Main findings
Between 2017 and 2023, 53 patients were treated for necrotising soft tissue infection in the head and neck region at the Department of Otolaryngology, Oslo University Hospital, Rikshospitalet: 21 before the COVID-19 pandemic, 7 during and 25 after.
Group A streptococci were found in 8 of 21 patients in the pre-pandemic period and 18 of 25 in the post-pandemic period. All group A streptococcal isolates were susceptible to penicillin.
Necrotising soft tissue infections are severe and potentially fatal bacterial infections of the skin and soft tissues. Patients with comorbidities such as diabetes or immunodeficiency are particularly at risk (1, 2). There are no internationally accepted diagnostic criteria, and the nomenclature is ambiguous, as necrotising forms of cellulitis, fasciitis and myositis are all encompassed by the term (3). The absence of clear diagnostic criteria complicates comparisons across studies, but an incidence of 2–5 per 100,000 population per year has been reported in Scandinavia (1).
Necrotising soft tissue infections are characterised by a rapidly progressing clinical course that typically requires intensive care, surgery and antibiotics. The bacteria enter the soft tissue through broken skin or a mucosal barrier, either spontaneously or in connection with trauma or medical procedures (4, 5). The pathophysiology involves potent bacterial toxins that induce a cytokine storm, followed by impaired microcirculation, bacterial invasion of multiple tissue layers, ischemia and necrosis (4, 6).
Since the COVID-19 pandemic, international reports have indicated an increase in necrotising soft tissue infections overall, and particularly in cases caused by Streptococcus pyogenes (group A streptococci, GAS) (7–9). Invasive group A streptococcal infections are notifiable diseases in Norway, and national MSIS data have shown a post-pandemic increase (10).
The aim of our study was to investigate the incidence, aetiology and antimicrobial resistance patterns of necrotising soft tissue infections in the head and neck region in patients treated at the Department of Otolaryngology, Oslo University Hospital, Rikshospitalet, in the period 2017–23.
Material and method
The study was a retrospective review of patients treated for necrotising soft tissue infection at the Department of Otolaryngology in the period 1 January 2017 to 31 December 2023. Patients with a discharge diagnosis of M72.6 Necrotising fasciitis (ICD-10) were identified from electronic patient records. Inclusion criteria were the need for intensive care and at least one of the following perioperative findings: fat necrosis, poorly demarcated tissue layers with pus formation, necrotic oedema ('dishwater' fluid), microthrombosis, fascial thickening and nonviable muscle tissue. The COVID-19 pandemic period was defined as 12 March 2020 to 12 February 2022 (11).
Data collected included age, sex, comorbidities, body mass index, date of symptom onset and hospital admission, blood test results, microbiological findings and antimicrobial therapy.
The study was approved by the data protection officer at Oslo University Hospital as a quality assurance project. It was submitted to the Regional Committee for Medical and Health Research Ethics, which determined that prior review was not required.
Results
Sixty-six patients were identified, of whom 53 met the inclusion criteria and were included in the study: 21 patients (40 %) were treated for necrotising soft tissue infection pre-pandemic, 7 (13 %) during and 25 (47 %) post-pandemic (Table 1). During the study period, an average of 0.6 patients were treated per month. The monthly average was 0.5 pre-pandemic, 0.3 during the pandemic and 1.1 post-pandemic.
Bacterial growth in pus was found in 48 patients (91 %), and eight patients (15 %) had a positive blood culture. Patient characteristics and bacterial findings are summarised in Table 1.
Group A streptococci were identified in blood cultures or from pus/tissue fluid from the surgical site in 27 patients (51 %) (Figure 1). Other microbes were found in an additional 23 patients: Streptococcus constellatus (n = 11), Streptococcus anginosus (n = 6), Cutibacterium acnes (n = 2), Haemophilus influenzae (n = 2), Staphylococcus epidermidis (n = 1) and Staphylococcus aureus (n = 1).
All group A streptococcal isolates were susceptible to penicillin. In the period 2017–2022, the most common antibiotic regimen was a combination of cefotaxime, clindamycin and metronidazole, while in 2023 most patients received piperacillin–tazobactam and clindamycin (Figure 2).
Discussion
Among patients treated for necrotising soft tissue infection in the head and neck region at Rikshospitalet, group A streptococci were isolated in 18 of 25 during the nearly two years following the COVID-19 pandemic, compared with 8 of 21 in the approximately three years preceding the pandemic. Several countries have reported a post-pandemic increase in the incidence of necrotising soft tissue infections (7–9), including Sweden, where infection control measures were less restrictive than in Norway (7, 9).
The cause of this increase remains unclear, but possible contributing factors include reduced herd immunity to group A streptococci due to lower exposure during the pandemic, changes in bacterial virulence factors and increased susceptibility to bacterial infections following COVID-19 infection (12–14).
Beta-lactam resistance in group A streptococci is extremely rare. As all strains in our study were susceptible to penicillin, resistance development does not appear to explain the post-pandemic hospitalisations for necrotising soft tissue infections. No clindamycin-resistant group A streptococci were found in our material. In light of the 2023 NORM report, which documented 2.9 % clindamycin resistance among 382 blood culture isolates, we consider this a minor issue in the context of clinical empirical treatment (15). In December 2022, the national guidelines for antibiotic use in hospitals were revised, recommending piperacillin–tazobactam and clindamycin for severe soft tissue infections in the head and neck region (16). Antibiotic use at our department was in line with current guidelines throughout the study period.
