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Table 1 Adult cystic fibrosis patient demographics from those with isolated Pneumococcus cultures

From: Prevalence and impact of Streptococcus pneumoniae in adult cystic fibrosis patients: a retrospective chart review and capsular serotyping study

Patient

Agea

Sex

Mutation 1

Mutation 2

BMIb

FVC (L)c(% predicted)

FEV1(L)d(% predicted)

Pancreatic sufficient

Smoker status

CF Co-morbidities

Chronic pathogense

1

30

M

M1101K

M1101K

21.87

1.62 (35)

0.76 (20)

N

N

N

PA, SA, HI, Bcc

2

23

M

F508del

M1101K

16.05

3.29 (61)

0.94 (20)

N

N

Liver disease

PA, SA

3

30

F

F508del

P67L

32.03

N/A

N/A

Y

Y

N

SA

4

28

M

F508del

F508del

18.23

3.75 (68)

2.42 (54)

N

N

Sinus

PA, Bcc

5

29

F

F508del

F508del

15.58

2.06 (53)

1.08 (32)

N

N

CFRD, Sinus

PA

6

24

M

F508del

D110H

24.38

7.57 (140)

5.98 (128)

Y

Y

N

HI

7

24

M

F508del

F508del

16.20

3.77 (73)

1.4 (32)

Y

N

Sinus

PA

8

30

M

3659delC

394delTT

18.79

3.95 (75)

1.80 (41)

N

Y

Liver disease

PA

9

28

M

F508del

F508del

21.20

6.1 (117)

4.3 (100)

N

N

N

PA, SA

10

23

M

F508del

G551D

20.1

5.08 (88)

3.55 (74)

N

N

Sinus

PA, SA

11

30

F

F508del

Unknown

19.0

1.58 (35)

1.08 (29)

N

N

CFRD

PA

12

18

M

F508del

G178R

20.8

4.04 (107)

3.01 (86)

N

Y

Arthropathy, Sinus

SA, HI

13

28

F

F508del

F508del

19.7

2.48 (73)

1.5 (51)

N

N

N

PA

14

40

F

F508del

F508del

25.4

4.45 (134)

3.08 (110)

N

Y

CFRD, Arthropathy

PA, HI

15

22

M

F508del

F508del

21.7

4.26 (85)

2.94 (68)

N

N

Arthropathy

PA, SA

  1. aAge at time of first isolation of S. pneumoniae.
  2. bBMI: body mass index.
  3. cFVC: forced volume capacity, defined as an average of two values in the year preceding time of pneumococcus isolation.
  4. dFEV1: forced expiratory volume, defined as an average of two values in the year preceding time of pneumococcus isolation.
  5. ePA: P. aeruginosa, SA: S. aureus, HI: Haemophilus influenzae, Bcc: Burkholderia cepacia complex; chronicity as defined by repeated isolation of pathogen on at least 50% of cultures over the prior two years.