Readmission and mortality one year after acute hospitalization in older patients with explained and unexplained anemia - a prospective observational cohort study
© The Author(s). 2016
Received: 8 February 2016
Accepted: 16 May 2016
Published: 24 May 2016
Few studies have examined whether specific subtypes of anemia in older persons are more related to adverse outcomes such as hospital readmissions and death after acute hospitalization and post-acute care.
An observational prospective cohort study was conducted between 2011 and 2014. A total of 884 community-dwelling patients, ≥70 years of age were transferred from acute medical and orthopaedic hospital departments to a skilled nursing home where they were examined by comprehensive geriatric assessment and had laboratory tests taken for the investigation of anemia. They were divided into three major groups and compared; 1) no anemia (reference group), 2) explained anemia (renal insufficiency, iron deficiency, vitaminB12/folate deficiency or multifactorial anemia) and 3) unexplained anemia. The groups were compared, and association of anemia with hospital readmission and death was estimated by logistic regression analyses.
Compared to the patients with unexplained anemia (n=135), patients with explained anemia (n=275) had more often died (22 % vs. 14 %, p=0.05) and had more frequenlty been readmitted to hospital (39 % vs. 27 %, p=0.03). Compared to the patients without anemia (n=474), the patients with explained anemia had increased odds of hospital readmissions (OR = 1.54 (95 % CI: 1.05–2.25), p=0.03), while patients with unexplained anemia, (n=135), had neither increased odds of hospital readmissions, (OR=0.83, 95 % CI: 0.51–1.34, p=0.44) nor death (OR = 0.74, 95 % CI: 0.41–1.31, p=0.30), in adjusted regression analysis.
Since no increased risk of hospital readmissions or death was seen in older patients with unexplained anemia in the first year after acute hospitalization, no further invasive investigations might be necessary to investigate the cause of anemia in these patients. A close clinical follow up might be the best way to care for older patients with a mild and unexplained anemia.
KeywordsUnexplained anemia Readmission Mortality Elderly Hospitalization
The prevalence of anemia in older persons increases with age, and multifactorial causes related to age-associated renal insufficiency, microscopic bleeding, chronic inflammation, hormonal insufficiency and qualitative bone marrow alterations, like an age-associated diminished hematopoietic stem cell proliferative capacity or myelodysplastic syndrome, play important roles in the pathogenesis [1–3]. Anemia has been associated with several unfavorable outcomes, such as death [4, 5], the worsening of cardiovascular disease , cognitive impairment , falls  and functional dependence .
Most studies have focused on the risk of anemia in general, and have not examined whether specific subtypes of anemia are more related to unfavorable outcomes. In approximately one third of older persons no specific cause for the anemia, such as renal insufficiency, nutritional deficiency (iron, vitamin B12, folate) or a combination of these could be found, and the anemia is called unexplained anemia [10–12]. Two studies of community dwelling older people with unexplained anemia have described that people with unexplained anemia did not have any increased risk of mortality as compared to older people without anemia [13, 14]. However, to our knowledge, no study has investigated both the increased risk of hospital readmission and death in hospitalized home-dwelling elderly people with explained and unexplained anemia.
A different clinical outcome in patients with explained and unexplained anemia may imply different threshold for further investigation into the causes of anemia , as well as different follow-up and treatment.
Comparison of baseline characteristics and clinical outcome 12 months after acute hospitalization
Receive home care
Admitted after a fall
Other acute trauma
Other medical/pulmonary diseases
More than 5 diagnosis
Use > 5 drugs
Hb men, g/dL
Hb women, g/dL
Severe anemi (<10.6g/L)a
471 (319 -772)
Transferrin receptor, ml/L
NT pro-BnP, pmol/L
1 year follow up
>2 hospital admissions
The morning after arrival to the nursing home, they had a venous blood sample drawn. If the results of the blood test indicated that the patients had signs of iron deficiency anemia, and they had no occult blood loss suggestive of gastrointestinal malignancy, they were prescribed iron tablets. If the patients had folate or vitamin B12 deficiency, they were prescribed folate or vitamin B12 substitution. At discharge, all patients with anemia were asked to follow up with their general practitioner.
