Compartilhar
Informação da revista
Vol. 93. Núm. 5.
Páginas 755-758 (1 setembro 2018)
Compartilhar
Compartilhar
Baixar PDF
Mais opções do artigo
Vol. 93. Núm. 5.
Páginas 755-758 (1 setembro 2018)
Open Access
Seasonality of the hospitalizations at a dermatologic ward (2007-2017)*
Visitas
3901
Leonardo de Andrade Rodrigues Brito1, Ana Cláudia Mendes do Nascimento2, Carla de Marque1, Hélio Amante Miot3
1 Medical school student, Faculdade de Medicina de Botucatu, Universidade Estadual Paulista, Botucatu (SP), Brazil.
2 Dermatologic Clinic Ana Cláudia Mendes do Nascimento, Uberlândia (MG), Brazil.
3 Department of Dermatology and Radiotherapy, Faculdade de Medicina de Botucatu, Universidade Estadual Paulista, Botucatu (SP), Brazil.
Este item recebeu

Under a Creative Commons license
Informação do artigo
Resume
Texto Completo
Bibliografia
Baixar PDF
Estatísticas
Tabelas (2)
Table 1. Categories of dermatological diagnoses grouped by similarity
Table 2. Seasonal incidence of the diagnostic groups. In blue, the diagnoses that exceeded the expected frequencies for the season (p ≤ 0.05); in red, those that were less frequent (p ≤ 0.05)
Mostrar maisMostrar menos
Abstract

There is little data in the literature concerning dermatologic admissions. Several diseases are seasonal in incidence and clinical worsening. We performed a survey of hospitalizations in the dermatology ward of a public hospital (April/2007 to May/2017). There were 1790 hospitalizations, whose main diagnoses were infectious dermatoses, neoplasias, psoriasis, bullous diseases and cutaneous ulcers. In winter, there were fewer hospitalizations for bacterial infections and urticaria, but more for leprosy. In summer, there were fewer hospitalizations for systemic and subcutaneous mycoses, but more for zoodermatoses and erythema multiforme. In the fall, more patients were admitted with mycoses. Spring favored urticaria and angioedema, but less cases of erythema multiforme and diabetic foot.

Keywords:
Dermatology
Inpatient care units
Seasons
Texto Completo

Dermatologists practice predominantly in the outpatient setting but there are severe skin conditions that represent life risks or require admission for specialized treatment. However, there is limited data in the literature about skin conditions that might require hospital admission.1,2

As with some conditions (for example, asthma, influenza and depression), many skin disorders are seasonal in regards to their incidence or clinical worsening, such as actinic keratoses and melasma in summer, psoriasis and atopic dermatitis in winter, pityriasis rosea in spring, among others.3–5

Seasonality interferes in the course and efficacy of the treatment of certain conditions due to the pathophysiological basis of the disease, climatic temperature regimens and humidity or exposure to environmental triggers related to the astronomic season.6

Since hospital admissions are indicators of the severity of the dermatological clinical picture, investigation of seasonality of admissions reveals the profile of exacerbation or incidence, what generates relevant epidemiological data in collective health. The objective of this study was to explore the seasonality of groups of skin conditions that required admission into a public hospital in Brazil.

We conducted a retrospective study that analyzed data related to the admission of patients based on the registry of a dermatology ward of a public university service (Unesp, Botucatu, SP, Brazil; latitude: 22°53°09″S; longitude: 48°26°42″W; height: 804 m) between the months of April 2007 and May 2017.

Demographical and clinical characteristics were evaluated, as well as those related to the time of admission. The diagnoses were grouped into 21 categories (Table 1).

Table 1.

