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1.
Ann Emerg Med ; 84(1): 40-48, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38493375

ABSTRACT

STUDY OBJECTIVE: In the early months of the coronavirus disease 2019 (COVID-19) pandemic and before vaccine availability, there were concerns that infected emergency department (ED) health care personnel could present a threat to the delivery of emergency medical care. We examined how the pandemic affected staffing levels and whether COVID-19 positive staff were potentially infectious at work in a cohort of US ED health care personnel in 2020. METHODS: The COVID-19 Evaluation of Risks in Emergency Departments (Project COVERED) project was a multicenter prospective cohort study of US ED health care personnel conducted from May to December 2020. During surveillance, health care personnel completed weekly electronic surveys and underwent periodic serology and nasal reverse transcription polymerase chain reaction testing for SARS-CoV-2, and investigators captured weekly data on health care facility COVID-19 prevalence and health care personnel staffing. Surveys asked about symptoms, potential exposures, work attendance, personal protective equipment use, and behaviors. RESULTS: We enrolled 1,673 health care personnel who completed 29,825 person weeks of surveillance. Eighty-nine (5.3%) health care personnel documented 90 (0.3%; 95% confidence interval [CI] 0.2% to 0.4%) person weeks of missed work related to documented or concerns for COVID-19 infection. Health care personnel experienced symptoms of COVID-19 during 1,256 (4.2%) person weeks and worked at least one shift whereas symptomatic during 1,042 (83.0%) of these periods. Seventy-five (4.5%) participants tested positive for SARS-CoV-2 during the surveillance period, including 43 (57.3%) who indicated they never experienced symptoms; 74 (98.7%; 95% CI 90.7% to 99.9%) infected health care personnel worked at least one shift during the initial period of infection, and 71 (94.7%) continued working until laboratory confirmation of their infection. Physician staffing was not associated with the facility or community COVID-19 levels within any time frame studied (Kendall tau's 0.02, 0.056, and 0.081 for no shift, one-week time shift, and 2-week time shift, respectively). CONCLUSIONS: During the first wave of the pandemic, COVID-19 infections in ED health care personnel were infrequent, and the time lost from the workforce was minimal. Health care personnel frequently reported for work while infected with SARS-CoV-2 before laboratory confirmation. The ED staffing levels were poorly correlated with facility and community COVID-19 burden.


Subject(s)
COVID-19 , Emergency Service, Hospital , Health Personnel , SARS-CoV-2 , Humans , COVID-19/epidemiology , United States/epidemiology , Prospective Studies , Emergency Service, Hospital/statistics & numerical data , Female , Male , Adult , Health Personnel/statistics & numerical data , Middle Aged , Personal Protective Equipment/supply & distribution , Personal Protective Equipment/statistics & numerical data , Pandemics , Infectious Disease Transmission, Patient-to-Professional/prevention & control
3.
Exp Dermatol ; 22(3): 236-8, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23489431

ABSTRACT

Traditional skin grafting techniques are effective but limited methods of skin replacement. Autologous transplantation of rapidly cultured keratinocytes is successful for epidermal regeneration, but the current gold-standard technique requires mouse fibroblast feeders and serum-rich media, with serum-free systems and dermal fibroblast (DF) feeders performing relatively poorly. Here, we investigated the capacity of human hair follicle dermal cells to act as alternative supports for keratinocyte growth. Dermal papilla (DP) dermal sheath (DS), DF and 3T3 cells were used as inactivated feeder cells for human keratinocyte coculture. Under conditions favouring dermal cells, proliferation of keratinocytes in the presence of either DS or DP cells was significantly enhanced compared with DF cells, at levels comparable to keratinocytes cultured under gold-standard conditions. Secreted protein acidic and rich in cysteine (SPARC) expression increased DS and DP cells relative to DFs; however, further experiments did not demonstrate a role in keratinocyte support.


Subject(s)
Cell Communication/physiology , Cell Proliferation , Dermis/cytology , Hair Follicle/cytology , Keratinocytes/cytology , 3T3 Cells/cytology , Animals , Coculture Techniques , Dermis/metabolism , Fibroblasts/cytology , Fibronectins/metabolism , Hair Follicle/metabolism , Humans , Keratinocytes/metabolism , Laminin/metabolism , Mice , Osteonectin , Skin Transplantation/physiology , Tumor Suppressor Proteins/metabolism
4.
Arch Dermatol ; 143(10): 1267-71, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17938340

