The choice between an SGLT2i or GLP1RA - SGLT2i is typically preferable if renal disease or heart failure predominates (GLP1RA is preferable if CVA predominates). If the HbA1c remains above target in this high-risk group, dual SGLT2i (and GLP1RA therapy is recommended but not funded in NZ).

Formal Recommendations

Recommendation & Evidence

Recommendation StrengthNone
Evidence LevelNone

Categories

Treatment initiation, intensification, and adjustmentSodium–glucose cotransporter 2 (SGLT2) inhibitorsGlucagon-like peptide 1 (GLP-1) receptor agonists and multi-receptor agonists
Recommendation No.: 2-2024-035E-030R Guideline No.: 2-2024-035EGuideline: Samoa MOH National Diabetes Guidelines

PICO Question

P

Population

People with type 2 diabetes at high cardiorenal risk requiring treatment escalation

I

Intervention

Prefer an SGLT2 inhibitor when kidney disease or heart failure predominates; prefer a GLP-1 receptor agonist when cerebrovascular disease predominates; use both if HbA1c remains above target

C

Comparison

SGLT2 inhibitor versus GLP-1 receptor agonist according to the predominant comorbidity

O

Outcome

Reduced kidney, heart failure, cerebrovascular, and glycemic risk

Evidence Information

Evidence No.-
Evidence-
Evidence LevelNone
Recommendation StrengthNone
Statement TypeFormal Recommendations

Guideline Information

Guideline NameSamoa MOH National Diabetes Guidelines
Guideline No.2-2024-035E
AuthorAlec Ekeroma
Guideline TypeGuideline
Year2024
OrganizationMinistry of Health Samoa
RegionOceania
CountrySamoa
Conflict of InterestNo
DOI
Target Population所有糖尿病患者(包括1型糖尿病、2型糖尿病、妊娠期糖尿病、儿童及青少年),特别是萨摩亚及太平洋人群,包括高危人群(超重/肥胖、有家族史、既往糖尿病史等)
Journal
Recommendation Strength Methodology
Evidence Level Methodology

Other Information

Living GuidelineNo
Rapid AdviceNo
UpdatedNo
Recommendation Count0
Reference Count50
Guideline TopicComprehensive
CategoriesTreatment initiation, intensification, and adjustment, Sodium–glucose cotransporter 2 (SGLT2) inhibitors, Glucagon-like peptide 1 (GLP-1) receptor agonists and multi-receptor agonists
Created At2026-07-28 17:47:18
Updated At2026-07-28 17:47:18