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. 2020 May 20;20:145. doi: 10.1186/s12890-020-1176-0

Correction to: Assessment of stigma in patients with cystic fibrosis

Smita Pakhale 1,2,3,4,, Michael Armstrong 1, Crystal Holly 1,2,3, Rojiemiahd Edjoc 1, Ena Gaudet 2, Shawn Aaron 1,2,3,4, Giorgio Tasca 1,2,3, William Cameron 1,2,3, Louise Balfour 2,3
PMCID: PMC7238593  PMID: 32434540

Correction to: BMC Pulm Med (2014) 14:76

https://doi.org/10.1186/1471-2466-14-76

Following publication of the original article [1], the authors reported an error in Table 2 of the article.

Namely, rows ‘2.’ and ‘9.’ are missing from the table.

Please now see (the correct version of) Table 2 provided in this correction.

Table 2.

The baseline CF Stigma Scale scores

N = 45 Strongly
Disagree = 1
N(%)
Disagree = 2
N(%)
Agree = 3
N(%)
Strongly
Agree = 4
N(%)
1. I am very careful who I tell that I have CF. 6 (13.3) 17 (37.8) 10 (22.2) 11 (24.4)
2. I feel that I am not as good a person as others because I have CF. 19 (42.2) 19 (42.2) 5 (11.1) 1 (2.2)
3. Having CF makes me feel unclean. 30 (66.7) 7 (15.6) 6 (13.3) 1 (2.2)
4. Having CF makes me feel that I’m a bad person. 37 (82.2) 6 (13.3) 1 (2.2)
5. Most people think that a person with CF is disgusting. 25 (55.6) 13 (28.9) 6 (13.3)
6. Most people with CF are rejected when others find out. 23 (51.1) 19 (42.2) 2 (4.4)
7. I have been hurt by how people reacted to learning I have CF. 22 (48.9) 11 (24.4) 2 (4.4) 1 (2.2)
8. I have stopped socializing with some people because of their reactions to my having CF. 23 (51.1) 13 (28.9) 7 (15.6)
9. I have lost friends by telling them I have CF. 27 (60.0) 15 (33.3) 2 (4.4)
10. I worry that people who know I have CF will tell others. 23 (51.1) 15 (33.3) 4 (8.9) 2 (4.4)

Note: Higher agreement reflects higher stigma experienced by patient

Reference

  • 1.Pakhale S, Armstrong M, Holly C, et al. Assessment of stigma in patients with cystic fibrosis. BMC Pulm Med. 2014;14:76. doi: 10.1186/1471-2466-14-76. [DOI] [PMC free article] [PubMed] [Google Scholar]

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