ABSTRACT

OBJECTIVES: To prospectively determine the wound complication rate for dermatology inpatients undergoing diagnostic skin biopsies during their admission and to determine significant host and procedural risk factors. DESIGN: Prospective assessment, by a single observer, of 100 postdiagnostic skin biopsy wounds in dermatology inpatients. The following data were recorded for each patient: age and sex, presence of comorbidities, smoking status, dermatologic diagnosis, use of immunosuppressive or antibiotic therapy, place of biopsy (whether in the operation theater or in the ward), grade of physician performing biopsy, biopsy site on the body, type of biopsy (whether elliptical incision, punch, shave, or curettage), and wound closure technique. MAIN OUTCOME MEASURE: Wounds were designated as having had no complication or as being complicated by infection, dehiscence, and/or hematoma. SETTING: A dedicated dermatology inpatient ward in a university teaching hospital. RESULTS: Wound complications occurred in 29 (29%) biopsies, 27 (93%) of which were the result of wound infection. Complications occurred significantly more frequently when biopsies were performed below the waist compared with above the waist (P < .02), in the ward compared with the outpatient operating theater (P < .001), in smokers compared with nonsmokers (P < .001), and in those taking corticosteroids compared with those who were not (P < .001). In addition, elliptical incisional biopsies developed complications more frequently when subcutaneous sutures were not used compared with when they had been used (P < .001). CONCLUSIONS: This study has demonstrated a high rate of wound complications after diagnostic dermatologic surgery on dermatology inpatients with significant host and procedural risk factors. These findings are relevant for other centers with inpatient units where diagnostic biopsies are performed.


Subject(s)
Biopsy/adverse effects , Inpatients , Skin/pathology , Adrenal Cortex Hormones/adverse effects , Adrenal Cortex Hormones/therapeutic use , Adult , Aged , Aged, 80 and over , Biopsy/methods , Female , Humans , Incidence , Male , Methicillin Resistance , Middle Aged , Operating Rooms , Patients' Rooms , Postoperative Complications/epidemiology , Prospective Studies , Risk Factors , Smoking , Staphylococcal Skin Infections/epidemiology , Staphylococcal Skin Infections/physiopathology , Surgical Wound Dehiscence/epidemiology , Surgical Wound Infection/complications , Surgical Wound Infection/epidemiology
5.
J Travel Med ; 24(suppl_1): S35-S38, 2017 Apr 01.
Article in English | MEDLINE | ID: mdl-28520993

ABSTRACT

BACKGROUND: Antibiotics have profound and lasting effects on the lower intestinal (gut) microbiome that can both promote resistance and increase susceptibility to colonization and infection; knowledge of these changes is important to the prevention and treatment of traveler's diarrhea. METHODS: Recent data from epidemiologic and modern metagenomics studies were reviewed in regard to how such findings could inform the prevention and treatment of traveler's diarrhea. RESULTS: Although it is well recognized that antibiotics increase the risk for Clostridium difficile infection, it is less recognized how they predispose patients to typically foodborne pathogens such as Salmonella or Camplyobacter spp. While these pathogens account for only a fraction of traveler's diarrhea, such predisposition reflects how antibiotic exposure that precedes or occurs during travel may increase the risk for infection with other more common pathogens, even possibly enterotoxigenic Eschericia coli, especially in the setting of acquired resistance. Even short antibiotic exposures disrupt the gut microbiome up to a year or more and repeated exposures appear to attenuate recovery from ever occurring. One bacterial phylum that commonly increases in the gut following antibiotics are the proteobacteria including Enterobacteriacea; these are pro-inflammatory and often carry antibiotic resistance genes, the number and diversity of these genes (i.e. the resistome) commonly expands following antibiotics. The gut resistome among healthy community-dwelling adults reflects geographic variability in antibiotic use practices in both humans and food-producing animals as well as possibly the transmission of antibiotic resistance genes through the food supply. CONCLUSIONS: Because antibiotic use among travelers will influence the resistome and thereby promote geographic spread of resistance, it is important that antibiotic use recommendations for travelers be guided by resistance surveillance data as well as a careful assessment of the risks and benefits to both the individual and society.


