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Alain Dupuy a Dermatology Department, Hôpital Henri
Mondor, 94010 Créteil, France, b Public Health
Department, Hôpital Henri Mondor, c Dermatology Department,
Hôpital Robert Debré, 51092 Reims, France, d Dermatology Department,
Hôpital Trousseau, 37044 Tours, France, e Dermatology Department, Hôpital
Pitié-Salpêtrière, 75013 Paris, France, f Dermatology Department, Centre
Hospitalier Universitaire de Brest, 29285 Brest, France, g Dermatology Department,
Hôpital Pasteur, 68024 Colmar, France, h Dermatology Department, Hôpital
Sainte-Marguerite, 13009 Marseille, France
Correspondence to: Dr Bastuji-Garinsylvie
bastuji-garin{at}hmn.ap-hop-paris.fr
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Abstract |
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Objective:
To assess risk factors for erysipelas of
the leg (cellulitis).
Design:
Case-control study.
Setting:
7 hospital centres in France.
Subjects:
167 patients admitted to hospital for
erysipelas of the leg and 294 controls.
Results:
In multivariate analysis, a disruption of the cutaneous barrier (leg ulcer, wound, fissurated toe-web intertrigo, pressure ulcer, or leg dermatosis) (odds ratio 23.8, 95% confidence interval 10.7 to 52.5), lymphoedema (71.2, 5.6 to 908), venous insufficiency (2.9, 1.0 to 8.7), leg oedema (2.5, 1.2 to 5.1) and being
overweight (2.0, 1.1 to 3.7) were independently associated with
erysipelas of the leg. No association was observed with diabetes, alcohol, or smoking. Population attributable risk for toe-web intertrigo was 61%.
Conclusion:
This first case-control study highlights
the major role of local risk factors (mainly lymphoedema and site of
entry) in erysipelas of the leg. From a public health perspective, detecting and treating toe-web intertrigo should be evaluated in the
secondary prevention of erysipelas of the leg.
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Key messages
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Introduction |
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Commonly caused by streptococci, erysipelas is an infectious condition of the skin or subcutaneous tissue, which usually affects the leg (cellulitis).1-3 Although a potentially serious disease, erysipelas of the leg can be controlled with antibiotics. As recurrences of erysipelas are common and patients are usually admitted to hospital, cost is an important issue. The identification of risk factors for erysipelas is therefore critical in prevention of the disease.
Several factors, either local (for example, disruption of the cutaneous
barrier, lymphoedema, venous insufficiency) or general (for example,
diabetes mellitus, overweight, alcohol misuse), have been suspected as
risk factors for erysipelas of the leg from a few case
series.4-8 Owing to the inherent methodological limitations of such studies, however, these factors could not be
assessed quantitatively
that is, compared with a control group. We conducted a case-control sudy to assess risk factors for erysipelas of the leg, particularly the role of toe-web intertrigo and
other potential sites of entry.
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Subjects and methods |
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Study design
We conducted our case-control study prospectively from June 1995 to October 1996 in seven hospital centres in France. Cases and controls
were matched for age (range 5 years), sex, and hospital (admission
within the same 2 month period). For a type 1 error of 0.05%, 130 cases were sufficient to detect, with a power of 80%, odds ratios
>3.2 for factors with a prevalence of 5% in the general population
(for example, venous insufficiency) or odds ratios >2.5 for factors
with a prevalence of 10% in the general population (for example,
toe-web intertrigo).
Cases
We included patients admitted consecutively to each of the
participating centres for erysipelas of the leg. We excluded patients
under 15 years of age and patients with abscess or necrotising
fasciitis (defined by frank cutaneous necrosis on physical examination
or fascial oedema and necrosis detected at surgery). Erysipelas was
defined as the sudden onset (<24 hours) of a well demarcated cutaneous
inflammation, with fever >38°C or chills. Our definition for
erysipelas
that is, an acute bacterial dermohypodermatitis
corresponds to non-necrotising cellulitis in other
countries or reports. Of the 178 patients recruited, 11 (6%) did not
fulfil the inclusion criteria (8 had no fever or chills, and 3 had
cellulitis elsewhere). The 167 cases comprised 87 men (52%) and 80 women (48%) (mean age 56.5 (SE 1.8) years). The right leg was affected
in 85 cases (51%), the left in 78 (47%), and both in 4 (2%).
Overall, 129 patients (77%) were admitted for newly diagnosed
erysipelas of the leg, 8 (5%) for a first recurrence, 15 (9%) for a
second recurrence, and 15 (9%) for a third or more recurrence.