In terms of age, sex and comorbidity, we found no obvious variation among patients before, during or after the pandemic (Table 1). In South-Eastern Norway Regional Health Authority, patients with necrotising soft tissue infections of the head and neck are primarily treated at the Department of Otorhinolaryngology, Oslo University Hospital, Rikshospitalet. During the relatively short study period, no changes were made to the catchment area or referral procedures, nor were any new diagnostic criteria established. It is therefore unlikely that the results were influenced by changes in clinical practice or patient selection.
The study's limitations include its retrospective design and reliance on data extracted from unstructured patient records. Data were limited to the South-Eastern Norway Regional Health Authority catchment area, and there were therefore few patients in each period. Consequently, no conclusions can be drawn regarding changes in incidence, and the results should be interpreted with caution. We believe the findings are, nevertheless, interesting. To the best of our knowledge, no other data have been published on this patient group in Norway during the same period, and the medical community has called for further studies on this population (6).
Even after intensive and comprehensive treatment, patients with necrotising soft tissue infections experience significant morbidity and mortality. National prospective studies, involving collaboration across health regions, medical specialties and expert groups, are needed to improve understanding of the aetiology, refine diagnostics and develop more effective treatment for these severely ill patients.
The article has been peer-reviewed.
- 1.
Hedetoft M, Madsen MB, Madsen LB et al. Incidence, comorbidity and mortality in patients with necrotising soft-tissue infections, 2005-2018: a Danish nationwide register-based cohort study. BMJ Open 2020; 10. doi: 10.1136/bmjopen-2020-041302. [PubMed][CrossRef]
- 2.
Cheng NC, Tai HC, Chang SC et al. Necrotizing fasciitis in patients with diabetes mellitus: clinical characteristics and risk factors for mortality. BMC Infect Dis 2015; 15: 417. [PubMed][CrossRef]
- 3.
Stevens DL, Bryant AE. Necrotizing Soft-Tissue Infections. N Engl J Med 2017; 377: 2253–65. [PubMed][CrossRef]
- 4.
INFECT study group. Patient's characteristics and outcomes in necrotising soft-tissue infections: results from a Scandinavian, multicentre, prospective cohort study. Intensive Care Med 2019; 45: 1241–51. [PubMed][CrossRef]
- 5.
Shindo ML, Nalbone VP, Dougherty WR. Necrotizing fasciitis of the face. Laryngoscope 1997; 107: 1071–9. [PubMed][CrossRef]
- 6.
Gundersen IM, Bruun T, Almeland SK et al. Nekrotiserende bløtdelsinfeksjoner. Tidsskr Nor Legeforen 2024; 144. doi: 10.4045/tidsskr.23.0720. [PubMed][CrossRef]
- 7.
Breidung D, Billner M, Megas IF et al. Increase in Streptococcal Necrotizing Fasciitis During and After the Coronavirus Disease 2019 Pandemic. Surg Infect (Larchmt) 2024; 25: 169–74. [PubMed][CrossRef]
- 8.
WHO. Increased incidence of scarlet fever and invasive Group A Streptococcus infection – multi-country. https://www.who.int/emergencies/disease-outbreak-news/item/2022-DON429 Accessed 3.3.2025.
- 9.
WHO. Increase in invasive Group A streptococcal infections among children in Europe, including fatalities. https://www.who.int/europe/news/item/12-12-2022-increase-in-invasive-group-a-streptococcal-infections-among-children-in-europe--including-fatalities Accessed 3.3.2025.
- 10.
Valcarcel Salamanca B, Cyr PR, Bentdal YE et al. Increase in invasive group A streptococcal infections (iGAS) in children and older adults, Norway, 2022 to 2024. Euro Surveill 2024; 29. doi: 10.2807/1560-7917.ES.2024.29.20.2400242. [PubMed][CrossRef]
- 11.
FHI. Covid-19 - håndbok for helsepersonell covid-19 om sykdommen. https://www.fhi.no/sm/smittevernhandboka/sykdommer-a-a/covid-19/?term=-dagens-situasjon Accessed 5.3.2025.
- 12.
Gao F, Mallajosyula V, Arunachalam PS et al. Spheromers reveal robust T cell responses to the Pfizer/BioNTech vaccine and attenuated peripheral CD8+ T cell responses post SARS-CoV-2 infection. Immunity 2023; 56: 864–878.e4. [PubMed][CrossRef]
- 13.
Files JK, Boppana S, Perez MD et al. Sustained cellular immune dysregulation in individuals recovering from SARS-CoV-2 infection. J Clin Invest 2021; 131. doi: 10.1172/JCI140491. [PubMed][CrossRef]
- 14.
Johannesen TB, Munkstrup C, Edslev SM et al. Increase in invasive group A streptococcal infections and emergence of novel, rapidly expanding sub-lineage of the virulent Streptococcus pyogenes M1 clone, Denmark, 2023. Euro Surveill 2023; 28. doi: 10.2807/1560-7917.ES.2023.28.26.2300291. [PubMed][CrossRef]
- 15.
FHI. NORM NORM-VET 2023. Usage of Antimicrobial Agents and Occurrence of Antimicrobial Resistance in Norway. https://www.fhi.no/contentassets/4e24fb63a3754577a94c42b6c8cc89c4/norm-norm-vet-2023-komplett.pdf Accessed 20.7.2025.
- 16.
Helsedirektoratet. Antibiotika i sykehus. Nasjonal faglig retningslinje. Kap.15 Hud- og bløtdelsinfeksjoner. https://www.helsedirektoratet.no/retningslinjer/antibiotika-i-sykehus/hud-og-blotdelsinfeksjoner Accessed 3.3.2025.