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01.12.2012 | Research article | Ausgabe 1/2012 Open Access

BMC Infectious Diseases 1/2012

Risk factors, microbiological findings and outcomes of necrotizing fasciitis in New Zealand: a retrospective chart review

Zeitschrift:
BMC Infectious Diseases > Ausgabe 1/2012
Autoren:
Dilip Kumar Das, Michael G Baker, Kamalesh Venugopal
Wichtige Hinweise

Competing interests

All the authors declare that that they have no competing interests.

Authors’ contributions

DD did the literature review, conducted the hospital chart review and analysis of resulting data, interpreted data, drafted the initial study report and wrote the final report. MB conceptualized the study and formulated the study design, and contributed to data interpretation. He revised and edited the manuscript. KV did the statistical analysis and contributed to data interpretation. He revised the manuscript. All authors read and approved the final manuscript.
Abbreviations
COPD
Chronic obstructive pulmonary disease
GAS
Group A streptococcus
ICD
International Classification of Diseases
ICU
Intensive care unit
IVDU
Intravenous drug use
MRSA
Methicillin-resistant Staphylococcus aureus
NF
Necrotizing fasciitis
NHI
National Health Index
NSAID
Non-steroidal anti-inflammatory drugs
NSTI
Necrotizing soft tissue infections
NZ
New Zealand
US
United States.

Background

Necrotizing fasciitis (NF) is a rapidly progressive soft tissue infection characterized by necrosis of the subcutaneous tissue and fascia [ 1, 2]. Although rare, NF frequently causes severe illness resulting in death or permanent disability [ 2]. Analysis of hospitalization data in New Zealand (NZ) for the period 1990 to 2006 showed that incidence and mortality rates of NF have increased significantly and the incidence is significantly higher in Pacific people and Maori than in Europeans and people of Other ethnicity [ 3]. The causes of the increase and differential ethnic distribution in incidence are not known [ 3].
The pathogenesis of NF involves a complex interplay between agent and host factors. Most patients who develop NF have pre-existing conditions that render them susceptible to infection [ 4], although it also occurs in young, previously healthy individuals [ 2, 5]. The disease occurs more frequently in the elderly [ 4, 6, 7], diabetics [ 4, 610], alcoholics [ 68], intravenous drug users [ 2, 4, 6, 11], in patients with chronic liver disease [ 2], renal insufficiency [ 4, 7, 8], peripheral vascular disease [ 4, 6, 7], gout [ 8, 12], underlying malignancy [ 4, 6, 7] or immunocompromised states [ 4, 6]. Other factors which have been found to be associated with NF are obesity [ 4, 6], malnutrition [ 4, 6], chronic obstructive pulmonary diseases [ 7, 9] and congestive heart failure [ 9]. Many NF patients are found to be taking non-steroidal anti-inflammatory drugs (NSAID) at the time of presentation to hospital [ 9, 12, 13], but its role remains unclear [ 14, 15].
Usually the disease is precipitated by some form of injury or local pathological condition [ 7]. Blunt or penetrating trauma [ 4], operation site infection [ 4], burn [ 4], ulcers [ 16], abscess [ 16] and even child birth [ 4] have been documented as precipitating factors for NF. Body piercing procedures such as acupuncture [ 6] and tattooing [ 17], very minor trauma such as abrasion [ 16] and insect bites [ 16] have also been found to initiate NF. In some situations NF has arisen without identifiable antecedent trauma [ 7, 16] or pathological state [ 7].
Tattooing and skin piercing are invasive procedures and can have infective complications if not done in a sterile way [ 18, 19]. A few cases of NF and severe soft tissue infection following traditional Samoan tattooing have been reported in NZ [ 17, 20] drawing wide media attention [ 21].
NF may be caused by a variety of aerobic and facultative anaerobic bacteria, including Streptococcus pyogenes or group A streptococci (GAS), Staphylococcus aureus, Escherichia coli, Clostridium and Bacteroides species [ 1]. Rarely, group B, C, and G streptococci, Haemophilus influenzae type b, Pseudomonas aeruginosa, Vibrio vulnificus, and fungi are involved [ 1]. Frequently the disease is polymicrobial [ 16, 22]. The microbiology of NF in NZ has not been well documented.
Managing NF uses a large amount of health-care resources [ 23]. It can also cause serious complications [ 23], such as acute renal failure, shock, multi-organ dysfunction, coagulopathy, arrhythmia, and myocardial infarction. Its management requires intensive care unit (ICU) admission in many cases, and urgent surgical debridement and intravenous antibiotics in almost all cases [ 1, 2, 24]. Many patients who survive require reconstructive surgery and skin grafting (often with multiple admissions) [ 25]. Blood product transfusion and dialysis are also needed to manage specific complications. The disease is associated with a high case fatality risk and permanent disability in the form of limb loss [ 26].
We conducted a retrospective chart review to investigate the relationship between the incidence of NF in NZ and traditional Samoan tattooing and other risk factors, and to document the microbiology, complications, treatment and outcomes of NF. A particular focus was to compare these characteristics across ethnic groups.

