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. 2019 Feb 20;12:469–480. doi: 10.2147/IDR.S186996

Table 4.

Description of participants treated with M&N scheme as first therapeutic option

Age (years) Site of HA injection HA volume (mL) Nodulediameter (cm) Time between HA injection and biofilm formation (months) Site affected by biofilm Relapse HA injection after recovery No biofilm relapse 2 years after recovery
48 Nasolabial folds, corners of mouth 1 ≤2 6 Right corner of mouth No Yes Yes
49 Tear troughs, nasolabial folds, lips 3 ≤2 4 All areas treated No Yes Yes
59 Tear troughs, cheeks, chin 6 ≤2 2 Right cheek No Yes Yes
31 Tear troughs 1 Orbital cavity 10 Right tear trough No Yes Yes
37 Nasolabial folds, corners of mouth, lips 2 ≤2 4 Right nasolabial fold No Yes Yes

Notes: Comprehensive treatment in accordance with the M&N scheme: puncture of the lesion and drainage of pus and fermented HA. Orally administered combination antibiotic and probiotic therapy: 2×400 mg moxifloxacin + 2×500 mg clarithromycin + probiotic formulation consisting of 1.6 billion CFU lyophilized strains of Lactobacillus acidophilus, L. delbrueckii subsp. bulgaricus, and Bifidobacterium lactis, three capsules a day. Duration of antibiotic therapy: 14–21 days or until the complete resolution of swelling and nodules (whichever is longer). Duration of probiotic treatment: during the antibiotic therapy and 1 month after its termination. Duration of locally administered hyaluronidase treatment: 14–21 days or until the complete resolution of swelling and nodules (whichever was longer). Hyaluronidase dosage: according to Table 2.

Abbreviations: M&N, Marusza and Netsvyetayeva; HA, hyaluronic acid; CFU, colony-forming unit.