The data on patient’s demographic and baseline clinical characteristics were obtained from hospital records. During the first week in the nursing home comprehensive geriatric assessment was performed on >90 % of the patients using the Barthel index sumscore (BI) , the Norwegian version of the Mini Mental Status Examination, MMSE [17, 18], Geriatric Depression Scale GDS , and Mini Nutritional Assessment- Short Form; MNA-SF .
Data regarding hospital readmissions were obtained from electronic patient registers and digital health records at Haukeland and Haraldsplass hospitals (data obtained from 80 % of the patients). Mortality information (whether the patients were alive or dead 12 months after hospital discharge), was collected from the patient administrative system in the municipality (data obtained from 98 % of the patients).
Blood was collected into EDTA Vacutainer Tubes (Becton Dickinson) and hematological parameters (Hemoglobin level (Hb), MCV (mean corpuscular volume), white blood cells (WBS) and platelets,) were analyzed with an automated hematology analyzer (ADVIA 120, Bayer Diagnostics, Tarrytown, NY, USA).
Serum was obtained by collecting blood into Vacutainer Tubes with no additive (Becton Dickinson). Serum levels of creatinine (CV 1.8 %), C-reactive protein (CRP) (CV 3.3 %) and soluble transferrin receptor (TfR) (CV 3.5 %) were analyzed with Modular P, levels of cobalamin (vitamin B12) (CV 4.4 %), folate (CV 7.5 %) and NT-proBNP (N-Terminal pro brain-type natriuretic peptide) (CV 4.8 %) with Modular E and serum ferritin (CV 4.5 %) by Modular PP (F. Hoffman-La Roche Ltd, Basel, Switzerland).
The Modification of Diet in Renal Disease (MDRD) Study equation; GFR (glomerular filtration rate) (mL/min/1.73 m2) = 175 × (Scr)-1.154 × (Age)-0.203 × (0.742 if female), was used for estimating GFR. The equation does not require weight or height variables because the results are reported normalized to 1.73 m2 body surface area, which is an accepted average adult surface area. The equation has been validated in Caucasian populations between the ages of 18 and 70 with impaired kidney function (eGFR < 60 mL/min/1.73 m2) and has shown good performance for patients with all common causes of kidney disease .
Iron deficiency was assessed by measuring Ferritin and TfR, since other studies have demonstrated that these measurements give a more sensitive measure of iron-deficiency than the more commonly used Transferrin saturation (Serum-iron/Total Iron Binding Capacity (TIBC)) [22, 23]. Transferrin receptor rise, independent of inflammation, when the iron level available for erythropoiesis decrease .
N-Terminal pro brain-type natriuretic hormone (pro-BnP) (level > 225 pg/L ) has been demonstrated to be a sensitive marker clinical cardiovascular disease  and renal dysfunction , and was included as a measure of these comorbidities.
Definitions and subdivision of anemia subtypes
Anemia was classified according to the World Health Organization (WHO) definition as a haemoglobin concentration of less than 12 g/dL in women and less than 13 g/dL in men.
Severe anemi was defined as having a haemoglobin concentration in the lowest gender-specific tertile of the anemia patients. The 33.3 percentile of haemoglobin concentration both for men and women with anemia was 10.6 g/dL, and this value was used as cut-off for defining patients with severe anemia.
Renal anemia was defined as anemia combined with eGFR < 60 ml/min/1.73 m2 and normal levels of ferritin, folate and cobalamin
Iron deficiency anemia was defined as anemia combined with ferritin < 35 μg/L or TfR > 4.5 mg/L
Vitamin B12 or folate anemia was defined as anemia with vit B12 < 200 pmol/L or folate < 8 nmol/L, and normal levels for creatinine and ferritin and TfR
Multifactorial anemia was defined as anemia with more than one of the above explainable causes of the anemia.
Explainable anemia were defined as either renal anemia, iron deficiency anemia, vit B12/folate deficiency anemia or multiple cause anemia
Unexplainable anemia was defined as anemia without any known cause listed for the explained anemias.
Continuous data with a normal distribution was presented as mean (standard deviation) and compared with two sample t-test. Continuous data with a non-normal distribution was presented as median (interquartile range) and compared with the Mann–Whitney U test. Categorical data was presented as numbers (percentages) and compared with the chi-square test.