Methods

To explore the role of traditional Samoan tattooing in NF, we purposely selected hospitals with NF patients of Pacific ethnicity for chart review. From Ministry of Health hospital discharge data for the period 2000–2006, we identified hospitals where at least one person of Pacific ethnicity was admitted with NF during this period. These hospitals were: Auckland City, Starship, North Shore, Middlemore, Tauranga, Rotorua, Hutt and Wellington. These hospitals included 58% of the 513 cases discharged from NZ hospitals with an NF diagnosis over that seven year period.
By using the International Classification of Diseases (ICD) codes of NF (M7250 to M7269 in ICD-10-AM versions 1, 2 and 3) we identified the National Health Index (NHI) numbers of all NF patients (all ethnicities) in these hospitals admitted between 2000 and 2006 and subsequently located their charts.
One investigator (DD) visited Medical Records Departments of the above mentioned hospitals and extracted relevant data from patients’ charts and entered these into a Microsoft Access database.
A case was included in the chart review if it satisfied the following criteria:
  • Discharge diagnosis of NF (M7250 – M7269 in ICD-10), irrespective of whether NF was the principal diagnosis or an additional diagnosis; AND
  • Operation notes clearly indicated presence of necrosis in the fascia and subcutaneous tissue; OR
  • Operative finding specifically mentioned ‘necrotizing fasciitis’; OR
  • Histopathology of debrided fascia and subcutaneous tissue or autopsy findings of local tissue showed necrosis.
If the case has been coded as ‘NF’ or as ‘Fasciitis, Not Elsewhere Classified,’ but the operative or histopathology or autopsy criteria were not satisfied, the chart was not reviewed further.
We checked the data for any inconsistencies and outliers and corrected these in the data preparation stage. Frequency tables of variables of interest were generated. Tests of statistical significance were done using the Chi-square test. We used level 1 prioritized ethnicity and four ethnic groupings: European, Maori, Pacific and Other (including Asian) [ 27]. Data were analyzed using Statistical Package for the Social Sciences for Windows version 9 (SPSS Inc., Chicago, IL) and Epi Info™ version 6 (Centers for Disease Control and Prevention, Atlanta, GA).
Multi-Region Ethics Committee approval was obtained to access, review and extract the relevant data from NF patients’ charts from the selected hospitals.

Results and discussion

Patients included

We reviewed 299 NF patient charts of which 247 (82.6%) satisfied the case inclusion criteria. Conditions like diabetic gangrene of toe, foot and leg, cellulitis, abscess, plantar fasciitis, Dupuytren’s contracture, and limb loss due to invasive meningococcal disease were sometimes coded as fasciitis or NF. However, these were clearly not cases of NF and were excluded from the analysis. Operative and histology findings criteria were the two most commonly used criteria for assigning disease status. However, for more than half of the charts a histology report was not available. Many operative notes did not mention specific operative findings but just mentioned ‘NF found at operation’. Consequently, a very tight case definition could not always be applied.