Controls
We included two controls for each case matched for age, sex, and
hospital, who were admitted for an acute condition not a priori related
to one of the suspected risk factors nor related to a chronic disease.
Among 323 potential controls, 21 (7%) were excluded because they did
not fulfil the above criteria. The 294 controls comprised 154 men
(52%) and 140 women (48%) (mean age 56.6 (1.1) years) who had been
admitted for trauma (109, 37%), dermatological conditions (49, 17%),
abdominal surgery (38, 13%), infection (30, 10%), orthopaedic surgery
(13, 4%), vascular disease (6, 2%), sciatalgia (6, 2%), eye disease
(2, 1%), and other conditions (41, 14%).
Data collection
One dermatologist in each centre conducted direct interviews with
a structured questionnaire and performed the clinical examination of
cases and controls. Besides age, sex, and current or past occupation,
we assessed general and local potential risk factors. General risk
factors included being overweight (>120% of the ideal weight as
calculated by Lorentz's formula), diabetes mellitus, smoking (current
smoker v non-smoker or past smoker), alcohol misuse (two
items on the CAGE questionnaire9), and seated position at
work. Local risk factors were a history of leg surgery, x
ray therapy (inferior limb or pelvis), neurological disorders, leg
thrombophlebitis, and leg ulcer. Leg oedema, lymphoedema, leg ulcer,
pressure ulcer, leg dermatosis, toe-web intertrigo, varicose veins or
varicosities, and peripheral pulses were detected by clinical
examination. No laboratory investigations were performed.
Data analysis
We compared both general and local factors between cases and controls.
whether or not
erysipelas was present. Toe-web interspaces were evaluated as: 1, normal; 2, doubtful; 3, abnormal; or 4, fissurated. We considered
intertrigo present with scores of 3 or 4 and absent with scores of 1 or 2.
In the analysis we included only cases with newly diagnosed erysipelas
of the leg (129 patients).10 We retained the controls matched to recurrent cases for the unconditional analysis but discarded
them for the conditional analysis. As the results of both analyses were
similar, we present only the results of the unconditional analysis.
We conducted a standard case-control analysis.10 For each
exposure we calculated odds ratios and 95% confidence intervals separately. We used unconditional logistic regression models and forced
the matching variables into all models. For lateralised factors, we
took into account only the ipsilateral side.
The factors we chose for inclusion in the multivariate model were
selected by using multiple 2 × 2 analyses on those variables that
emerged from the univariate analysis, and we assessed interaction and
confounding by fitting multiplicative models. We then conducted a final
backward step by step regression.
We conducted specific analyses for lateralised factors. These were
defined as local factors that could be present on a patient's limb yet
absent on the other
that is, history of phlebitis, leg ulcer, leg
surgery, neurological disorders, x ray therapy, current lymphoedema, abolition of a peripheral pulse, and site of entry (leg
ulcer, wound, pressure ulcer, excoriated leg dermatosis, toe-web
intertrigo). With the hypothesis that a lateralised factor
may be a site of entry if situated on the affected leg, we recorded
these factors as ipsilateral (affected side) or contralateral (healthy
leg) for cases. For controls, we arbitrarily determined an ipsilateral
and a contralateral side in each patient thus allowing comparisons
between cases and controls. We also compared ipsilateral and
contralateral sides in cases by paired analysis.
In the interests of public health, we calculated population
attributable risks as the fraction of the total disease experienced in
the population that would not have occurred if the effect associated with the risk factor was absent. This took into account adjusted odds
ratios and distribution of exposure among cases.11
We analysed the data with SAS-PC (version 6.12, SAS Institute, Cary,
NC) and BMDP software (University of California, Berkeley).
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Results |
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Risk factors for erysipelas of the leg
In the univariate analysis, seated position at work, diabetes
mellitus, alcohol misuse, and smoking were not associated with
erysipelas of the leg (table 1), and these were not further analysed.
We observed no association with a history of x ray therapy.
The associations between erysipelas of the leg and the presence of
either varicosities or a history of neurological disorders were close
to significance.
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Lateralised factors
The analysis comparing both legs among cases showed that all the
factors were more frequently present on the ipsilateral leg than on the
contralateral leg, and statistical significance was reached only for
history of phlebitis and history of x ray therapy (data not shown).
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Risks associated with the site of entry
Site of entry was a strong risk factor for erysipelas of the leg
(24.5; 11.0 to 54.9). We calculated multivariate estimates of odds
ratios and population attributable risks associated with each type of
site of entry. Leg ulcer (62.5; 7.0 to 556), toe-web intertrigo (13.9;
7.2 to 27.0), and traumatic wound (10.7; 4.8 to 23.8) exhibited strong
and highly significant associations with erysipelas of the leg whereas
pressure ulcer and excoriated leg dermatosis were not significant. The
strongest odds ratio was for leg ulcer, although the population
attributable risks associated with leg ulcer (14%) were much smaller
than for intertrigo (61%) or wound (35%).
