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. 2019 Mar 8;6(1):e000280. doi: 10.1136/bmjresp-2018-000280

Table 1.

Demographics and outcomes

Patients (n) n=survived bCPAP (%)* n=bCPAP death (%)* OR of death (95% CI)
Total 117 79 (68%) 38 (32%)
Demographics
 Male† 58 40 (69%) 18 (31%) 1.00
 Female† 51 34 (67%) 17 (33%) 1.11 (0.50 to 2.49)
 Median (IQR) age in months 7 (2– 15) 6 (2–15) 7 (4–14)
Age (months)†
 <1 6 3 (50%) 3 (50%) 1.00
 1–12 76 53 (70%) 23 (30%) 0.43 (0.81 to 2.31)
 13–24 23 17 (74%) 6 (26%) 0.35 (0.06 to 2.25)
 25–48 10 5 (50%) 5 (50%) 1.00 (0.13 to 7.57)
Organ failure
 VSPNA 62 54 (87%) 8 (13%)
 VSPNA no comorbidities‡; including children<1 month 59 51 (86%) 8 (14%) 1.00
 VSPNA with comorbidities‡ 3 3 (100%) 0 (0%)
 VSPNA no comorbidities; no HIV exposure/infection, no malaria, no suspected TB‡ 14 14 (100%) 0 (0%)
 VSPNA; no comorbidities; no HIV exposure/infection, no malaria; including suspected TB 19 19 (100%) 0 (0%)
 MOF >1 organ dysfunction‡: respiratory dysfunction and at least one further organ dysfunction 55 25 (45%) 30 (55%) vs VSPNA: 8.10 (3.25 to 20.18)¶
 MOF >2 organ dysfunctions‡: (respiratory dysfunction and at least two other organ dysfunctions) 21 9 (43%) 12 (57%)
Malnutrition†
 SAM 28 10 (36%) 18 (64%) 7.59 (2.88 to 19.97)§
 MAM 13 8 (62%) 5 (38%) 2.63 (0.75 to 9.29)
 No MAM or SAM 73 59 (81%) 14 (19%) 1.00
HIV status
 Infected or exposed 22 10 (45%) 12 (55%) 4.97 (1.53 to 16.13)¶
 Negative 36 29 (81%) 7 (19%) 1.00
 Unknown 59 40 (68%) 19 (32%) 1.97 (0.73 to 5.29)
bCPAP delivery device
 Cylinder 50 35 (70%) 15 (30%) 1.00
 Concentrator 48 30 (62%) 18 (38%) 1.40 (0.60 to 3.25)
 Unrecorded 17 12 (71%) 5 (29%) 0.97 (0.29 to 3.25)
Treatment initiation location
 High dependency unit 29 17 (59%) 12 (41%) 1.55 (0.65 to 3.70)
 Emergency zone 83 57 (69%) 26 (31%) 1.00
Intubation**
 No 100 77 (77%) 23 (23%) 1.00
 Yes 15 2 (13%) 13 (87%) 21.8 (4.6 to 103.5)††
 Median (IQR) treatment duration (hours) 24 (24–60) 24 (24–60) 24 (24–48)

Comorbidities: congenital heart diseases (4 (children with congenital heart diseases: AVSD: 2 (1 with trisomy 21), VSD: 1; PDA: 1 (and trisomy 21))), neurodisability (cerebral palsy (1), hydrocephalus (1), neuromuscular disorder (1), severe thorax wall infection/defect (1). bCPAP, bubble continuous positive airway pressure; HB, haemoglobin; MAM, moderate acutemalnutrition; MOF, multiorgan failure; SAM, severe acute malnutrition; TB, tuberculosis; VSPNA, very severe pneumonia. AVSD, Atrio-ventricular Septum Defect; VSD, Ventricular Septum Defect; PDA, Persistent Ductus Arteriosus

*The percentages given in column 3 and 4 describe the ratios to the subtotals documented in column 2.

†Information on sex (male/female) was not recorded for eight patients. Information on age was not recorded for two patients. Information on malnutrition (MAM or SAM) was not recorded for three patients.

‡Organ dysfunction: respiratory failure (signs of very severe pneumonia50, signs of shock or ‘impaired circulation’28, severe anaemia (HB< 7 g/dl), coma/prolonged convulsions, clinical signs of liver/renal failure.

§p<0.0001.

¶p=0.008.

**In 2 of the 117 patients the information on potential intubation and ventilation was not documented.

††p<0.000.

bCPAP, bubble continuous positive airway pressure; HB, haemoglobin; MAM, moderate acutemalnutrition; MOF, multiorgan failure; SAM, severe acute malnutrition; TB, tuberculosis; VSPNA, very severe pneumonia.