Demography of reviewed patients

Table 1 shows the age, sex and ethnicity distribution of the 247 NF cases fulfilling the case definition. Males comprised 61% and females 39% of the total. Amongst Europeans the highest number of cases was in the 70+ age group, while for Maori and people of Pacific and Other ethnicity, the number of cases was highest in the 50–69 year age group. The median age of European cases (61.4 years) was significantly higher than Maori (48.9 years) and Pacific (50.8 years) (p < 0.001).
Table 1
Age, sex and ethnicity distribution of NF patients reviewed
Age group (years)
European (n=122)
Maori (n=47)
Pacific (n=60)
Others (n=17)
Total* (n=247)
 
M
F
M
F
M
F
M
F
M
F
0-14
2
1
1
2
2
1
0
0
5
4
15-29
3
3
5
3
5
3
0
2
13
11
30-49
17
11
11
5
13
5
2
2
43
23
50-69
25
15
10
7
14
11
7
2
56
35
70+
24
21
2
1
5
1
1
1
32
24
Total*
71
51
29
18
39
21
10
7
150
97
(%)
(58.2)
(41.8)
(61.7)
(38.3)
(65.0)
(35.0)
(58.8)
(41.2)
(60.7)
(39.3)
M – Male, F – Female. *Total includes one male case with ‘unknown’ ethnicity.

Predisposing conditions

Table 2 shows the ethnic distribution of selected predisposing conditions. Diabetes was the most common (32.0%) predisposing condition, followed by obesity (22.7%). Nearly a quarter of the patients (23.1%) were reported to have taken NSAID within the seven days preceding development of NF. About a fifth of the patients did not have any predisposing condition recorded in their charts.
Table 2
Presence of known predisposing conditions for NF by ethnicity
Predisposing conditions
European (n=122)
Maori (n=47)
Pacific (n=60)
Others (n=17)
Total (n=247)
p-value
 
No.
%
No.
%
No.
%
No.
%
No.
%
 
Diabetes mellitus
28
23.0
14
29.8
27
45.0
10
58.8
79
32.0
0.002
Alcohol abuse
11
9.0
3
6.4
0
0.0
1
5.9
15
6.1
0.126
Obesity
23
18.9
16
34.0
14
23.3
3
17.6
56
22.7
0.193
Coronary heart disease
22
18.0
8
17.0
5
8.3
5
29.4
40
16.2
0.156
Congestive heart failure
15
12.3
6
12.8
10
16.7
2
11.8
33
13.4
0.865
Peripheral vascular disease
14
11.5
6
12.8
4
6.7
2
11.8
26
10.5
0.720
Chronic obstructive
16
13.1
4
8.5
2
3.3
0
0.0
22
8.9
0.086
pulmonary disease
                     
Cancer
12
9.8
3
6.4
1
1.7
2
11.8
18
7.3
0.210
Chronic renal failure
11
9.0
9
19.1
7
11.7
2
11.8
29
11.7
0.341
Steroid use
14
11.5
2
4.3
1
1.7
0
0.0
17
6.9
0.040
Non-steroidal anti-inflammatory drug use*
29
23.8
11
23.4
10
16.7
7
41.2
57
23.1
0.208
No condition documented
18
14.8
10
21.3
20
33.3
0
0.0
49
19.8
0.004
*Low-dose Aspirin 100mg/day or less excluded.
Some conditions were comparatively more prevalent in particular ethnic groups, e.g., diabetes in Others and Pacific people, alcohol abuse in Europeans, obesity in Maori and Pacific people, coronary heart disease in Others, congestive heart failure in Pacific people, chronic obstructive pulmonary disease (COPD) in Europeans, cancers in Others and Europeans, steroid use in Europeans, NSAID use in Others and chronic renal failure in Maori. However, the ethnic difference in prevalence was significant only for diabetes (p < 0.01) and steroid use (p < 0.05). P-values in this and subsequent tables should be interpreted with caution where some cells have values <5. There was also a statistically significant difference (p 0.004) in the ethnic distribution of cases with ‘no condition documented’ (Table 2). From the available clinical notes it is not possible to say the cause of this association. The significantly greater age of the European cases may have contributed to the higher documented prevalence of co-morbidities for NF cases from that ethnic group.

