Included studies of the aetiology of sepsis in young infants
Year(s) of study | Study location | Hospital type | Study type | Inclusion criteria | 0–30 day-old infants, positive/total tested | Older infants, positive/total tested | Community-acquired pathogens only | |
---|---|---|---|---|---|---|---|---|
Anah et al, 200835 | 2002–4 | Calabar, Nigeria | Tertiary hospital | Retrospective review of laboratory records | – | 363/717 (51%) | – | Unclear what proportion of infections were nosocomial |
Ayoola et al, 200322 | 1998 | Ibadan, Nigeria | Tertiary hospital | Prospective | Post-neonatal infants presenting with fever | – | 1–12 months old: 39/102 (38%) | Yes |
Al Zwaini, 200234 | 2000–1 | Ramadi, Iraq | Tertiary hospital | Prospective | Clinical features of sepsis and a positive blood culture | 118/? (a total of 1331 newborns admitted during study period) | – | Probably not all, included referred children |
Darmstadt et al, 200930 | 2004–6 | Bangladesh | Community surveillance | Prospective | Clinical features of sepsis | 30/500 (6%) | – | 40% likely early onset sepsis |
Kapoor et al, 200525 | 2000–1 | Delhi, India | Tertiary hospital | Prospective | Clinical features of sepsis | 125/632 (20%) | – | Probably not all, included referred children |
Karki and Parija, 199926 | 1999 | Dharan, Nepal | Tertiary hospital | Prospective | Clinical features of sepsis | 46/77 (60%) | – | Yes |
Kayange et al, 201027 | 2009 | Mwanza, Tanzania | Tertiary hospital | Prospective | Clinical features indicative of sepsis | 149/300 (50%) | – | Yes |
Meremikwu et al, 200523 | 1996–2002 | Calabar, Nigeria | Tertiary hospital | Retrospective review of laboratory records | Clinical features indicative of sepsis, or fever without a localised lesion | 271/533 (51%) | 1–12 months old: 113/252 (45%) | Likely |
Milledge et al, 200512 | 1996–2001 | Blantyre, Malawi | Tertiary hospital | Retrospective | Clinical features of sepsis | 784/? | – | Yes |
Mugalu et al, 200632 | 2002 | Mulago, Uganda | Tertiary hospital | Prospective | Clinical features of sepsis | 110/193 (57%) | – | Likely |
Ojukwu et al, 200633 | 2002–3 | Abakaliki, Nigeria | Tertiary hospital | Prospective | Clinical features of sepsis | 33/138 (24%) | – | Yes |
Quiambao et al, 200724 | 1994–2000 | Bohol Island, Philippines | First-level referral hospital | Prospective | Severe pneumonia, suspected sepsis or meningitis | 22/424 (5%) | 0–60 days old: 12/343(3%) | Yes |
Sharma et al, 200228 | 2001–2 | India | Tertiary hospital | Prospective | Fever or other clinical features of sepsis | 521/1534 (34%) | 1–12 months old: 194/1165 | Yes |
Shitaye et al, 201029 | 2006–7 | Addis Ababa, Ethiopia | Tertiary hospital | Prospective | Clinical features of sepsis | 135/302 (45%) | – | Mostly (98%) early onset sepsis |
Sigaúque, 200921 | 2001–6 | Manhica district, southern Mozambique | Rural hospital | Prospective | All admissions (bacteraemia) | 154/952 (16%) | 29 days–12 months old: 520/6892 (8%) | Yes |
Tsering et al, 201136 | 2007–8 | Sikkim, India | Tertiary hospital | Prospective | Clinical features of sepsis | 80/363(22%) | – | Not clear in all cases |
Viswanathan, 201113 | 2008–9 | Birbhum, India | Rural hospital | Prospective | Clinical features of sepsis | 77/? | – | Likely mostly community acquired. Of 77 positive cultures, 45 were inborn babies and 32 were out-born |
Waliullah et al, 200931 | 2005–6 | Bangladesh | Tertiary hospital | Prospective | Clinical features of sepsis | 30/80 (38%) | – | Unclear whether early or late onset |
WHO Young Infant Study, 199920 | 1993 | The Gambia, Ethiopia, Philippines, Papua New Guinea, Tanzania | Primary care facilities, secondary or tertiary hospitals | Prospective multicentre study | Clinical features of sepsis | 84/? | 0–90 days old: 167/4552 (4%) | Yes, only results for early onset sepsis used, as it is unclear what proportion of late onset sepsis was community acquired |