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1.
Pediatrics ; 145(4)2020 04.
Artigo em Inglês | MEDLINE | ID: mdl-32161112

RESUMO

OBJECTIVES: Infantile hemangiomas (IHs) are common; some cases require timely referral and treatment to prevent complications. We developed and validated a reliable instrument for timely and adequate referral of patients with IH to experts by nonexpert primary physicians. METHODS: In this multicenter, cross-sectional, observational study, we used a 3-stage process: (1) development of the Infantile Hemangioma Referral Score (IHReS) tool by IH experts who selected a representative set of 42 IH cases comprising images and a short clinical history, (2) definition of the gold standard for the 42 cases by a second independent committee of IH experts, and (3) IHReS validation by nonexpert primary physicians using the 42 gold standard cases. RESULTS: A total of 60 primary physicians from 7 different countries evaluated the 42 gold standard cases (without reference to the IHReS tool); 45 primary physicians evaluated these cases using the IHReS questionnaire, and 44 completed retesting using the instrument. IHReS had a sensitivity of 96.9% (95% confidence interval 96.1%-97.8%) and a specificity of 55.0% (95% confidence interval 51.0%-59.0%). The positive predictive value and negative predictive value were 40.5% and 98.3%, respectively. Validation by experts and primary physicians revealed substantial agreement for interrater reliability and intrarater repeatability. CONCLUSIONS: IHReS, a 2-part algorithm with a total of 12 questions, is an easy-to-use tool for primary physicians for the purpose of facilitating correct and timely referral of patients with IH. IHReS may help practitioners in their decision to refer patients to expert centers.


Assuntos
Comitês Consultivos/normas , Algoritmos , Hemangioma/terapia , Encaminhamento e Consulta/normas , Intervalos de Confiança , Estudos Transversais , Hemangioma/classificação , Hemangioma/patologia , Humanos , Lactente , Variações Dependentes do Observador , Curva ROC , Reprodutibilidade dos Testes , Sensibilidade e Especificidade , Inquéritos e Questionários
2.
Pediatr Dermatol ; 36(6): 958-960, 2019 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-31566792

RESUMO

This study compares the quality of life (QoL) of infantile hemangioma (IH) patients and their parents at the beginning of the involution phase with QoL in the growth phase. Additionally, the differences in QoL between propranolol-treated patients and non-treated patients are assessed. Overall, QoL seems to improve, even before involution occurs. Due to the efficacy of propranolol treatment, the impact on QoL remains relatively mild even in patients with severe IH.


Assuntos
Hemangioma/tratamento farmacológico , Pais/psicologia , Propranolol/uso terapêutico , Qualidade de Vida , Neoplasias Cutâneas/tratamento farmacológico , Pré-Escolar , Estudos de Coortes , Feminino , Seguimentos , Humanos , Lactente , Masculino , Índice de Gravidade de Doença , Vasodilatadores/uso terapêutico
3.
Skin Res Technol ; 25(5): 618-624, 2019 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-30942508

RESUMO

BACKGROUND: Vascular changes, that is, functional and cellular endothelial changes, are of essential importance in healing. Alongside these vascular changes, inflammatory factors and hypoxia may play an important role in recovery. OBJECTIVES: To investigate the dynamics of functional and cellular endothelial changes and hypoxia in vivo following standardized skin damage caused by tape stripping. METHODS: Vascular changes (endothelial cell proliferation, vascular network size, vessel diameter) and hypoxia-inducible factor-1α were examined immunohistochemically using a CD31/Ki67 double staining and HIF-1α single staining. Cutaneous perfusion was evaluated using the Twente Optical Perfusion Camera (TOPCam). RESULTS: The initial phase is seen to be dominated by endothelial cell proliferation, HIF-1α expression, and vasodilatation. Cutaneous perfusion intensity is particularly increased in the first 16 hours. The late phase of recovery (after 72 hours) is characterized by a peak of expansion of the vascular network and a second peak of endothelial cell proliferation and HIF-1α expression. CONCLUSION: Endothelial cell proliferation and HIF-1α expression appear to be (strongly) related, having maximum levels at 16 hours and 72 hours. Angiogenesis and HIF-1α expression are not continuous processes, but rather occur intermittently.