Subject(s)
Anti-Bacterial Agents/pharmacology , Diarrhea/drug therapy , Gastrointestinal Microbiome/drug effects , Travel , Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents/therapeutic use , Humans
7.
Arch Dermatol ; 141(12): 1560-4, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16365258

ABSTRACT

BACKGROUND: Digital myxoid cysts (DMCs) are ganglia of the adjacent distal interphalangeal joint (DIPJ) caused by leakage of fluid from the joint into the surrounding tissues. The connection between the DIPJ and the cyst can be identified by the injection of methylene blue into the DIPJ. However, the injection of methylene blue into the DIPJ is difficult and time-consuming. Based on this understanding of the cause of DMCs, we have used a surgical technique to treat DMCs without the need for skin excision. Herein, we have adapted the technique and demonstrated that precise leakage point identification is not required for treatment success, thus reducing the potential postoperative morbidity, reducing the operative time, and simplifying the surgical technique. DESIGN: This was a prospective, open, nonrandomized trial of therapy. A skin flap was designed to include the cyst and tissues from the cyst to the DIPJ. No skin excision was required, and no osteophyte removal was attempted. SETTING: University dermatology department. PATIENTS: Thirty-two consecutive symptomatic subjects with 26 finger DMCs and 6 toe DMCs. No patient had been previously treated. MAIN OUTCOME MEASURES: Clinical assessment postoperatively and recurrence rate after a minimum follow-up of 8 months. RESULTS: Of the 26 finger DMCs, 24 (92.3%) remained healed at 8 months; and of the 6 toe DMCs, 2 (33.3%) remained healed at 8 months. CONCLUSIONS: Digital myxoid cysts are caused by leakage of joint fluid from the DIPJ to the cyst. The leakage point is sealed in the healing process that occurs after a flap is raised and re-sited. The flap must be designed to include the undersurface of the cyst and the tissues between the DIPJ and the cyst. No skin excision or osteophyte removal is required. The procedure is not recommended for DMCs of the toes.


Subject(s)
Dermatologic Surgical Procedures , Finger Joint/surgery , Joint Loose Bodies/surgery , Surgical Flaps , Synovial Cyst/surgery , Toe Joint/surgery , Adult , Aged , Female , Finger Joint/pathology , Humans , Male , Middle Aged , Prospective Studies , Skin/pathology , Synovial Cyst/pathology , Toe Joint/pathology , Treatment Outcome
8.
Arch Dermatol ; 140(1): 83-8, 2004 Jan.
Article in English | MEDLINE | ID: mdl-14732664

ABSTRACT

BACKGROUND: Review of the literature reveals that congenital malignant melanoma is an exceptionally rare occurrence and has a generally poor prognosis when it does occur. However, benign proliferative melanocytic lesions are known to occur within giant congenital nevi (GCN). This entity is not well recognized and can be confused clinically and histologically with malignant change. OBSERVATIONS: We report 2 cases of GCN in neonates demonstrating benign proliferating nodules present at birth. An initial diagnosis of malignant melanoma was assumed in both cases. Careful histologic analysis, however, revealed these lesions to be benign, as did long-term follow-up of 3.5 years, with both patients remaining well with no evidence of melanoma. Review of the literature suggests that there are 2 clinical patterns of these benign nodules arising within GCNs: small (<1 cm) and large (>1 cm) dermal nodules with varying histologic patterns that we have attempted to categorize. CONCLUSIONS: Our cases illustrate the difficulty in accurate diagnosis of melanocytic lesions in the neonate. We recommend caution in making a diagnosis of malignant melanoma and highlight the possibility that benign lesions can be mistaken for melanoma in this age group. We encourage the acquisition of fixed histologic specimens for accurate diagnosis of melanocytic lesions.


Subject(s)
Nevus, Pigmented/congenital , Skin Neoplasms/congenital , Diagnosis, Differential , Female , Humans , Infant, Newborn , Melanoma/congenital , Melanoma/diagnosis , Nevus, Pigmented/diagnosis , Nevus, Pigmented/pathology , Skin Neoplasms/diagnosis , Skin Neoplasms/pathology
9.
Clin Med (Lond) ; 3(5): 440-2, 2003.
Article in English | MEDLINE | ID: mdl-14601943

ABSTRACT

The NHS plan promises the creation of general practitioners with a specialist interest (GPSIs) who will be able to provide an alternative referral resource for primary care. At present, only the specialties of orthopaedics, ophthalmology, ENT and dermatology, which have the longest waiting times for outpatient appointments, have been earmarked for GPSIs. The British Association of Dermatologists has examined, investigated and piloted several such schemes for dermatology provision. This paper summarises its principal conclusions.


