

(a) Demographic Information:

(i) Patient age;

(ii) Gender; and

(iii) Family history of colon cancer.

(b) Clinical Outcomes:

(i) Screening outcome;

(ii) Screening results (normal, positive-biopsied);

(iii) Pathology results (polyp size, histology); and

(iv) Cancer characteristics (size, histology, stage and grade).
In addition, the WCCEDP will be responsible for outcome data relating to program process. The following outcomes will be reported to the Wyoming State Legislature with regard to program outcomes and successes:

(c) Process related outcomes:

(i) Outreach: number of individuals contacted by mail, telephone, social marketing campaigns, etc.;

(ii) Responses to outreach efforts;

(iii) Screening completion rates;

(iv) Number of patient's provided with transportation/translation services;

(v) Quality and timeliness of care; and

(vi) Patient satisfaction with screening program.

048-18 Wyo. Code R. § 18-2