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Table 8 Association between Sponsor and clinical outcomes: Tolerance symptoms

From: Association between funding source, methodological quality and research outcomes in randomized controlled trials of synbiotics, probiotics and prebiotics added to infant formula: A Systematic Review

Tolerance

Source of funding

Positive*

Negative*

Neutral*

Chi-square p value

Fisher’s exact p value

n (%)$$

n (%)$$

n (%)$$

Colic N = 13

Industry

1 (7.7)

 

11 (84.6)

0.764

1.00

 

None/Not clear

     
 

Non industry

  

1 (7.7)

  

Spitting up/Regurgitation N = 26

Industry

2 (7.7)

1 (3.8)

17 (65.4)

0.907

1.00

 

None/Not clear

  

4 (15.4)

  
 

Non industry

  

2 (7.7)

  

Vomiting N = 31

Industry

1 (3.2)

 

23 (74.2)

0.860

1.00

 

None/Not clear

  

5 (16.1)

  
 

Non industry

  

2 (6.5)

  

Crying fussiness N =22

Industry

3 (13.6)

1 (4.5)

14 (63.6)

0.581

1.00

 

None/Not clear

  

4 (18.2)

  
 

Non industry

  

0

  

Gastric residuals, Abdominal distension N = 5

Industry

  

1 (20)

0.659

1.00

 

None/Not clear

  

1 (20)

  
 

Non industry

1 (6.7)

 

2 (40)

  

Volume of formula consumed/daily intake N = 31

Industry

3 (9.7)

1 (3.2)

18 (58.1)

0.758

1.00

 

None/Not clear

  

4 (12.9)

  
 

Non industry

  

5 (16.1)

  

Days to full enteral feeding N = 9

Industry

  

4 (44.4)

0.325

0.444

 

None/Not clear

1 (11.1)

 

1 (11.1)

  
 

Non industry

1 (11.1)

 

2 (22.2)

  
  1. $$Overall percentage.
  2. *Positive: synbiotic, probiotic or prebiotic supplementation had a statistically significant effect, p < 0.05. There were significant differences between study groups (in favour of experimental group).
  3. *Neutral: synbiotic, probiotic or prebiotic supplementation did not have a statistically significant effect, p > 0.05, No significant differences between study groups.
  4. *Negative: synbiotic, probiotic or prebiotic supplementation had a statistically significant increase in an adverse event / negative outcome, p < 0.05.