Subject(s)
Attitude of Health Personnel , Dermatology , Interprofessional Relations , Physicians, Family/organization & administration , Delivery of Health Care/organization & administration , Humans , National Health Programs , United Kingdom , Workload
10.
PLoS One ; 7(11): e50742, 2012.
Article in English | MEDLINE | ID: mdl-23226372

ABSTRACT

Human multipotent skin derived precursor cells (SKPs) are traditionally sourced from dissociated dermal tissues; therefore, donor availability may become limiting. Here we demonstrate that both normal and diseased adult human dermal fibroblasts (DF) pre-cultured in conventional monolayers are capable of forming SKPs (termed m-SKPs). Moreover, we show that these m-SKPs can be passaged and that cryopreservation of original fibroblast monolayer cultures does not reduce m-SKP yield; however, extensive monolayer passaging does. Like SKPs generated from dissociated dermis, these m-SKPs expressed nestin, fibronectin and versican at the protein level. At the transcriptional level, m-SKPs derived from normal adult human DF, expressed neural crest stem cell markers such as p75NTR, embryonic stem cell markers such as Nanog and the mesenchymal stem cell marker Dermo-1. Furthermore, appropriate stimuli induced m-SKPs to differentiate down either mesenchymal or neural lineages resulting in lipid accumulation, calcification and S100ß or ß-III tubulin expression (with multiple processes). m-SKP yield was greater from neonatal foreskin cultures compared to those from adult DF cultures; however, the former showed a greater decrease in m-SKP forming capacity after extensive monolayer passaging. m-SKP yield was greater from adult DF cultures expressing more alpha-smooth muscle actin (αSMA). In turn, elevated αSMA expression correlated with cells originating from specimens isolated from biopsies containing more terminal hair follicles; however, αSMA expression was lost upon m-SKP formation. Others have shown that dissociated human hair follicle dermal papilla (DP) are a highly enriched source of SKPs. However, conversely and unexpectedly, monolayer cultured human hair follicle DP cells failed to form m-SKPs whereas those from the murine vibrissae follicles did. Collectively, these findings reveal the potential for using expanded DF cultures to produce SKPs, the heterogeneity of SKP forming potential of skin from distinct anatomical locations and ages, and question the progenitor status of human hair follicle DP cells.


Subject(s)
Dermis/cytology , Multipotent Stem Cells/cytology , Actins/metabolism , Adipogenesis , Adult , Biomarkers/metabolism , Cells, Cultured , Cryopreservation , Dermis/pathology , Female , Fibroblasts/cytology , Fibroblasts/pathology , Humans , Intermediate Filament Proteins/metabolism , Male , Middle Aged , Multipotent Stem Cells/metabolism , Nerve Tissue Proteins/metabolism , Nestin , Neurons/cytology , Osteogenesis , Schwann Cells/cytology , Up-Regulation , Versicans/metabolism
13.
J Investig Dermatol Symp Proc ; 10(3): 180-3, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16382659

ABSTRACT

The dermal components of the hair follicle exhibit a number of stem cell properties, including regenerative potential, roles in wound healing and the ability to produce a functional dermis. Here we examine the stem cell phenomenon of plasticity, focusing on recent observations of in vitro plasticity of dermal papilla and sheath cells, including previously unpublished data of neuronal-like differentiation. We then briefly address the implications of the stem cell potential of hair follicle dermal cells for the field of tissue engineering.


Subject(s)
Cell Differentiation/physiology , Dermis/physiology , Hair Follicle/physiology , Animals , Cell- and Tissue-Based Therapy , Dermis/cytology , Hair Follicle/cytology , Humans , Rats , Stem Cells/physiology , Tissue Engineering
15.
J Clin Microbiol ; 40(4): 1526-9, 2002 Apr.
Article in English | MEDLINE | ID: mdl-11923388

ABSTRACT

We determined the clinical and microbiologic characteristics of community-acquired Acinetobacter baumannii bacteremia in 19 adult patients. We found that malignancy was the most frequent underlying disease. The overall mortality rate was 58%. All 14 available isolates were identified as genomic species 2 (A. baumannii) by 16S ribosomal DNA sequencing and were found to be genetically distinct by pulsed-field gel electrophoresis.


Subject(s)
Acinetobacter Infections/microbiology , Acinetobacter/classification , Acinetobacter/isolation & purification , Bacteremia/microbiology , Community-Acquired Infections/microbiology , Acinetobacter/genetics , Acinetobacter Infections/mortality , Adult , Aged , Aged, 80 and over , Bacteremia/mortality , Community-Acquired Infections/mortality , Electrophoresis, Gel, Pulsed-Field , Female , Humans , Male , Middle Aged , Taiwan
16.
Rio de Janeiro; Revinter; 1997. 90 p. ilus.
Monography in Portuguese | SMS-SP, AHM-Acervo, TATUAPE-Acervo | ID: sms-7166
17.
London; Mosby-Wolfe; 1998. v,186 p. ilus, tab, 29cm.
Monography in English | LILACS, HANSEN, Hanseníase (leprosy), SESSP-ILSLACERVO, SES-SP | ID: biblio-1086365
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