Precipitating events

The distribution of precipitating events by ethnicity is shown in Table 3. By far the most commonly reported precipitating event was accidental trauma (33.2%), followed by skin ulcer (15.8%) and surgery (11.3%). The type of trauma ranged from superficial graze to blunt trauma without skin break, laceration and penetrating injuries. This group also included insect and animal bites. Five patients had a history of insect bite (one mosquito, one sand fly and three unspecified insect bites) as precipitating events. One person developed NF following a dog bite on their leg.
Table 3
Presence of precipitating events for NF by ethnicity in reviewed patients
Precipitating events
European (n=122)
Maori (n=47)
Pacific (n=60)
Others (n=17)
Total (n=247)
p-value
 
No.
%
No.
%
No.
%
No.
%
No.
%
 
Traditional tattooing
0
0.0
0
0.0
4
6.7
0
0.0
4
1.6
0.005
Accidental trauma
43
35.2
15
31.9
19
31.7
4
23.5
82
33.2
0.791
Skin ulcer
20
16.4
9
19.1
5
8.3
4
23.5
39
15.8
0.289
Surgery
16
13.1
6
12.8
4
6.7
2
11.8
28
11.3
0.619
Burns
3
2.5
0
0.0
0
0.0
0
0.0
3
1.2
0.378
Current IVDU*
2
1.6
1
2.1
0
0.0
0
0.0
3
1.2
0.693
*IVDU= Intravenous drug use.
Only four patients (1.6% of the total) developed NF directly following traditional Samoan tattooing. All of them were Samoan and one of them died. Not surprisingly, the p value of this category indicates statistically significant ethnic differences in exposure to this precipitating event (Table 3). Two people (0.8%) were noted to have acupuncture in the affected area before developing NF.

Microbiology

Out of 247 NF patients’ charts reviewed, either debrided tissue, blood, aspirated fluid or wound swab culture results (in the form of hard copy or electronic laboratory reports) were available for 219. Another 19 patients had their culture results documented in their clinical notes but no laboratory reports were filed in their charts. Specimens were taken at operation (debrided tissue or swab) or preoperatively (blood, blister fluid or wound swab). In total, there were culture positive results from one or more specimens in 96% (228/238) patients. The extent of microbiology investigations and their documentation in different hospitals were not uniform. For example, the number of antibiotics against which a cultured organism was tested for susceptibility differed substantially from hospital to hospital and also within the hospital from case to case. We are not sure whether specimens were cultured for all possible organisms. For example, for many cases anaerobic culture reports were not available. Some reported specific anaerobic organisms isolated while some indicated that there was growth of mixed anaerobes. It is also important to note that a third of all patients received antibiotics before hospital admission and specimens for culture were taken. Table 4 is a list of organisms isolated either solely or in combinations, and their frequency of occurrence.
Table 4
Micro-organisms isolated from NF patients for whom culture results were available (n=238)
 
Count
Percentage
Organisms and characteristics:
   
· Gram positive cocci
   
Streptococcus pyogenes
98
41.2%
 Other streptococci spp.
42
17.6%
Staphylococcus aureus (SA)
76
31.9%
 Other staphylococci spp.
37
15.5%
 MRSA
8
3.4%
· Gram positive bacilli
   
Corynebacterium spp.
5
2.1%
· Mixed gram positive organisms
4
1.7%
· Gram negative bacilli
   
