Table 3.

OR for 6-week mortality by transport delays among paediatric and adult participants in the severe febrile illness social biopsy study, Tanzania, 2015–2016

Transport delay	Paediatric (n=160)*					Adult (n=156)†
	Cases (n=18)‡	Controls (n=142)‡	OR (95% CI)	P value	AF§ (95% CI)	Cases (n=34)‡	Controls (n=122)‡	OR (95% CI)	P value	AF§ (95% CI)
Patient reported a delay due to transport or cost of transport at any point	3 (16.7)	9 (6.3)	2.67 (0.66 to 10.76)	0.167	–	2 (5.9)	7 (5.7)	1.01 (0.18 to 5.52)	0.995	–
Patient delayed >1 hour to reach a facility at any point¶	7 (38.9)	26 (18.4)	3.27 (1.11 to 9.66)	0.032	27.0 (12.9 to 38.8)	13 (38.2)	20 (16.4)	3.03 (1.32 to 6.99)	0.009	25.6 (14.3 to 35.5)
Transport time to first facility (hours)	0.9 (2.0)**	0.5 (0.8)**	1.28 (0.89 to 1.85)	0.180	–	0.7 (0.9)	0.5 (1.0)	1.20 (0.86 to 1.67)	0.286	–
Transport time to last facility (hours)	1.3 (2.4)**	0.8 (1.2)**	1.23 (0.94 to 1.60)	0.126	–	0.8 (1.2)**	0.8 (1.6)**	1.06 (0.84 to 1.34)	0.600	–
Total number of dichotomous transport delays present	0.6 (0.7)**	0.2 (0.5)**	2.45 (1.12 to 5.33)	0.024	–	0.4 (0.6)**	0.2 (0.5)**	2.16 (1.07 to 4.36)	0.031	–

*Paediatric analysis is based on 9:1 nearest-neighbour matching with deduplication based on age and gender.

†Adult analysis is based on 6:1 nearest-neighbour matching with deduplication based on age and gender.

‡Data are reported as n (%) unless otherwise noted.

§Attributable fraction is reported as a percentage and is only given for the dichotomous delays significantly associated with mortality on conditional logistic regression analysis.

¶We also estimated the OR for this delay at the first facility, the last facility and the first or last facility, none of which were significant.

**Data reported as mean (SD).

AF, attributable fraction.