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Table 6 Methods used for bacteria identification and to minimize contamination and prevalence, and type of bacteria identified

From: Could low grade bacterial infection contribute to low back pain? A systematic review

Studies and design

Biopsy: Method, site and no. of specimens

Methods to minimize contamination

Duration of culturing biopsy material

Bacteria identification methods

Culture-positive samples (n, %)

Organisms identified in positive cultures (%)

Subsequently made generic analysis of P. acnes species

Quality score

Albert [2] Cross-sectional

Open

All scalpels flamed before use as extra precaution

7 days with subsequent 1 day of subculture

Culture, PCR

28/61 (46%)

P. acnes : 86%

Analytical profile index biochemical analysis using Rapid ID 32A kit (bioMerieux) and PCR amplification of 16S rDNA

78

Disc material

Gram-positive cocci: 14%

Five specimens

Coagulase-negative (CN) staphylococci: 7%

Stirling [14] Cross-sectional

Open

Stringent aseptic precautions taken to minimise risk of contamination

7 days

Culture, serology

19/36 (53%)

P. acnes : 84%

Microscopy of Gram-stained smears of tissue samples

78

Disc material

CN staphylococci: 11%

Not stated

Corynebacterium propinquum: 5%

Stirling [17] Cross-sectional

Open

Not stated

7 days

Culture, serology

76/207 (37%)

P. acnes : 64%

Microscopy of Gram-stained smears of tissue samples

56

Disc material

CN staphylococci: 14%

Not stated

Propionibacteria: 10.5%

Agarwal [16] Cross-sectional

Open

Disc material retained in a closed sterile sample cup

5 days

Culture

10/52 (19.2%)

P. acnes : 70%

Not stated

78

Disc material

Peptostreptococci: 10%

Not stated

Staphylococci aureus: 10%

CN staphylococci: 10%

Arndt [9] Cross-sectional

Open

Disc structures stored in sterile syringes filled with physiological saline solution, care was taken to avoid contamination during conditioning process of biopsy

Blood agar, Drigalski agar: 24 h

Culture

40/83 (48.2%)

P. acnes : 45%

Not stated

67

Disc material

Polyvitex chocolate agar: 4 days

CN staphylococci: 40%

1 in 1st 25 disk replacements; 3 in following 58

Blood agar supplemented with hemin: 5 days

CN bacilli: 7.5%

Peptone glucose yeast broth: 10 days

Bactec Peds Plue bottle with fructooligosaccharide nutritional supplement: 7 days

Coscia [11] Cross-sectional

Open

Specimens were obtained sterilely immediately at the time of surgical excision

Cultured using extended duration incubation techniques (repeated subcultures up to several weeks duration)

Culture

16/30 (53.3%)

Staphylococcus: 36%

Not stated

78

Disc material

P. acnes : 18%

Not stated

Ben-Galim [10] Cross-sectional

Open

Samples are processed and cultured intraoperatively under stringent, sterile operating theatre conditions, culture mediums were warmed to room temperature before each operation

2 weeks

Culture

2/30 (6.7%)

CN staphylococci: 100%

Not stated

67

Disc material

Four pieces (disc material dissected into four pieces)

Fritzell [12] Cross-sectional

Open

Samples taken openly (no needle), all operations except for one were performed through a microscope with use of bipolar diathermy, assuring a very ‘dry’ operation field

Not applicable

PCR

(PCR)

(PCR)

Not stated

67

Disc material

2/10 (20%)

Bacillus cereus: 50%

Two – one from annulus fibrosus and one from nucleus pulposus

Citrobacterbraaki/freundi: 50%

Carricajo [13] Cross-sectional

Open

Obtained under aseptic conditions

One horse-blood agar, two chocolate PolyVitex agar: 10 days

Culture

12/54 (22%)

P. acnes : 17%

Not stated

67

One Schaedler medium: 20 days

Disc material, muscle, ligamentum flavum

Anaerobic streptococci: 8%

Three – muscle, ligamentum flavum, herniated intervertebral discs

Wedderkopp [15] Cross-sectional

Needle

Obtained with sterile technique

2 weeks

Culture

2/24 (8.3%)

Staph epidermidis: 50%

Not stated

67

CN staphylococci: 50%

Vertebral body

One – at site of Modic Type 1 change