Categories of dermatological diagnoses grouped by similarity

Diagnostic group  Conditions 
Atopic dermatitis  Atopic dermatitis, hyper-IgE syndrome, gestational pruritus, atopic eczema 
Bacterial infection  Cellulitis, erysipelas, abscess, necrotizing fasciitis, syphilis 
Bullous disease  Pemphigus vulgaris, pemphigus foliaceous, bullous pemphigoid, dermatitis herpetiformis, Darier’s disease, Hailey-Hailey disease 
Contact dermatitis  Allergic or irritant contact dermatitis, contact dermatitis with secondary generalization, seborrheic dermatitis, stasis dermatitis, eczema, baboon syndrome 
Diabetic foot  Infectious and necrotic complications of the foot in diabetic patients 
Drug reactions  DRESS, TEN, drug-induced erythroderma 
Epithelial tumor  Basal cell carcinoma, squamous cell carcinoma, Merkel cell carcinoma, cutaneous melanoma, metastases, surgical complications of these tumors 
Erythema multiforme  Erythema multiforme, Stevens-Johnson syndrome, Sweet’s syndrome, pyoderma gangrenosum 
Herpes  Herpes-simplex virus infection (HSV), Kaposi varicelliform eruption, varicella, zoster 
Leprosy  Leprosy, type I and II reactions, erythema nodosum leprosum 
Leishmaniasis  American tegumentary leishmaniasis 
Lupus  Cutaneous and systemic lupus erythematosus, dermatomyositis 
Lymphoma  CTCL, B-cell lymphoma, large plaque parapsoriasis, lymphomatoid papulosis, mycosis fungoides 
Mycosis  Paracoccidioidomycosis, chromomycosis, sporotrichosis, cryptococcosis, histoplasmosis, mycetoma 
Phenol chemical peel  — (Admission for phenol chemical peel) 
Psoriasis  Psoriasis vulgaris, erythrodermic psoriasis, pustular psoriasis, subcorneal pustulosis, exfoliative erythroderma/of unknown cause 
Ulcer  Ulcer of the lower limbs: venous, arterial, mixed 
Urticaria  Urticaria, angioedema 
Vasculitis  Small, medium and large vessel vasculitis, livedoid vasculopathy, Behçet’s disease, Takayasu’s arteritis 
Zoonoses  Loxoscelism, insect bites, injuries with poisonous animals 
Others  Less common conditions (< 1%) 

Categorical variables were represented by percentage and compared by Chi-square and by the analysis of residues (standardized and adjusted) of the contingency table. Quantitative variables were represented by means and standard deviations or medians and quartiles (p25–p75) and compared with the Student’s T and Mann-Whitney tests, if indicated. We considered significant a value of p ≤ 0.05.

In total, 1790 dermatological admissions were evaluated in a period of 10.1 years, with 941 (53%) male patients. The mean age (sd) was 55 (19) years. The median (p25–p75) of the length of admissions was 9 (5–15) days. Men were older on admission [57 (19) years vs. 54 (20) years (p < 0.01)] and had longer length of hospital stay [10 (6–16) days vs. 8 (5–14) days (p < 0.01)].

Diagnoses were grouped into categories and evaluated according to seasonality of admissions (Table 2). The main reasons for admission (56%) were infectious conditions, epithelial neoplasms and psoriasis.

Table 2.

Seasonal incidence of the diagnostic groups. In blue, the diagnoses that exceeded the expected frequencies for the season (p ≤ 0.05); in red, those that were less frequent (p ≤ 0.05)