For identifying the clinical characteristics that were independently associated with hospital readmissions and death, odds ratios (ORs) with 95 % confidence intervals (CIs) were estimated using logistic regression models. The characteristics associated with p < 0.25 in univariate analysis were noted as likely predictors and included in multivariate, adjusted logistic regression models. When analysing hospital readmission as the outcome, the covariates age, >5 diagnoses, Barthel index, and the influence of five different admission diagnoses groups were included in the multivariate analysis. When analyzing mortality as outcome, the additional covariates male sex, hemoglobin concentration, renal failure and MMSE score were also included in multivariate analysis.
All analyses were performed using the Statistical Package for Social Science (IBM SPSS), version 20 for Windows.
Baseline patient characteristics and difference between patients with and without anemia
As shown in Table 1, the patients in general had rather good physical, cognitive and nutritional status, but still wide inter-individual variations were present in geriatric assessment tests.
Anemia based on the WHO criterias was present in 410 (46 %) of the patients while severe anemia was present in 130 (15 %) of the patients.
Compared to the patients without anemia, the anemic patients were older, more often male sex, more of them had suffered a hip fracture, they had worse ADL function (lower BI), they had more diagnoses and were using more medications. Their CRP and pro-BnP levels were higher, and more of them had renal insufficiency.
Unadjusted and adjusted Odds Ratios for hospital readmission and death 12 months after acute hospitalization
95 % CI
95 % CI
95 % CI
95 % CI
Difference in baseline characteristics and outcome in patients with subgroups of explainable anemia
As indicated in Fig. 1, one or more explainable cause (s) could be found for 275 (67 %) of all the patients with anemia. Renal insufficiency was the most common cause, and was present in 208 (76 %) of the patients with explained anemia (139 pure renal anemias + 69 multifactorial anemias), more often in men than in women.
Baseline characteristics and outcome 12 months after acute hospitalization in patients with different anemia subtypes
Explained anemia subtypes, n=275
119 (25 %)
52 (37 %)**
19 (35 %)
8 (67 %)**
35 (51 %)**
15 (3 %)
10 (7 %)
5 (9 %)
3 (25 %)
3 (4 %)
other orthopaedic trauma
144 (30 %)
39 (28 %)
20 (36 %)
2 (17 %)
10 (15 %)
116 (25 %)
37 (27 %)
12 (22 %)
2 (17 %)
20 (29 %)
68 (14 %)
24 (18 %)
8 (16 %)
3 (20 %)
15 (22 %)
other medical diseases
131 (28 %)
29 (21 %)
10 (19 %)
3 (20 %)
21 (30 %)
Vitamin B12, pmol/L
Transferrin receptor, ml/L
12 months follow up
> 2 hospital admissions
124 (26 %)
36 (39 %)
21 (50 %)**
2 (18 %)
23 (41 %)*
74 (16 %)
25 (21 %)
12 (23 %)
2 (18 %)
16 (23 %)
Difference in baseline characteristics and outcome in patients with unexplained and explained anemia
Characteristics and outcome 12 months after acute hospitalization in patients with explained and unexplained anemia
Unexplained vs explained anemia
119 (25 %)
51 (38 %)**
114 (42 %)**
Receive home care
196 (41 %)
43 (32 %)
114 (42 %)
Admitted after a fall
177 (38 %)
73 (55 %)**
103 (38 %)
15 (3 %)
30 (12 %)**
21 (8 %)*
Other acute trauma
144 (30 %)
51 (33 %)
63 (25 %)
116 (24 %)
36 (23 %)
66 (26 %)
68 (14 %)
16 (10 %)
49 (19 %)
131 (28 %)
21 (14 %)**
57 (22 %)
More than 5 diagnosis
266 (56 %)
76 (60 %)
186 (71 %)**
Use > 5 drugs
361 (77 %)
100 (75 %)
244 (90 %)**
Severe anemia (Hb < 10.6 g/L)a
38 (28 %)**
92 (36 %)**
Transferrin Receptor (TfR)
Pro-BnP > 225 pmol/L
90 (20 %)
21 (16 %)
110 (42 %)**
157 (34 %)
205 (75 %)**
91 (21 %)
110 (43 %)**
12 months follow up
>2 hospital admissions
114 (31 %)
29 (27 %)
86 (39 %)*
74 (16 %)
21 (14 %)
55 (22 %)*
Compared to the patients with explained anemia, the patients with unexplained anemias were more often women, were admitted after a fall and had suffered a hip fracture, but they had fewer diagnoses and were using less drugs. None of them (per definition) had iron deficiency nor renal insufficiency, and most of them did not have elevated NT-pro BnP, indicating no heart failure. The patients with unexplained anemia had no more hospitals admission or death than patients with no anemia. As shown in Table 2, no significant association was demonstrated between unexplained anemia and hospital admissions and unexplained anemia and death. When the analysis was repeated for patients with severe unexplained anemia, the results were not materially different.
