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Table 1 Baseline characteristics and pre-operative variables

From: Initial experience with a synthetic sealant PleuraSeal™ after pulmonary resections: a prospective study with retrospective case matched controls

Variablea

Overall

PleuraSeal™ Group

Control Group

p-valueb

 

40

20

20

 

Age (yrs.), mean (SD)

69 (45-82)

66 (47-81)

0.34

Gender

Male

31 (77%)

14 (70%)

17 (85%)

 

Female

9 (22%)

6 (30%)

3 (15%)

0.45

Chronic lung disease

22

11

11

 

COPD

19 (47%)

9 (45%)

10 (50%)

 

Lung emphysema

2 (5%)

2 (10%)

0 (0%)

 

Asthma

1 (2%)

0 (0%)

1 (5%)

0.58

Pulmonary function c

FEV1 actual (Ø %), mean (SD)

85.5 (17.9)

87 (20.2)

84 (15.6)

0.51

FEV1 predicted (Ø %), mean (SD)

65.5 (16.2)

69 (17.6)

62 (14.8)

0.18

DLCO actual (Ø %), mean (SD)

70.5 (14.5)

70 (15.7)

71 (13.3)

0.84

DLCO predicted (Ø %), mean (SD)

55 (14.6)

56 (16.3)

54 (12.9)

0.55

Neoadjuvant therapy

1

0

1

 

Radiation

0 (0%)

-

-

NA

Chemotherapy

1 (2%)

0 (0%)

1 (5%)

1.00

Concomitant disease

23

14

9

 

Diabetes

7 (17%)

4 (20%)

3 (15%)

1.00

Othersd

16 (40%)

10 (50%)

6 (30%)

0.23

Smoking behaviour

Current Smoker

15 (37%)

8 (40%)

7 (35%)

 

Ex smoker (≥12 month)

13 (32%)

6 (30%)

7 (35%)

 

Never smoked

12 (30%)

6 (30%)

6 (30%)

0.14

  1. aNumbers in percentage were rounded up were indicated.
  2. bContinuous variables were compared between groups by Students' t-test. Categorical variables were compared using two-sided Fisher's Exact test..
  3. cPreoperative pulmonary function test and postoperative variables based on amount of lung resection; FEV1: Forced expiratory volume (1 sec); DLCO: CO volume-adjusted diffusion capacity). Data shown in % of total function and as mean with SD where indicated; SD standard deviation.
  4. dOther entities: hypertension, cardiac insufficiency, arrhythmia absoluta