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Table 1 Characteristics of the identified studies

From: High mortality in patients with Mycobacterium avium complex lung disease: a systematic review

Data set

Country and year

Diagnosis

N

Age (years)

Female sex (%)

NB (%)

FC (%)

NB + FC (%)

Unknown, unclassified or other (%)

Therapy

Five-year mortality rate (%) (95% CI)

Retrospective medical chart reviews

1

USA, 1973 [12]

MAC lung diseaseb

45

49% > 50

0

NR

81.0 (multiple cavities in 50%)

NR

11.0 (unknown)

1–3 drugs: 53%

≥4 drugs: 47%

Adjunctive surgical treatment: 42%

Duration: 5 years

40 (21.5–58.5)

2

Japan, 2012 [13]

Newly-diagnosed MAC lung disease

634

68.9 (mean) ± 11.4 (SD)

58.5

82.9

11.5

3.3

2.3 (unclassified)

First-line antibiotic therapy: 50.9%

Duration > 3 months

23.9 (20.1–27.7)

3

Japan, 2012 [14]

Newly diagnosed MAC lung disease

78

65.2 (mean) ± 12.6 (SD)

60.3

59.0 (bronchiectatic)

26.0

NR

NR

Various treatment regimens: 69%

Untreated: 31%

Duration NR

25.6 (14.4–36.8)

4

Japan, 2013 [15]

Rheumatoid arthritis and MAC lung disease

82

67.6 (mean) ± 10.3 (SD)

70.7

59.8

13.4

18.3

8.5

(other)

1 or 2 drug regimens,

Treatment for rheumatic disease

Duration > 3 months

32.8 (20.4–45.2)

5

Japan, 2014 [16]

MAC lung disease

309

67.0 (mean) ± 13.7 (SD)

64.7

NR

NR

NR

NR

Standard 3-drug regimen including clarithromycin: 131 patients (42.4%)

Duration > 6 months for 108 regimens.

Pulmonary resection: 5.1%

10.0 (6.8–13.1)

6

UK, 2014 [17]

Non-cystic fibrosis bronchiectasis and coexisting MAC infection

52

63.1 ± 12.7

69.2

NR

NR

NR

NR

NR

21 (8.5–33.5)

7

Japan, 2015 [18]

Nodular/ bronchiectatic MAC lung disease, based on HRCT of the chest

782

68.1 (mean) ± 11.1 (SD)

68.5

NR

15.0

NR

NR

First line antibiotic therapy, 1–5 drug regimen: 19.6%

Duration > 3 months

12.5 (10.0–15.0)

8

Japan, 2017 [19],a

MAC lung disease

368

72 (mean) ± 10 (SD)

59.0

81.0

11.1

1.6

9.5

165 treated patients; Clarithromycin + ethambutol + rifampicin (79.3%); other regimens (20.7%)

23 (17.7–27.3)

9

Japan, 2017 [19],a

MAC lung disease

118

70 (mean) ± 10 (SD)

55

85.6

11.9

0

2.5

66 treated patients; Clarithromycin + ethambutol + rifampicin (79.3%); other regimens (20.7%)

15 (7.8–21.6)

Retrospective population registry analyses

10

Denmark, 2010 [20]

Prevalent NTM-PD (MAC subgroup considered)

425

61.2 (mean) ± 16.5 (SD)

41.0

NR

NR

NR

NR

NR

39.7 (33.7–45.7)

11

Canada, 2017 [21]

MAC lung disease

5543

70 (median), IQR 50–78

53.0

NR

NR

NR

NR

NR

33.3 (31.8–34.8)

12

Japan, 2017 [22]

NTM-PD§

125

60 (median) IQR 49–66

66.0%

NR

NR

NR

NR

≥3 drug regimen including clarithromycin 76%; 2 drug regimen including clarithromycin 2%; clarithromycin monotherapy 4%; non-clarithromycin regimen 5%

16 (7.8–21.6)

13

USA 2017 [23],a

NTM-PD (meeting ATS/IDSA criteria) treated with pulmonary resection

178

66.1 (mean) ±14.6 (SD)

60

NR

NR

NR

NR

 

37 (27.6–45.4)

14

USA, 2017 [23],a

NTM-PD (not meeting ATS/IDSA criteria) treated with pulmonary resection

138

62.4 (mean) ±17.3 (SD)

51

NR

NR

NR

NR

NR

33 (23.7–43.0)

Prospective, randomized studies

15

UK and Scandinavia, 2002 [24]

MAC lung disease

75

64 (mean)

46.7

NR

61

NR

NR

Rifampicin +ethambutol ±isoniazid

Duration: 2 years

36.0 (22.4–49.6)

16

UK, Denmark, Sweden and Italy, 2008 [25],a

MAC lung disease

83

65 (mean)

51.8

NR

69

NR

NR

Rifampicin +ethambutol

+clarithromycin

±immunotherapy

Duration: 2 years

48.0 (33.1–62.9)

17

UK, Denmark, Sweden and Italy, 2008 [25],a

MAC lung disease

87

65 (mean)

49.4

NR

66

NR

NR

Rifampicin

+ethambutol

+ciprofloxacin

±immunotherapy

Duration: 2 years

30.0 (18.5–41.5)

  1. Studies are ordered within categories by year of publication
  2. ATS/IDSA American Thoracic Society/Infectious Diseases Society of America, CI confidence interval, FC fibrocavitary disease, HRCT high resolution computed tomography, IQR interquartile range, MAC Mycobacterium avium complex, NB nodular/bronchiectatic disease, NR not reported, NTM nontuberculous mycobacterium, PD pulmonary disease, SD standard deviation
  3. aMortality data were provided for two differently treated cohorts of patients with MAC lung disease. bPulmonary parenchymal disease by chest radiograph, sputum or bronchial wash containing M. intracellulare, physician’s opinion that M. intracellulare caused the disease. Disease fulfilled 2007 ATS/IDSA criteria. [2] §This study included primarily patients with MAC lung disease (86%) [22]. These data sets included primarily MAC lung disease patients (84% in full cohort, 89% of those meeting ATS/IDSA criteria [data set 13], 78% of those not meeting ATS/IDSA criteria [data set 14]) [23]. Sputum culture positive for MAC on at least two occasions separated by at least a week, radiographic changes compatible with mycobacterial pulmonary disease, and/or clinical evidence of such disease