Table 3.
Rank | Research questions | Total score (confidence interval) | Agreement between scorers |
---|---|---|---|
55 |
Can stable surfactant with simpler novel modes of administration increase the use and availability of surfactant for preterm babies at risk of respiratory distress syndrome? |
71 (62–73) |
49 |
71 |
Can the method to diagnose fetal distress in labour be more accurate and affordable? |
66 (57–71) |
49 |
97 |
Can strategies for prevention and treatment of intrauterine growth restriction be developed? |
64 (51–68) |
46 |
105 |
Can novel tocolytic agents to delay or stop preterm labour be developed in order to reduce neonatal mortality and morbidity? |
63 (54–68) |
42 |
116 |
Can major causal pathways and risk factors for antepartum stillbirth be identified? |
61 (52–66) |
43 |
118 |
Can novel point of care diagnostics for congenital syphilis be identified in low resource setting to improve management? |
60 (53–64) |
49 |
120 |
Can novel antibiotic or other biological agents be identified? |
60 (51–65) |
40 |
121 |
Can the new method identify intrauterine growth restriction at the early stage (including biomarkers) and predict abnormal postnatal growth and body composition? |
60 (52–63) |
43 |
125 |
Can novel vaccines for maternal immunization be developed and evaluated to prevent newborn infections (eg, GBS, Klebsiella, E coli, Staph)? |
60 (51–64) |
41 |
129 | Can preterm birth be delayed or averted with antioxidant and/or nutrient supplementation (eg, Vitamin D, omega–3 fatty acids)? | 58 (48–63) | 42 |
GBS – group B streptococcus, Staph – staphylococcus