Diagnostic group  Summer*  Fall*  Winter*  Spring*  Total** 
Bacterial infection  121 (28)  128 (29)  75 (17)  111 (26)  435 (24) 
Epithelial tumor  53 (23)  72 (31)  51 (22)  59 (25)  235 (13) 
Psoriasis  30 (19)  46 (30)  41 (27)  38 (25)  155 (9) 
Ulcer  29 (30)  27 (28)  17 (17)  25 (26)  98 (5) 
Bullous diseases  27 (33)  16 (20)  21 (26)  17 (21)  81 (5) 
Lupus  22 (28)  25 (32)  15 (19)  16 (21)  78 (4) 
Contact dermatitis  18 (25)  20 (28)  14 (20)  19 (27)  71 (4) 
Drug eruptions  11 (16)  23 (34)  15 (22)  18 (27)  67 (4) 
Vasculitis  22 (33)  17 (26)  14 (21)  13 (20)  66 (4) 
Mycosis  6 (10)  24 (41)  17 (29)  12 (20)  59 (3) 
E. multiforme  19 (37)  18 (35)  8 (16)  6 (12)  51 (3) 
Leprosy  10 (20)  11 (22)  17 (35)  11 (22)  49 (3) 
Diabetic foot  14 (30)  16 (35)  12 (26)  4 (9)  46 (3) 
Herpes  9 (21)  8 (19)  14 (33)  11 (26)  42 (2) 
Leishmaniasis  6 (19)  8 (25)  11 (34)  7 (22)  32 (2) 
Lymphoma  3 (12)  9 (35)  7 (27)  7 (27)  26 (1) 
Phenol chemical peel  1 (5)  1 (5)  11 (50)  9 (41)  22 (1) 
Zoonoses  9 (53)  6 (35)  1 (6)  1 (6)  17 (1) 
Atopic dermatitis  4 (24)  3 (18)  5 (29)  5 (29)  17 (1) 
Urticaria  3 (21)  4 (29)  —  7 (50)  14 (1) 
Others  30 (23)  41 (32)  36 (28)  22 (17)  129 (7) 
Total  447 (25)  523 (29)  402 (23)  418 (23)  1790 (100) 

Chi square = 104; 60 gl; p < 0.01

Blue: p ≤ 0.05; higher than expect; red: p ≤ 0.05; lower than expected.

*

N (%) group;

**

N (%) total

Stays longer than 10 days were due to leprosy, leishmaniasis, ulcers, mycoses, diabetic foot, psoriasis, zoonoses and bullous diseases; stays shorter than 8 days were due to phenol peels, urticaria, lupus, vasculitis, contact dermatitis, erythema multiforme and tumors.

Of note, in winter there was a lower incidence of bacterial infections but a higher incidence of leprosy and admissions for deep chemical peels. In summer months, there was a lower incidence of deep mycoses but a higher incidence of zoonoses and erythema multiforme. Spring favored the incidence of urticaria and angioedema, with less frequent admissions for diabetic foot and erythema multiforme. In fall, more patients with mycoses were admitted.

Although not statistically significant (p = 0.09), there were less admissions for psoriasis and drug reactions in summer.

Twenty-six (1.5%) deaths were seen during admission. We highlight as causes: infectious diseases, neoplasms and bullous diseases, besides advanced age (older than 70 years).

This study identified groups of skin conditions that lead to admission associated to the seasons. The subtropical climate of the region studied, with well-defined seasons regarding temperature, sun exposure and rain, favors the investigation of which climatic, exposure or behavioral factors interfere in the incidence and severity of cutaneous diseases.

Hospital stay, prevalence of diagnosis and mortality patterns are similar to other case series.1,2

The skin, as a contact organ, is susceptible to the effect of environmental triggers for the development of diseases. Ultraviolet radiation has a therapeutic effect in psoriasis and pityriasis rosea, but on the other hand is aggravating for photodermatoses such as drug-induced photosensitivity, lupus and polymorphic eruption. Our studies suggest a less marked worsening of psoriasis in summer.

With the heat, there is increased activity of insects and poisonous animals and a higher exposure to outdoor activities, such as fishing and walks, what could explain the frequency of zoonoses at this time of the year.6,7

Some authors identified higher incidences of staphylococcal infections in the hotter and more humid months, explaining lower admission rates for bacterial infections in winter, which is dry and cold in the region.8 In the same way, the winter climate favors respiratory infections, which are associated to immune imbalances that can trigger leprosy reactions.9,10 Urticaria and rhinitis are associated to airborne allergens, more widespread in spring.

Besides drawing attention to an epidemiological alert for the control and prevention of damage, this study values the hospital integration of the dermatologist and directs the need for ongoing updates on these conditions, particularly with the progressive aging of the population.

This study presents limitations related to the accuracy of clinical records, limitations of the sensitivity of the method for identification of patterns in rare diseases and limitations since a large fraction of the diagnoses identified are treated in an outpatient setting.

