dc.contributor.author
Doehner, Wolfram
dc.contributor.author
Scherbakov, Nadja
dc.contributor.author
Schellenberg, Tim
dc.contributor.author
Jankowska, Ewa A.
dc.contributor.author
Scheitz, Jan F.
dc.contributor.author
von Haehling, Stephan
dc.contributor.author
Joebges, Michael
dc.date.accessioned
2024-12-20T12:32:07Z
dc.date.available
2024-12-20T12:32:07Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/46060
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-45769
dc.description.abstract
Background: Iron deficiency (ID) is a common co-morbidity in patients with cardiovascular disease and contributes to impaired functional capacity. The relevance of ID in patients in recovery after acute stroke is not known. We assessed the prevalence of ID and anaemia in relation to functional capacity and to recovery during early rehabilitation after stroke.
Methods: This observational study enrolled consecutively 746 patients with ischaemic or haemorrhagic stroke at in-patient early rehabilitation (age 68 +/- 13 years, female 47%, ischaemic stroke 87%). Functional capacity was assessed before and after rehabilitation using Barthel index (reha-BI), motricity index (MI), trunk control test (TCT), and functional ambulatory category (FAC). ID was defined as ferritin <100 mu g/L or as transferrin saturation (TSAT) 5 mg/L. Anaemia was defined as Hb < 12 g/dL (women) and <13 g/dL (men).
Results: The prevalence of ID and anaemia before rehabilitation were 45% and 46%, respectively, and remained high at discharge (after 27 +/- 17 days) at 40% and 48%, respectively. Patients with ID had lower functional capacity compared with patients without ID (reha-BI 20 [+/- 86] vs. 40 [+/- 80], MI 64 [+/- 66] vs. 77 [+/- 41], TCT 61 [+/- 76] vs. 100 [+/- 39], FAC 1 [+/- 4] vs. 4 [+/- 4]; median [IQR], all P < 0.001). ID was related to inflammation (OR 2.68 [95% CI 1.98-3.63], P < 0.001), female sex (OR 2.13 [95% CI 1.59-2.85], P < 0.001), haemorrhagic stroke (OR 1.70 [95% CI 1.11-2.61], P = 0.015), initial treatment on stroke unit (OR 3.59 [95% CI 1.08-11.89], P < 0.001), and anaemia (OR 2.94 [95% CI 2.18-3.96], P < 0.001), while age, BMI, and renal function were not related to ID. In adjusted analysis, ID was associated with low functional capacity in all functional scores: reha-BI (OR 1.66 [95% CI 1.08-2.54], P = 0.02), motricity index (OR 1.94 [95% CI 1.36-2.76], P < 0.001), trunk control test (OR 2.34 [95% CI] 1.64-3.32, P < 0.001) and functional ambulatory category (OR 1.77 [95% CI 1.2-2.63], P < 0.02). Functional capacity improved during rehabilitation regardless of presence of ID, but functional outcome remained significantly lower in patients with ID at the end of rehabilitation (rehab BI and MI, both P < 0.001).
Conclusions: Iron deficiency and anaemia are common and persistent findings in patients after acute stroke. ID and anaemia are independently related to lower functional capacity after acute stroke and to poor functional outcome after rehabilitation. Regular assessment of iron status may identify patients at risk of low functional recovery.
en
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject
Ischaemic stroke
en
dc.subject
Haemorrhagic stroke
en
dc.subject
Iron deficiency
en
dc.subject
Rehabilitation
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Iron deficiency is related to low functional outcome in patients at early rehabilitation after acute stroke
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1002/jcsm.12927
dcterms.bibliographicCitation.journaltitle
Journal of Cachexia, Sarcopenia and Muscle
dcterms.bibliographicCitation.number
2
dcterms.bibliographicCitation.originalpublishername
Wiley
dcterms.bibliographicCitation.pagestart
1036
dcterms.bibliographicCitation.pageend
1044
dcterms.bibliographicCitation.volume
13
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
DEAL Wiley
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
35166066
dcterms.isPartOf.issn
2190-5991
dcterms.isPartOf.eissn
2190-6009