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. 2023 Sep 1;13:07004. doi: 10.7189/jogh.13.07004

Table 5.

Top 20 research questions for Bangladesh (n = 54) with scores for each criterion, overall weighted RPS, and AEA

Rank Research questions Domain Answerability intermediate RPS Effectiveness intermediate RPS Deliverability intermediate RPS Burden intermediate RPS Equity intermediate RPS Weighted RPS AEA
1
How does the presence of skilled birth and neonatal care attendants influence survival outcomes for babies?
HPSR
0.956
0.965
0.948
0.752
0.947
0.911
0.860
2
What are the barriers and challenges of implementing facility-based KMC in LMICs?
HPSR
0.982
0.960
0.942
0.752
0.919
0.909
0.859
3
What is the prevalence and cause of neonatal sepsis in preterm, LBW and SGA infants in LMICs?
EPI
0.969
0.940
0.927
0.773
0.897
0.900
0.844
4
How can referral network and systems be strengthened for timely referral of women experiencing obstetric emergencies (including preterm labour) from rural/primary care to higher care level facilities in LMICs?
HPSR
0.944
0.954
0.935
0.718
0.965
0.900
0.840
5
How can acceptability and compliance KMC be increased in LMICs?
RIEI
0.924
0.956
0.952
0.750
0.864
0.888
0.827
6
How to promote early initiation and exclusive breast feeding of preterm, LBW and SGA infants in LMICs?
RIEI
0.941
0.954
0.943
0.708
0.904
0.887
0.821
7
Assess the effectiveness of community-based KMC in reducing neonatal mortality of clinically stable preterm and LBW infants?
HPSR
0.972
0.937
0.919
0.711
0.901
0.886
0.834
8
What are the clinical outcomes of preterm newborns discharged to continue KMC at home?
EPI
0.954
0.938
0.938
0.681
0.900
0.880
0.825
9
Assess the impact of quality improvement initiatives in improving KMC counselling.
HPSR
0.946
0.963
0.955
0.663
0.884
0.879
0.830
10
What are barriers and challenges to improving existing skin-to-skin practice in LMICs?
HPSR
0.955
0.944
0.934
0.712
0.857
0.879
0.844
11
How can transport and referral systems for preterm LBW, SGA newborns be improved or maximised in LMICs?
HPSR
0.939
0.914
0.923
0.722
0.909
0.879
0.837
12
What is the effect of antepartum complications in the current pregnancy (e.g. multiple gestation, cervical incompetence, preeclampsia, eclampsia, hypertension, diabetes etc.) on LBW, SGA and PTB in LMICs?
EPI
0.972
0.950
0.912
0.735
0.792
0.873
0.803
13
What is the effect of nutritional status (e.g. underweight, overweight and obesity, micronutrient deficiency etc.) on LBW, SGA and PTB in LMICs?
EPI
0.945
0.927
0.951
0.719
0.827
0.873
0.817
14
Evaluate interventions to screen women at risk of PTB during ANC (e.g. anaemia, preeclampsia, NCDs, malnutrition) and improve maternal and newborn outcomes in LMICs.
HPSR
0.941
0.916
0.914
0.700
0.903
0.872
0.805
15
What are barriers of doing ROP screening for all eligible preterm babies in LMICs?
HPSR
0.965
0.915
0.896
0.729
0.841
0.868
0.808
16
How can care for preterm and LBW newborns in remote community settings be improved?
HPSR
0.917
0.935
0.905
0.687
0.901
0.866
0.794
17
What are the short- and long-term health and developmental outcomes of babies born preterm, LBW, or SGA in LMICs?
EPI
0.951
0.926
0.933
0.673
0.847
0.864
0.787
18
How can clinical support and supervision of community health workers in the management of small and sick newborns be improved in LMICs?
HPSR
0.945
0.891
0.913
0.692
0.884
0.862
0.787
19
What are the barriers and enablers of improved accuracy of gestational age assessment in LMICs?
HPSR
0.946
0.936
0.886
0.685
0.851
0.860
0.803
20 Evaluate the effectiveness and cost-effectiveness of nutritional interventions in improving nutritional status of preterm infants in LMICs. EPI 0.937 0.893 0.892 0.692 0.899 0.860 0.807

LMICs – low and middle-income countries, KMC - Kangaroo Mother Care, RPS – research priority scores, AEA – average expert agreement, HPSR – health policy and systems research, EPI – epidemiological research, RIEI – research to improve existing interventions, RDNI – research to develop new interventions, LBW – low birth weight, SGA – small for gestational age, PTB – preterm birth, ROP – retinopathy of prematurity, NCD – non-communicable disease