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Volume 3 Supplement 1


  • Poster presentation
  • Open Access

Icu and long-term mortality analisis of hematology patients admitted in icu. a 7 years review from a single spanish center

  • 1,
  • 2,
  • 1,
  • 1,
  • 2 and
  • 1
Intensive Care Medicine Experimental20153 (Suppl 1) :A244

  • Published:


  • Intensive Care Unit
  • Overall Survival
  • Multiple Myeloma
  • Chronic Lymphocytic Leukaemia
  • Haematological Malignancy


Improved survival in patients with haematological malignancy (HM) admitted to the intensive care unit (ICU) has largely been reported in uncontrolled cohorts. Newly diagnosed patients should be admitted, since their prognosis is still to be defined. Nevertheless the admission of the remaining patients remains a matter of substantial controversy.


To analyse the survival of HM patients admitted to ICU over a 7-year period (from 2008 to 2014).


We conducted a detailed retrospective study of sequential adult ICU admissions with HM in a single centre, considering numerous variables with regard to their influence on ICU and mortality. Overall survival (OS) was defined as the time from ICU admission to death from any cause, and surviving patients were censored at last follow-up. OS were calculated using the Kaplan-Meier method estimates and the differences assessed by the log-rank test. All P-value less than 0.05 were considered significant.


Overall, 67 HM patients were included, 62% were male, with a median age of 59 years (IQR: 19-82). The median APACHE II was 22 (IQR: 12-49). The hematologic diagnosis was as follow: 25 lymphomas (37%), 9 Multiple Myelomas (13%), 6 chronic lymphocytic leukaemia (9%) and 28 acute leukaemia or myeloproliferative or myelodisplasic syndromes in acute phase (41%). Disease status at the moment of UCI admission was: 19 (28%) complete response (CR), 24 (36%) newly diagnosis disease and 24 (36%) active disease (of those, 18 patients were refractory to disease specific treatment and 6 patients were chemosensitive); 67% of patients were on active oncologic treatment. Principal ICU diagnosis was sepsis (68%). Median number of organ failure were 2 (IQR: 0-4), and up to 36% of patients presented neutropenia at the moment of UCI admission. Median ICU length of stay was 7 days (IQR: 1-48) and hospital of stay 38 days (IQR: 8-109). ICU mortality was 46% (25% of patients died the first day of ICU admission, and 75% died within the first week).

The rates for ICU, 1-month, 6-month and 12 month mortality were 48%, 55% and 66%, respectively. With a median follow up of 18.5 months (IQR: 8-66), OS was 31%. Figure 1; Hematologic diagnosis (P = 0.04) Figure 2; status of the disease at the moment of ICU admission (P = 0.01) Figure 3; and the number of organ failure (≤ 2: 67% vs ≥ 3: 28%, P = 0.009) were the most powerful predictor variables associated with an increased mortality.
Figure 1
Figure 1

Overall Survival.

Figure 2
Figure 2

OS and type of HM in ICU admission.

Figure 3
Figure 3

OS and type of response in ICU admission.


OS of our HM patients is not worse than that recently reported from specialist units.The decision for or against ICU admission of patients with HM should become dependent of the underlying malignant disease and especially with the status of the disease at the moment of admission. Almost 50% of survivors are still alive one year after ICU admission, suggesting that an important subgroup of HM patients benefit from ICU admission.

Authors’ Affiliations

Intensive Care, Hospital 12 de Octubre, Madrid, Spain
Hematology, Hospital 12 de Octubre, Madrid, Spain


© Garcia Gigorro et al.; 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.