the impact of haemoglobin on survival of haemodialysis patients

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P170
THE IMPACT OF HAEMOGLOBIN ON SURVIVAL OF HAEMODIALYSIS
PATIENTS
McCrink, L.M. [1], Marshall, A.H. [1], Cairns, K.J. [1], Fogarty, D. [2]
[1]
Centre of Statistical Science & Operational Research, Queen’s University Belfast
[2]
Belfast Health and Social Care Trust, Belfast
INTRODUCTION: With an ageing population, the analysis of chronic diseases is of increasing
importance and predicting outcomes and treatment strategies is important for patients and
limited resources. This research investigates the impact of haemoglobin (Hb) on haemodialysis
(HD) patients’ survival whilst accounting for informative censoring due to dropout. The impact
of various erythropoietin (EPO) drugs and a range of haematinic measurements, in particular
Mean Corpuscular Volume (MCV) and Mean Corpuscular Haemoglobin Concentration
(MCHC), on Hb levels are explored in this work.
METHODS: To simultaneously analyse the factors that affect a HD patient’s Hb levels and the
impact of this on their survival, a joint modelling approach to analyse longitudinal and survival
data was utilised. A linear mixed effects model linked with a Cox PH model was used to
represent the relationship between the repeated measurements of individuals and their survival
respectively. In doing so, informative censoring due to dropout is taken into account to provide
more precise results and thus interpretations. The data analysed in this research was obtained
from the NI renal information service and contains 1,340 HD patients with a total of 27,113
observations (average 20 observations per patient) collected over a ten year period (2002-2011).
RESULTS: This research highlights the large and significant impact between a patient’s MCV
and MCHC levels and their Hb levels. An increase of 10fL in MCV levels is shown to
increase Hb by 0.31g/dL whilst a 4g/dL increase in MCHC can cause Hb levels to increase by
over 1g/dL. Aranesp is shown to be associated with significantly higher Hb levels on average
than Epoetin Alfa (greater Hb by 0.23g/dL) or Epoetin Beta (greater Hb by 0.19g/dL). Patients
with higher Hb levels three months after commencing HD tend to have better survival
decreasing the hazard of death by 28% (Hazard Ratio=0.72). Greater decreases in Hb levels per
year are shown to be detrimental to survival, with a 1g/dL decrease on average each year
resulting in an increase in the hazard of death by 44% (Hazard Ratio=0.69). This research
illustrates the benefits of joint models that enable individual-specific survival curves to be
plotted, commencing at a patient’s last known measurement and changing dynamically over
time with new patient information.
CONCLUSION: This research presents evidence to encourage future research into anaemia in
HD patients to investigate the impact of particular EPO drugs and a patient’s MCV and MCHC
levels where patients with higher initial Hb levels and less change in Hb over time were shown
to have better survival. Through such longitudinal techniques, individualised survival curves
can be plotted that enable clinicians to predict the survival probabilities of patients as
individuals instead of through analysis of population trends.
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