As shown in Table 4, patients with explained anemia had more frequently been readmitted to hospital or had died during the first 12 months than patients without anemia. Furthermore, a significant association was demonstrated between explained anemia and hospital readmission in adjusted regression analysis, while no significant association between explained anemia and death was demonstrated in adjusted regression analysis (Table 2).
The main finding in the present study is that no increased risk of 1-year mortality and hospital readmissions could be demonstrated in older patients that had unexplained anemia, when they were discharged from acute hospitalization, compared to patients with no anemia. On the other hand, more patients with explained anemia died during the first year, and they had a higher risk of hospital readmissions, compared to patients without anemia. These findings imply that it is clinically important to distinguish between these two groups of anemias, because patients with unexplained and explained anemia may require different follow up and treatment.
To our knowledge no earlier studies have reported risk of hospital readmissions and death in older patients with explained and unexplained anemia, one year after acute hospitalization. However, our results are in agreement with the Leiden 85 plus study, which demonstrated no increased risk of mortality in 86 year old community dwelling persons with unexplained anemia compared to no anemia, after a 6-years follow-up . Similarly, the Women’s Health and Aging Study I, which included moderately to severely disabled women > 65 years of age, could not demonstrate increased mortality after five years in patients with unexplained anemia compared to non-anemic women .
Several other studies characterize a group of explained anemias related to chronic disease/chronic inflammation [10, 13, 26]. However, the definition for this anemia subtype is not uniform [11, 27]. Since a majority of our patients had chronic diseases, all of them had suffered an acute trauma or illness, and 80 % of them had an elevated CRP > 5, we decided, in line with the Leiden study , not to conduct any subgrouping of anemia patients with acute/chronic inflammation or chronic disease, but rather subdivide patients with explained and unexplained anemias based on simple, standardized laboratory measurements. The fractions of patients with unexplained and explained anemia in our study are in accordance with other studies of older patients living in the community [13, 14, 27], and with a small cohort of older patients from an acute medical hospital unit , and an university anemia clinic .
Our patients, with a mean age of 85 years, were living in the community, and 80 % of them returned home after a short stay in the hospital followed by post-acute care . Thus they may be partly comparable to both anemic persons living in the community [3, 13, 14, 29] and anemia patients from hospital cohorts [28, 30–32], but not strictly representative of a normal, home-dwelling elderly population. The overall prevalence of anemia in our study (47 %) was similar to other studies reporting anemia in a hospital setting [28, 32, 33], but lower than reported from long term care .
While no overall risk of mortality was demonstrated in the anemic population when applying the WHO definition, a significant association with mortality was demonstrated for the anemia patients with a hemoglobin concentration in the lower anemia tertile (10.6 g/dL). This is partly in agreement with a large study of 17 030 community dwelling older patients, reporting increased mortality in patients with a hemoglobin < 11gd/L , and with a previous study from long-term care demonstrating an association between high levels of hemoglobin and better survival . Unfortunately, no recording of the causes of death was recorded, thus we were unable to investigate whether different types of anemi were related to different causes of death.
Like other studies on anemia, renal insufficiency and iron deficiency were the most common causes of the explainable anemias, often together [14, 27]. In our study patients with iron deficiency anemia had the lowest Hb and the most frequent hospital readmissions, compared with the other anemia subgroups. Thus, the recognition of patients with iron deficiency anemia is particularly important to diagnose, as these patients may be more prone to hospital readmissions, and this type of anemia may be susceptible to treatment.