E coli
23
9.7%
Proteus spp.
8
3.4%
Klebsiella spp.
3
1.3%
Enterobacter spp.
2
0.8%
Serratia spp.
5
2.1%
Citrobacter spp.
1
0.4%
Pseudomona spp.
17
7.1%
Eikenella spp.
1
0.4%
Providencia spp.
1
0.4%
Vibrio spp.
1
0.4%
Stenotrophomonas spp.
2
0.8%
Hafnia spp.
1
0.4%
Aeromonas hydrophilia
1
0.4%
 Mixed gram negative bacilli
7
2.9%
· Anaerobes
   
Bacteroides spp.
11
4.6%
Prevotella spp
3
1.3%
Clostridium spp
2
0.8%
Preptostreptococcus spp.
1
0.4%
 Mixed anaerobes
29
12.2%
· Mixed bowel flora
4
1.7%
· Mixed skin flora
7
2.9%
· Fungus
   
Candida spp.
1
0.4%
The most common organism isolated was Streptococcus pyogenes (41.2%) either solely (20.6%) or in combination with other organisms (20.6%). Streptococci other than Streptococcus pyogenes, usually in combination with other organisms, were isolated in 17.6% cases. For most of the Streptococcus pyogenes isolates antibiotic susceptibility testing was not done. The culture reports mentioned that Streptococcus pyogenes was universally susceptible to Penicillin.
The second most common organism isolated was Staphylococcus aureus (31.9%). Most (88.0%) Staphylococcus aureus isolates were resistant to penicillins. Susceptibility to erythromycin and flucloxacillin was 89.8% and 88.6% respectively. Methicillin-resistant Staphylococcus aureus (MRSA) was cultured in 8 (3.4%) cases.
The ethnic distribution of patients affected by these two organisms and the antibiotic susceptibility results of Staphylococcus aureus to three common antibiotics (penicillin, erythromycin and flucloxacillin) are presented in Table 5. Although a higher percentage of Pacific people cultured Streptococcus pyogenes and Staphylococcus aureus, these ethnic differences were not statistically significant.
Table 5
Distribution of Streptococcus pyogenes and Staphylococcus aureus (SA) and antibiotic susceptibility pattern of SA by ethnicity
 
European
Maori
Pacific
Other
Total
p-value
 
No.
%
No.
%
No.
%
No.
%
No.
%
Streptococcus pyogenes
48 (n=117)
41.0
18 (n=45)
40.0
28 (n=59)
47.5
4 (n=17)
23.5
98 (n=238)
41.2
0.366
Staphylococcus aureus (SA)
33 (n=117)
28.2
12 (n=45)
26.7
25 (n=59)
42.4
6 (n=17)
35.3
76 (n=238)
31.9
0.224
SA susceptible to Penicillin
5 (n=32)
15.6
1 (n=12)
8.3
3 (n=23)
13.0
0 (n=6)
0.0
9 (n=73)
12.3
0.716
SA susceptible to Erythromycin
23 (n=29)
79.3
12 (n=12)
100.0
21 (n=22)
95.5
6 (n=6)
100.0
62 (n=69)
89.9
0.097
SA susceptible to Flucloxacillin
29 (n=31)
93.5
10 (n=11)
90.9
17 (n=22)
77.3
6 (n=6)
100.0
62 (n=70)
88.6
0.224

Complication, specific intervention and outcome

Many NF patients developed several complications and underwent specific interventions during their hospital stay. Table 6 shows the frequency and ethnic distribution of some complications (renal failure, shock, multi-organ dysfunction, coagulation abnormalities and myocardial infarction), specific interventions (surgical debridement, skin grafting, blood product transfusion, ICU admission and dialysis) and two specific outcomes (amputation and death). The ethnic differences in the extent of complications, interventions and outcomes were not statistically significant.
Table 6
Complications, specific interventions and outcomes of NF admission by ethnicity in reviewed patients
 
