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. 2013 May 5;29(4):241–256. doi: 10.1002/dmrr.2389

Table 3.

Summary of evidence for population-based screening for diabetes in early pregnancy among indigenous women in Australia, Canada, New Zealand and the United States

Screening criterion (no. publications) Evidence statement Quality of evidence for each statement and study references (H, high; M, moderate; L, low; VL, very low) Country
1. Prevalence (n = 49) Higher risk of undiagnosed T2DM in pregnancy and GDM H 86 Aus, Can, NZ, US, Int
M14,15,18,21,87115,123,127
L13,116122,220
VL126,145,169,221,222
Prevalence (trends) (n = 7) Prevalence of GDM and T2DM in pregnancy is increasing M21,125,167 Aus, Can, US, Int
L [223,224]
VL [225,226]
Natural history: risk for maternal development of DIP (n = 10) Maternal birth-weight low and high (u-shaped association) H 156 US
M [227]
Obesity M99,123 Can, US Aus
L 122
Genetic variants H [228] US
Thrifty genotype theory VL2,145,161 Can, Int
Thrifty phenotype theory VL 160 US
Natural history: risk to woman during pregnancy and birth (n = 12) Adverse birth outcomes (e.g. caesarean section and shoulder dystocia) H 140 Aus, Can, NZ, US
M9295,111,113,129,133
Increased risk of hospitalisation, associated with acute renal disease M 136 Can, US
L118,137
Natural history: maternal progression to T2DM (n = 8) Non-pregnant women with impaired glucose intolerance have higher risk of T2DM than pregnant women with impaired glucose tolerance H [229] US
L 13
Increased risk of progressing from GDM to T2DM M14,21,144 Can, US
L 13
VL 145
Faster progression from GDM to T2DM M96,112 Aus, Can
L 13
Progress from GDM to T2DM at a younger age M 96 Aus
Natural history: risk to infant in pregnancy and birth (n = 21) Increased risk of congenital abnormalities H 131 Aus, US
M15,108,132
VL 138
Increased risk of macrosomia H128,139,140 Aus, Can, NZ, US
M109,130,135,141143
L 128,230,231
Increased risk NICU admissions or poor birth outcomes M94,113,232 Aus, Can
L [233]
VL [234]
Natural history: long terms risks to infant (n = 31) Increased risk of obesity H146148 Can, US
L 128
VL 149
Increased risk of glucose intolerance H148,150152, M 153 US
Increased risk of GDM and T2DM H16,148,154157 Can, US, Int
M16,127,135,158,165,166,235
L128,163,164
VL2,159162
Increased risk renal disease H [236,237] US
2. Current screening practice and rates (n = 7) GDM screening practice and rates is variable M88,89,167,238 Aus, Can, NZ, US
L13,168
VL 169
Highest risk women (e.g. obese women) may be less likely to be screened M88,89 NZ, US
3. Preferences or values (n = 8) Suggest resources be culturally adapted, programs provide blood sugar data and emphasize opportunity to save money with health diet M 176 Can
Prefer greater community involvement (especially midwives and elders) and recognise importance of family ties and cultural values M 176 Can
VL171,177
Prefer group sessions and less direct advice (e.g. story-telling) VL 171 Can
Concern about weight gain in pregnancy but many barriers VL 178 Can
Many mixed understandings of risk and causes of DIP M 172 Aus, Can, US
L173,174
Diet (grandmothers), exercise and stress (mothers) cause DIP L 175 Can
4. Efficacy and cost (n = 3) Screening more sensitive than risk factor analysis alone H 180 US
One-step WHO method more sensitive than two-step NDDG method L 179 US
HBA1C tests not appropriate screening tool among indigenous women L 181 Int
5. Adequate treatment pathways (n = 6) Integrated community care may improve self-monitoring L 186 Aus
Standards for diagnosis and treatment VL 182 US
Early screening needed to reduce risk of GDM to mother and baby VL144,183,184 Aus, Can
Insulin pumps may improve glycaemic control L 185 NZ
6. Follow-up after pregnancy (n = 5) Low rates of follow-up screening for T2DM after pregnancy for women diagnosed with GDM M 14 Can, NZ, US
L 13
VL 188
Registers may improve follow-up VL 189 Can
High rates of glucose intolerance in women with DIP followed up after pregnancy L 188 NZ

DIP, diabetes in pregnancy; GDM, gestational diabetes mellitus; NDDG, National Diabetes Data Group; NICU, neonatal intensive care unit; T2DM, type 2 diabetes mellitus; WHO, World Health Organisation.