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The mortality effect was confirmed in 2008 with a hospital mortality of 7% and a 6 month mortality of 10% (Table 2).
The cumulative 12 month mortality of survivors of ICU treatment in the UK varies between 35% and 43% [ 4, 5].
Similarly, a reduction in 24 hour urine output of just 500 ml is associated with a HR for 6 month mortality of 1.09 (95% CI, 1.04 to 1.14; P <0.001), which translates into a 9% increase in risk of death.
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The 6-month mortality of patients who received NIV was lower than in our study (27%).
In this cohort, the 6-month mortality of 17% was mainly due to cardiovascular causes.
A 2006 study from a Scottish transplant centre demonstrated 12-month mortality of 81% in ICU admissions with decompensated alcoholic cirrhosis [4]; other non-UK transplant centres have reported 6-month mortality of between 62 and 71% [15 17].
Twenty-one (43 %) patients were transplanted without ECMO with a 3-month mortality of 14%% (Group 1).
Long-term outcome data from cirrhotic patients admitted to general ICUs are also scarce, with one European centre reporting 6-month mortality of 60% amongst all admissions, another reporting 12-month mortality of 82% and one UK centre reporting 12-month mortality of 59% [3, 18, 19].
Among them, 16 patients presented no contraindications for HELT and were transplanted with a 3-month mortality of 0%% (Group 2).
Isolated IJVT has been shown to have a 12-month mortality of 42% though death was related more to underlying illness than to IJVT or PE [3].
In a cohort of 233 patients with similar age and disease severity, Boumendil et al. showed a 2-month mortality of 41%[38]].
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