European (n=122)
Maori (n=47)
Pacific (n=60)
Other (n=17)
Total (n=247)
p-value
 
No.
%
No.
%
No
%
No.
%
No.
%
 
Renal failure
54
44.3
20
42.6
24
40.0
7
41.2
105
42.2
0.957
Shock
54
44.3
17
36.2
24
40.0
9
52.9
105
42.5
0.607
Multi-organ dysfunction
21
17.2
8
17.0
12
20.0
3
17.6
44
17.8
0.970
Coagulation abnormality
31
25.4
8
17.0
11
18.3
3
17.6
53
21.5
0.539
Myocardial infarction
5
4.1
1
2.1
4
6.7
1
5.9
11
4.5
0.705
ICU admission
73
59.8
20
42.6
35
58.3
10
58.8
138
55.9
0.225
Surgical debridement
109
89.3
44
93.6
53
88.3
16
94.1
223
90.3
0.739
Skin grafting
64
52.5
26
55.3
34
56.7
7
41.2
131
53.0
0.708
Blood product transfusion
64
52.5
17
36.2
25
41.7
9
52.9
115
46.6
0.203
Dialysis
8
6.6
5
10.6
7
11.7
1
5.9
21
8.5
0.618
Amputation
22
18.0
5
10.6
5
8.3
2
11.8
34
13.8
0.285
Death
33
27.0
8
17.0
12
20.0
5
29.4
58
23.5
0.443
This is the largest NF case-series so far reported and shows several important features of the risk factors, microbiology, and outcomes for this infection. Our analysis confirms the earlier finding of a positive association of NF with increasing age and with male sex [ 3]. More than 80% of patients had one or more recognized predisposing conditions. For Europeans and people of Other ethnicity, two common conditions were diabetes and NSAID use, while those for Maori and Pacific people were diabetes and obesity. Increasing rates of diabetes and obesity in Pacific people and Maori are well documented [ 28], and these trends could partly explain the increasing incidence of NF in recent years [ 3]. An association has been documented between NF and NSAIDs and there are plausible mechanisms by which NSAIDs might predispose to severe bacterial infection [ 14]. We found that nearly a quarter of patients had a history of NSAID use within the seven days preceding onset of symptoms. This finding is consistent with the results of two studies from Middlemore Hospital in Auckland [ 9, 12]. However, the definitive answer regarding the question of causation has not been resolved [ 14, 29]. As in other studies [ 16], we found that accidental trauma, surgery, ulcer, burn and intra venous drug use (IVDU) had triggered the process in some cases. A third of patients had an antecedent history of accidental trauma (including blunt trauma without a breach in the skin).
Traditional Samoan tattooing was documented as the precipitating event for NF in four Samoan men, one of whom died. There were no further details of the process of tattooing or infection control procedures recorded in the patient notes, so we cannot implicate any particular aspect of the procedure as contributing to the risk of developing the condition. It was reported in two charts that NF developed at the site of acupuncture. No further details were available. Although there was considerable media attention and publicity about the risks from traditional Samoan tattooing, this review found that the contribution from this exposure was fortunately small in relation to the overall burden of NF. This finding is consistent with the international literature which has reported only a few sporadic cases of NF following traditional tattooing [ 17, 30]. It is probable that some people developed less severe forms of infection (e.g. cellulitis) following traditional tattooing [ 20]. However, exploration of those outcomes was not part of this study.
We found that Streptococcus pyogenes, either singly or in combination with a staphylococcus or other organism, was the most frequent organism isolated in NF cases. Fifty-eight percent of culture positive cases in this group grew Streptococcus pyogenes or a non-Group A streptococcus. This finding is consistent with the microbiology findings of a case series of 198 necrotizing soft tissue infections (NSTI) in the US, where a streptococcus was isolated in 56% of cases [ 22]. Staphylococcus aureus including MRSA was cultured in more than a third of our reviewed cases for whom a microbiology result was available. This proportion is higher than that reported for the other series [ 9, 10, 12, 16, 22]. Only about 10% of staphylococci were MRSA (8 out of 76). A wide variation of the proportion of MRSA from NF patients has been reported [ 22, 3133]. Our result is near the lower end of this range [ 22, 33].
In addition to the above two major organisms, many others were cultured from reviewed NF patients. This result is consistent with the findings of the NSTI case series already mentioned, though the frequencies were different [ 22].
Proportions of Pacific people with Streptococcus pyogenes and Staphylococcus aureus positive culture are higher (though not significantly) than in all other ethnic groups. From this limited information, it appears that staphylococcus may be playing a bigger role in the pathogenesis of NF in NZ, particularly affecting Pacific people. This observation might partly explain the higher rates observed in Pacific people but needs further exploration to assess whether it is an important finding.
Our study documents the severe consequences of NF in terms of the high proportion with serious complications and death. We could locate only one other study reporting the extent of health care resource used to manage NF [ 23]. Although some studies reported the proportion of NF cases resulting in death, limb loss and ICU care, we could not locate any large study which reported complication rates and specific interventions to manage these as reported in this current paper.
Our study has important limitations. The NF patient records reviewed were confined to those admitted to a sample of NZ hospitals from 2000 to 2006, though it did include the majority of NF cases discharged over that seven year period. Consequently, it may not be possible to generalize our findings to all hospitals in NZ and to other time periods. This study was also limited to reviewing data on NF cases and did not include a comparison population. As a result, it is difficult to evaluate the significance of the risk factors which appeared to be associated with NF, such as diabetes and NSAID use. Our review of cases was limited to information recorded in patient notes, so is likely to underestimate the proportions of some characteristics, particularly predisposing conditions and precipitating events.