The generalization of the results is impaired by the reality of the sample population: public service in a subtropical region. However, the discrepancies observed indicate biological or exposure elements that can be observed in patients from other regions or subject to travelling. Similar studies in different geopolitical conditions should investigate the seasonality of dermatological admissions according to each context.

Development and urbanization promote, besides increased life expectancy, an epidemiological transition altering the prevalences of diseases; however, that should not significantly interfere in their seasonality.

Many skin conditions that require hospital admission have seasonal patterns that should be taken into consideration for sizing the service and for primary prevention in the population.

Financial support: None.

Conflict of interest: None.

References
[1.]
C.S. Munro, J.G. Lowe, P. McLoone, M.I. White, JA. Hunter.
The value of in-patient dermatology: a survey of in-patients in Scotland and Northern England..
Br J Dermatol., 140 (1999), pp. 474-479
[2.]
L. de Paula Samorano-Lima, LM. Quitério, J.A. Sanches Jr, CF. Neto.
Inpatient dermatology: profile of patients and characteristics of admissions to a tertiary dermatology inpatient unit in Sao Paulo, Brazil..
Int J Dermatol., 53 (2014), pp. 685-691
[3.]
S. Banerjee, D.N. Gangopadhyay, S. Jana, M. Chanda.
Seasonal variation in pediatric dermatoses..
Indian J Dermatol., 55 (2010), pp. 44-46
[4.]
E. Bauer, C. Jahnke, H. Feldmeier.
Seasonal fluctuations of head lice infestation in Germany..
Parasitol Res., 104 (2009), pp. 677-681
[5.]
JJd. Souza Filho, RM Amorim Filho, F. Duarte, HA. Miot.
Pityriasis rosea: a review..
An Bras Dermatol., 73 (1998), pp. 245-250
[6.]
E.L. Gutierrez, C. Galarza, W. Ramos, M. Mendoza, M.E. Smith, A.G. Ortega-Loayza.
Influence of climatic factors on the medical attentions of dermatologic diseases in a hospital of Lima, Peru..
An Bras Dermatol., 85 (2010), pp. 461-468
[7.]
RS. Vetter.
Seasonality of brown recluse spiders, Loxosceles reclusa submitted by the general public: implications for physicians regarding loxoscelism diagnoses..
Toxicon., 58 (2011), pp. 623-625
[8.]
X. Wang, S. Towers, S. Panchanathan, G. Chowell.
A population based study of seasonality of skin and soft tissue infections: implications for the spread of CA-MRSA..
[9.]
S. Leekha, D.J. Diekema, EN. Perencevich.
Seasonality of staphylococcal infections..
Clin Microbiol Infect., 18 (2012), pp. 927-933
[10.]
P.R. Andrade, R.O. Pinheiro, A.M. Sales, X. Illarramendi, M.G. Barbosa, M.O. Moraes.
Type 1 reaction in leprosy: a model for a better understanding of tissue immunity under an immunopathological condition..
Expert Rev Clin Immunol., 11 (2015), pp. 391-407

Work conducted at the Department of Dermatology and Radiotherapy, Faculdade de Medicina de Botucatu, Universidade Estadual Paulista, Botucatu (SP), Brazil.

Copyright © 2018. Anais Brasileiros de Dermatologia
Baixar PDF
Idiomas
Anais Brasileiros de Dermatologia (Portuguese)
Opções de artigo
Ferramentas
en pt
Cookies policy Política de cookies
To improve our services and products, we use "cookies" (own or third parties authorized) to show advertising related to client preferences through the analyses of navigation customer behavior. Continuing navigation will be considered as acceptance of this use. You can change the settings or obtain more information by clicking here. Utilizamos cookies próprios e de terceiros para melhorar nossos serviços e mostrar publicidade relacionada às suas preferências, analisando seus hábitos de navegação. Se continuar a navegar, consideramos que aceita o seu uso. Você pode alterar a configuração ou obter mais informações aqui.