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An attempt at an epidemiological explanation - Epib.nl

An attempt at an epidemiological explanation - Epib.nl

An attempt at an epidemiological explanation - Epib.nl

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Chapter 5The striking difference in the risk of f<strong>at</strong>al disease for female versus male p<strong>at</strong>ients stiUst<strong>an</strong>ds after adjustment for the other covari<strong>at</strong>es (OR = 2.3; 95%-confidence interval(95%-CI): 1.2 - 4.7).Serious sequelae were reported in 44 of the 515 surviving p<strong>at</strong>ients (8.5%). In 4survivors the presence or absence of sequelae was not specified. Five p<strong>at</strong>ients had 2sequelae <strong>an</strong>d 4 p<strong>at</strong>ients more th<strong>an</strong> 2 sequelae. Scars after skin necrosis were reportedin 20 p<strong>at</strong>ients, <strong>an</strong>d amput<strong>at</strong>ion in 4. Hearing loss (16 p<strong>at</strong>ients), paralysis of a cr<strong>an</strong>ialnerve (5), hydrocephalus (3), cerebral <strong>at</strong>rophy (2) <strong>an</strong>d seizures (2) were the mostfrequent neurological sequelae. Other sequelae were mental retard<strong>at</strong>ion (3 p<strong>at</strong>ients),disturb<strong>an</strong>ce of vision, hemiparesis,peripheral neurop<strong>at</strong>hy, hypopituitarism <strong>an</strong>dbehavioural disturb<strong>an</strong>ce (each in 1 p<strong>at</strong>ient). The distribution of sequelae among thevarious serogroups is shown in Table 6. The absence of p<strong>at</strong>ients with sequelae indisease due to the uncommon serogroups is noticeable. There was no associ<strong>at</strong>ion ofthe occurrence of sequelae (either combined or separ<strong>at</strong>ed into neurological <strong>an</strong>dhemodynamic sequelae) with serogroup, serotype, sub type or immunotype of thecaus<strong>at</strong>ive agent, or with the gender or age of the p<strong>at</strong>ient. Sequelae occurred in 6.5%of the meningitic p<strong>at</strong>ients, in 9.0% of the septicemic p<strong>at</strong>ients, <strong>an</strong>d in 13.9% ofp<strong>at</strong>ients ,vith both meningitis <strong>an</strong>d septicemia (X' = 5.6; 2 df: P = .061). The sequelaer<strong>at</strong>e among p<strong>at</strong>ients with a predisposing factor (19.0%) was higher th<strong>an</strong> among tbosewithout (8.3%; Fisher's exact test: P = .100). In a mUltiple logistic regression model,o<strong>nl</strong>y the clinical present<strong>at</strong>ion was signific<strong>an</strong>tly associ<strong>at</strong>ed with the occurrence ofsequelae. The OR for the occurrence of sequelae for septicemic versus meningiticp<strong>at</strong>ients was 1.4 (95%-CI: .6 - 3.2), <strong>an</strong>d for p<strong>at</strong>ients with both septicemia <strong>an</strong>dmeningitis versus meningitic cases 2.3 (95 %-CI: 1.1 - 4.7) .Table 6. Sequelae among 515 p<strong>at</strong>ients with systemic mcningococc.11 disease in the Netherl<strong>an</strong>ds, 1989·1990 according to serogroup (percentage of p<strong>at</strong>ients with sequelae in indic<strong>at</strong>ed serogroupbetween brackets)No. of p<strong>at</strong>ients (percentage of sequelae)Sero- No. of Hearing Damage of other cr<strong>an</strong>ial Other neurologic."lI or Scars <strong>an</strong>d/or Total"group survivors loss nerve/mot. disturb<strong>an</strong>ce psychological disturb<strong>an</strong>ce amput<strong>at</strong>ionA 11 1 (9.1) 1 (9.1) 0 0 2(18.2)B 399 12 (3.0) 4 (1.0) 6 (1.5) 16 (4.0) 38 (9.5)C 90 3 (3.3) 1 (1.1) 0 4 (4.4) 8 (8.9)Other 15 0 0 0 0 0Total 515 16 (3.1) 6 (1.2) 6 (1.2) 20 (3.9) 48. some p<strong>at</strong>ients bad more th<strong>an</strong> 1 sequela70

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