Conclusions

From the retrospective chart review results, we conclude that NF incidence and distribution is strongly influenced by the presence of various known predisposing conditions which compromise immunity, particularly in the elderly. Traditional Samoan tattooing and other body piercing procedures are not major causes. There is also potentially a contribution from changes in the virulence of the causative organisms, though we could not assess this potential factor with the data that were available.
The rising incidence of NF in NZ [ 3] also needs to be put in the wider context of a well documented increase in serious skin infections in children that is caused by similar bacteria [ 34]. The incidence of serious infectious diseases in general has risen significantly in NZ over the 20 year period from 1989 to 2008, as have ethnic and socio-economic inequalities [ 35]. These wider changes suggest that there may also be a contribution to NF from broad health determinants, such as disparities in income, housing conditions, and access to health services.
Given the rising incidence of NF in NZ and its severity, greater effort should be put into preventing this disease and improving the outcomes for those infected. Findings from this study suggest that high risk groups identified here should be the focus of attention. Patients over 50 years of age with important predisposing conditions (diabetes, obesity) should be alerted to this risk. In particular, they should take care to protect themselves from skin trauma and ulcers, and also ensure rapid assessment of skin infections if they develop. Further analytic studies (probably case–control) should be considered to quantify the importance of the risk factors identified here, particularly the role of pharmaceuticals such as NSAIDs, steroids, and other immune suppressive drugs.

Acknowledgements

We thank New Zealand Ministry of Health for funding this work, and for identifying the hospital-discharged patients with necrotizing fasciitis codes. We also thank Auckland, Bay of Plenty, Capital & Coast, Counties Manukau, Hutt Valley, Lakes and Waitemata District Health Boards for giving us access to selected patients’ hospital charts to review.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Competing interests

All the authors declare that that they have no competing interests.

Authors’ contributions

DD did the literature review, conducted the hospital chart review and analysis of resulting data, interpreted data, drafted the initial study report and wrote the final report. MB conceptualized the study and formulated the study design, and contributed to data interpretation. He revised and edited the manuscript. KV did the statistical analysis and contributed to data interpretation. He revised the manuscript. All authors read and approved the final manuscript.
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