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Figure 1.

Filovirus ward clinicians administering supportive treatment while concurrently recording clinical data during the Bundibugyo Uganda 2007–08 Ebola haemorrhagic fever outbreak.

Photo by Claude Mahoudeau.

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Table 1.

Self-reported demographics, days before seeking treatment at an Ebola ward, and contact histories of 26 patients with laboratory-confirmed Ebola haemorrhagic fever, Bundibugyo District, Uganda (November 2007–February 2008).

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Table 2.

Self-reported symptoms (15 patients), clinically observed symptoms (21 patients), and combined symptoms (26 patients) among hospitalised laboratory-confirmed EHF patients with known clinical outcome for whom data were recorded, Bundibugyo District, Uganda (November 2007–February 2008).

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Figure 2.

Frequency of non-haemorrhagic symptoms from self-reported day of symptom onset to clinical outcome, as absolute numbers and percentages, among symptomatic (9 deceased and 12 surviving) laboratory-confirmed Ebola haemorrhagic fever patients, Bundibugyo District, Uganda, November 2007–February 2008.

Note changes in denominator between self-reported and clinically observed sections.

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Figure 3.

Median duration in days of symptoms from self-reported onset until clinical outcome among 26 symptomatic laboratory-confirmed Ebola haemorrhagic fever patients, Bundibugyo District, Uganda (November 2007–February 2008).

Blue and red bars indicate general and haemorrhagic symptoms, respectively. *Day 0 = presentation to the Ebola ward. Whiskers indicate maximum duration of the self-reported symptoms prior to presentation to the Ebola ward for patient observations >1. Whiskers indicate maximum duration of the clinician-assessed symptoms at presentation to and during hospitalisation on the Ebola ward for patient observations >1. #Denominator contains female patients only (n = 9).

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Figure 4.

Frequency of haemorrhagic symptoms from self-reported day of symptom onset to clinical outcome, as absolute numbers and percentages, among symptomatic (9 deceased and 12 surviving) laboratory-confirmed Ebola haemorrhagic fever patients, Bundibugyo District, Uganda, November 2007–February 2008.

Note changes in denominator between self-reported and clinically observed sections.

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Figure 4 Expand

Table 3.

Treatment recorded for 19 hospitalised laboratory-confirmed Ebola haemorrhagic fever patients, by clinical outcome.

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Table 3 Expand