Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021;30(2):154-159.
doi: 10.1159/000511106. Epub 2020 Aug 25.

Prognostic Significance of Red Cell Distribution Width in Idiopathic Pulmonary Fibrosis and Combined Pulmonary Fibrosis Emphysema

Affiliations

Prognostic Significance of Red Cell Distribution Width in Idiopathic Pulmonary Fibrosis and Combined Pulmonary Fibrosis Emphysema

Aslıhan Gürün Kaya et al. Med Princ Pract. 2021.

Abstract

Objective: The red cell distribution width (RDW) is an inexpensive, readily available prognostic indicator of several diseases. RDW has been assessed as a prognostic biomarker in patients with idiopathic pulmonary fibrosis (IPF) in only one study; furthermore, the relationship between the RDW and combined pulmonary fibrosis emphysema (CPFE) has yet to be reported.

Subjects and methods: This single-center study was conducted between January 2015 and December 2018 in the Atatürk Chest Diseases and Chest Surgery Education and Research Hospital. Baseline characteristics, laboratory results, and survival status of patients were recorded.

Results: The RDW value was significantly higher in the CPFE group than in the IPF group (median [IQR 25-75]; 16.8 [15.5-19] vs. 15.3 [13.7-16.8], p = 0.028). High RDW values were correlated with carbon monoxide diffusion capacity (DLCO) (r: -0.653 p = 0.001), 6-minute walking test (6MWT) distance (r: -0.361 p = 0.017), arterial partial oxygen pressure (PaO2) (r: -0.692 p < 0.001), and systolic pulmonary arterial pressure (SPAP) (r: 0.349 p = 0.022) in patients with fibrotic lung disease. The RDW value was significantly higher in the exitus group than in the survivors (median [IQR 25-75]; 18.4 [15.4-19] vs. 15.2 [13.5-17.2], p = 0.016). A univariate Cox regression analysis identified DLCO, SPAP, PaO2, and RDW as potential covariates of mortality. In a multivariate analysis, the DLCO (HR 1.21, 95% CI 1.11-1.47, p = 0.012) and RDW level (HR 1.65, 95% CI 1.09-2.47, p = 0.023) remained independent predictors of mortality.

Conclusion: High RDW values appear to be a simple prognostic factor in patients with IPF or CPFE.

Keywords: Combined pulmonary fibrosis emphysema; Idiopathic pulmonary fibrosis; Red cell distribution width.

PubMed Disclaimer

Conflict of interest statement

All of the authors declare no conflict of interest.

Figures

Fig. 1
Fig. 1
Study flowchart diagram. IPF, idiopathic pulmonary fibrosis; CPFE, combined pulmonary fibrosis emphysema.
Fig. 2
Fig. 2
Comparison of RDW values between exitus and survivor patients. RDW, red cell distribution width.

References

    1. Simel DL, DeLong ER, Feussner JR, Weinberg JB, Crawford J. Erythrocyte anisocytosis. Visual inspection of blood films vs automated analysis of red blood cell distribution width. Arch Intern Med. 1988;148((4)):822–4. - PubMed
    1. Ichinose J, Murakawa T, Kawashima M, Nagayama K, Nitadori JI, Anraku M, et al. Prognostic significance of red cell distribution width in elderly patients undergoing resection for non-small cell lung cancer. J Thorac Dis. 2016;8((12)):3658–66. - PMC - PubMed
    1. Schepens T, De Dooy JJ, Verbrugghe W, Jorens PG. Red cell distribution width (RDW) as a biomarker for respiratory failure in a pediatric ICU. J Inflamm. 2017;14:12. - PMC - PubMed
    1. Zhou XY, Chen HL, Ni SS. Red cell distribution width in predicting 30-day mortality in patients with pulmonary embolism. J Crit Care. 2017;37:197–201. - PubMed
    1. Perlstein TS, Weuve J, Pfeffer MA, Beckman JA. Red blood cell distribution width and mortality risk in a community-based prospective cohort. Arch Intern Med. 2009;169((6)):588–94. - PMC - PubMed