AT&TSample data
AT&T · GLP-1 & Optimization

Clinical Pathway & Optimization

The GLP-1 patient journey from prescription through 12-month outcomes, with optimization levers and care team interventions.

Sample dataObserved

GLP-1 therapy pathway

30,000
Eligible
2,000
Enrolled
7%
1,766
Baseline complete
88%
1,678
Started therapy
95%
1,524
90-day active
91%
1,326
6-month persistent
87%
1,158
12-month outcomes
87%
1,009
Measurable improvement
87%

Funnel from 30,000 eligible to 1,009 with measurable improvement. Persistence rates: 90-day 1,524 → 6-month 1,326 → 12-month 1,158.

Clinical outcomes at current period

Measured
61%
Weight loss ≥5%
n = 1,285
45% benchmark
Measured
-9.9%
Avg weight change
from baseline
-5.2% benchmark
Measured
8 mmHg
Systolic BP drop
average reduction
4 mmHg benchmark
Measured
0.5%
HbA1c reduction
average reduction
0.3% benchmark

BMI change

Average BMI
33.8 → 30.5
among 643 members with paired measurements

Follow-up measurement coverage

Weight
638/83976%
Blood pressure
579/83969%
HbA1c
403/83948%
Lipids
445/83953%

Optimization levers

Dosage titration

82% at target dose

Of active members, 82% have reached the recommended maintenance dose. 18% are still titrating — monitored weekly by the care team.

Check-in cadence

2.8 actions/week

Active members average 2.8 meaningful actions per week (check-ins, messages, refills). Members below 1.5/week are flagged for outreach.

Discontinuation management

64 discontinued (7.6%)

Side effects (31%), cost/coverage (22%), and refill difficulties (16%) are the top reasons. Proactive outreach recovers ~30% of at-risk members.

Clinical monitoring

76% weight · 48% A1c

Follow-up measurement coverage varies by metric. Weight is well-captured; A1c and lipid gaps are addressed through lab partnerships.

Discontinuation analysis

64 members discontinued (3.8% of started). Top reasons and mitigation strategies:

Side effects
2031%
Cost / coverage
1422%
Refill difficulties
1016%
Clinical decision
813%
Other / unknown
1219%

All outcomes are measured from paired baseline and follow-up values. Benchmarks are illustrative, not validated external data. Clinical outcomes are shown only in properly aggregated, privacy-safe form.

Employee Privacy Protected by Design

Employer reporting is designed to present aggregate workforce and health-program insights without exposing individual clinical records. Small-group reporting restrictions help reduce the risk of employee identification.

Sample dataPrivacy-restricted reporting

Aggregated information is not described as HIPAA-de-identified unless applicable de-identification requirements have been satisfied and verified.

Sample Data — Demonstration Only. Fictional data, not actual patient records or validated outcomes.