Table 2.

Secondary outcomes

CharacteristicIV Ig, N = 21Oral antibiotics, N = 42
Number of clinically documented infections, n 39 56 
Number of participants with clinically documented infections, n (%)   
0 infections 3 (14) 18 (43) 
1 infection 5 (24) 12 (29) 
2 infections 8 (38) 2 (5) 
≥ 3 infections 5 (24) 5 (24) 
Number of microbiologically documented infections, n 11 16 
Number of participants with microbiologically documented infection, n (%)   
0 infections 13 (62) 34 (81) 
1 infection 6 (29) 2 (5) 
2 infections 1 (5) 5 (12) 
≥ 3 infections 1 (5) 1 (2) 
Participants with resistant organism identified, n   
Cotrimoxazole resistant 
Extended-spectrum β-lactamases 
Multidrug resistant 
Number of deaths, n (%) 2 (9.5) 1 (2.4) 
Number of infection deaths, n (%) 1 (4.8) 1 (2.4) 
IgG (g/L), median (IQR) 9.1 (7.4-11.1) 4.2 (3.3-5.6) 
Number of treatment-related AEs , n   
Grade 1 
Grade 2 11 
Grade 3 
Duration of IV antibiotics (d), median (IQR) 2.0 (2.0-2.0) 3.0 (2.5-3.5) 
Hospital duration (d), median (IQR) 2.0 (1.0-4.5) 2.0 (1.0-4.0) 
CharacteristicIV Ig, N = 21Oral antibiotics, N = 42
Number of clinically documented infections, n 39 56 
Number of participants with clinically documented infections, n (%)   
0 infections 3 (14) 18 (43) 
1 infection 5 (24) 12 (29) 
2 infections 8 (38) 2 (5) 
≥ 3 infections 5 (24) 5 (24) 
Number of microbiologically documented infections, n 11 16 
Number of participants with microbiologically documented infection, n (%)   
0 infections 13 (62) 34 (81) 
1 infection 6 (29) 2 (5) 
2 infections 1 (5) 5 (12) 
≥ 3 infections 1 (5) 1 (2) 
Participants with resistant organism identified, n   
Cotrimoxazole resistant 
Extended-spectrum β-lactamases 
Multidrug resistant 
Number of deaths, n (%) 2 (9.5) 1 (2.4) 
Number of infection deaths, n (%) 1 (4.8) 1 (2.4) 
IgG (g/L), median (IQR) 9.1 (7.4-11.1) 4.2 (3.3-5.6) 
Number of treatment-related AEs , n   
Grade 1 
Grade 2 11 
Grade 3 
Duration of IV antibiotics (d), median (IQR) 2.0 (2.0-2.0) 3.0 (2.5-3.5) 
Hospital duration (d), median (IQR) 2.0 (1.0-4.5) 2.0 (1.0-4.0) 

AEs, adverse events.

No treatment-related grade 4 or 5 AEs reported.

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