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Discussion |
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To our knowledge this is the first controlled study to examine risk factors for erysipelas of the leg. In our study, diabetes and alcohol misuse were not associated with erysipelas of the leg, and being overweight was the only general factor associated with the condition. We showed that lymphoedema and a site of entry were the main risk factors. Among the different potential sites of entry, toe-web intertrigo had the highest population attributable risk.
Our study has some limitations. Firstly, because our study was hospital based the recruitment of cases could be biased toward more severe disease or more disabled patients. But because no community based study of erysipelas of the leg is available, it was impossible for us to assess whether our cases had more specific risk factors than those patients not referred to hospital. We only assessed patients from dermatology units, and in some hospitals not all cases of erysipelas of the leg are admitted to such units, so referral bias due to concurrent dermatological conditions may have occurred. We do not, however, believe that toe-web intertrigo was a reason for referring patients with erysipelas of the leg to a dermatology unit. Hospital controls were chosen for logistic reasons as we believe that non-inclusion of patients admitted to hospital for a chronic disease or for a disease that could have been a priori related to a suspected risk factor, and recruitment from different surgical or medical units, were sufficient for obtaining an appropriate control group.12
With regard to assessment of exposure and information bias, our investigators were dermatologists who knew whether subjects were controls or cases. The questionnaire, however, was standardised and did not contain open questions. Potential observer bias for assessment of toe-web interspaces was prevented by grouping the four categories in the questionnaire to two for the analysis.
Finally, major confounders were taken into account by matching factors and by adjustment during analysis. For lateralised factors, we controlled for confusion bias for presence or absence of a risk factor on the opposite leg by specific analyses.
Risk factors for erysipelas of the leg
Local factors seemed to be the most important risk factors for
erysipelas of the leg. Lymphoedema showed the greater risk, which was
present in 18% of our cases
more than in most,4
6 8 but not all,13 prior series.
Such a discrepancy may be due to the retrospective collection of data
in prior studies or to differences in the definition of lymphoedema or
lymphatic impairment. For most authors, lymphatic impairment plays a
major role in the pathophysiology of erysipelas of the
leg.1 13-15
Consequences in clinical practice
The major concern in long term clinical management of patients
with erysipelas of the leg is prediction and prevention of recurrences.
As we restricted the analysis, because of methodological concerns,10 to cases with newly diagnosed erysipelas of
the leg, we did not specifically study risk factors for recurrences. The prevalence of risk factors, however, was shown to be similar in
cases of recurrence and first episodes, and it can be reasonably assumed that a patient with strong risk factors for a first episode also has a strong risk for recurrence if these factors remained unchanged. The prevention of recurrence is currently based on long term
prophylactic antibiotherapy.18 19 Toe-web
intertrigo is highly prevalent in the population, and the high
population attributable risk of toe-web intertrigo in our study
suggests that suppression of this factor would result in a dramatic
decrease in incidence of erysipelas of the leg. The importance of
treating toe-web intertrigo has been previously
acknowledged20 21 but never assessed in a
quantitative way. In contrast to leg ulcers or traumatic wounds,
toe-web intertrigo is quite easy to avoid by detection and treatment.
We therefore suggest that screening for, and treatment of, toe-web
intertrigo should be a priority in subjects at high risk of erysipelas
of the leg or in whom avoidance of recurrences is critical. Whether
this strategy is sufficient alone or requires antibiotic prophylaxis
needs to be investigated.
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Acknowledgments |
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We thank the investigators who helped to collect the data: S Chauchaix (Tours), P M Dang (Limoges), H Dega (Paris), N Menard (Brest), and C Michel (Colmar). We thank L Mandereau for her help in the conditional analysis and P de La Salmonière for her critical review of the manuscript.
Contributors: All the authors, members of the RED (Réseau d'Epidémiologie en Dermatologie), participated in the protocol design, analysis, interpretation of the data, and writing of the paper. All of them, except AD and SB-G, recruited cases and controls. Furthermore, J-CR had the original idea for the present study and built the protocol design and questionnaire with SB-G. HB coordinated the seven participating centres, collected all the data, and set up the database. AD, under SB-G's supervision, conducted the statistical analysis, interpreted the data, and wrote the draft and the final version of the paper. SB-G will act as guarantor for the paper.
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Footnotes |
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Funding: None.
Competing interests: None declared.
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(Accepted 5 March 1999)
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