Clinical baseline differences were demonstrated between patients with unexplained and explained anemias. While both patient groups had rather mild anemia and elevated CRP, the patients with unexplained anemias more often had suffered a fall, even though they had fewer diagnoses, were using fewer drugs and had a lower pro-BnP, indicative of less cardiovascular disease. This suggests that the unexplained anemia in these patients might be more associated with frailty and the pro-inflammatory state of ageing, whereas the explained anemia is more related to multimorbidity. Although the reason for the observed differences in hospital readmission and mortality between patients with explained and unexplained anemia is not obvious from our study, we may speculate that the influence of both renal dysfunction, and possible heart failure, in combination with anemia, may influence the increased readmssion and mortality seen in the patients with explained anemia.
The findings in the present study may have clinical importance for the follow up and treatment of older patients diagnosed with anemia. When anemia is found in the elderly, it is important to determine if it is explained by age related physiological degeneration of bone marrow function or if there is an underlying disease of which the treatment can improve the anemia. We recommend that all patients with a subnormal hemoglobin level should have a repeated simple biochemical standard blood test including the measurements of Hb, MCV, eGFR, Ferritin, s-TfR (or se-Fe and TIBC), CRP, B12 and folate, to indicate whether the patients have an explained or unexplained anemia. If the patients have an explained anemia, further care should be directed towards handling these explained causes. For patients with iron deficiency, further search for GI disease or cancer should be sought before iron administration. If the patients have a renal anemia, particular care should be directed towards the use of nephrotoxic drugs and drug dosages, and treatment with Erythropoietin might be considered if blood serum levels are not elevated. For older patients with unexplained anemia, we support the conclusion from the Leiden study, that no further invasive investigations might be necessary in determining the cause of the anemia . However, we recommend that these patients are followed clinically, and that a screening test for frailty is included, as the anemia may precede, predispose or accelerate the development of frailty [34–36].
A limitation of the present study is that the follow up time of 12 months might be too short to assess the mortality risk in anemia patients. Furthermore, no formal assessment of multi-morbidity or frailty was done. The strength of our study is the prospective follow-up setting and the inclusion of a complete baseline geriatric evaluation, laboratory investigations and a one year follow-up. This enables new knowledge of both the clinical patient characteristics and the future clinical unfavourable outcomes, in older patients with unexplained and explained anemia.
In contrast to patients with an explained anemia, older anemic patients ≥ 70 years of age, without the presence of renal insufficiency, iron deficiency and B12/folate deficiency, had no increased risk of hospital readmission and death the first year after an acute hospitalization, compared to patients without anemia. This suggests that no further invasive investigations might be necessary to investigate the cause of the anemia, and that a close clinical follow up might be the best way to care for these older patients with a mild and unexplained anemia.
BI, Barthel index sumscore; CI, confidence interval; CRP, C-reactive protein; GDS, Geriatric Depression Scale; GFR, glomerular filtration rate; Hb, hemoglobin level; MCV, mean corposcular volume; MMSE, Mini Mental Status Examination; MNA-SF, mini nutritional assessment-short form; NT-pro BNP, N-Terminal pro brain-type natriuretic peptide; OR, odds ratio; TfR, transferrin receptor; WBS, white blood cells.
We thank Håkon Ersland and Arne Johannesen for their cooperation and work in providing data from the hospital’s electronic patient registers and digital health records, and Alex Sisto for assistance in the final preparation of the manuscript.
This study was funded by Western Norway Regional Health Authority (Grant number 911926). The funding source had no role in the study design, in the collection, analysis and interpretation of data, in the writing of the report or in the decision to submit the article for publication.
Availability of data material
The data will not be shared since sharing of dataset with other researchers was not included in the application and approval to the Regional Committee for Medical and Health Research.
JFA is the initiator, project leader and the first author of the manuscript. ALBM is responsible for the biochemical analysis and has contributed in the analyses of data and in the manuscript preparation. FL has contributed in the analyses of the data and in the manuscript preparation. CH is responsible for managing the patient database, retrieving the follow up information and has contributed in the manuscript preparation. RMN has been supervising the statistical work and has contributed to the manuscript preparation. AHR has been supervising the ongoing research, taken part in the initiation of the study and contributed to the manuscript preparation. All authors contributed to the study concept and design and critical review of the manuscript. All authors read and approved the final manuscript and agree to be accountable for all aspect of the work.
The authors declare that they have no competing interests.
Compliance with ethical standards
The study was approved by the Norwegian Regional Comittee for Medical and Health Research Ethics (2011/REKvest), and informed consent was signes by the patients before entering the study. No experimental interventions were performed.
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