Assuntos
Eritema/patologia , Pele/lesões , Adolescente , Adulto , Biomarcadores/metabolismo , Biópsia , Vasos Sanguíneos/fisiologia , Hipóxia Celular/fisiologia , Proliferação de Células/fisiologia , Células Endoteliais/citologia , Endotélio Vascular/citologia , Feminino , Voluntários Saudáveis , Humanos , Subunidade alfa do Fator 1 Induzível por Hipóxia/metabolismo , Imuno-Histoquímica , Antígeno Ki-67/metabolismo , Masculino , Pessoa de Meia-Idade , Fotografação , Pele/irrigação sanguínea , Pele/citologia , Adulto Jovem
4.
Pediatr Dermatol ; 35(5): 628-634, 2018 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-30015356

RESUMO

BACKGROUND: Quality of life (QoL) data are lacking in children with infantile hemangioma (IH) and their parents/caregivers. Available data are conflicting. OBJECTIVES: To determine QoL of (parents of) patients with IH in the proliferative phase related to IH-severity and activity. METHODS: Parents of 59 IH-patients (≤ 6 months) were asked to fill in the Dutch IH-specific QoL-questionnaire (D-IH-QoL) within 1 month after their first visit to our tertiary referral center. Hemangioma Severity Scale (HSS) score and Hemangioma Activity Score (HAS) were assessed. RESULTS: D-IH-QoL-scores were low; mean: 22.6 (range 1-56; max 116). Mean HSS score and HAS score were 8.4 (range 2-28) and 4.0 (range 1.5-6), respectively. Higher HSS scores correlated with worse QoL (ρ = .358; P = .005). HAS scores did not correlate with QoL scores. CONCLUSION: An IH only seems to have limited influence on QoL in young children and their parents in the first month of their first doctor's visit. QoL is more affected in more severe IH. Physicians should be alert to the impact of IH, optionally guided by the HSS score.


Assuntos
Hemangioma/psicologia , Pais/psicologia , Pacientes/psicologia , Qualidade de Vida/psicologia , Neoplasias Cutâneas/psicologia , Cuidadores/psicologia , Estudos Transversais , Feminino , Humanos , Lactente , Masculino , Índice de Gravidade de Doença , Inquéritos e Questionários
5.
J Am Acad Dermatol ; 77(5): 868-873, 2017 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-28818436

RESUMO

BACKGROUND: The Hemangioma Severity Scale (HSS) assesses the severity of an infantile hemangioma (IH). OBJECTIVE: First, to compare HSS scores between patients with IH for whom propranolol treatment was indicated at their first visit and those who were not treated. Second, to assess suitable cutoff values for the need for propranolol treatment. METHOD: All patients with IH who attended our tertiary referral center since 2008 and were 0 to 6 months of age at their first visit were included. They were divided into propranolol and no-propranolol groups on the basis of choice of treatment at their first visit. HSS scores were assessed, and median scores were compared. RESULTS: A total of 657 children (342 in the propranolol group) were included. The median HSS score (25th-75th percentile) in the propranolol group was 10 (range, 8-14) compared with 7 (range, 4-9) in the no-propranolol group (P < .001). Cutoff values of 6 or lower (no indication for treatment) and 11 or higher (indication for treatment) resulted in 94% sensitivity and 89% specificity, respectively. LIMITATIONS: HSS scoring was not completely blinded. CONCLUSION: The HSS with cutoff values of 6 or lower and 11 or higher could be used as a triage tool for propranolol treatment. Patient age, IH type, and parental preference may also contribute to treatment decisions.


Assuntos
Tomada de Decisão Clínica , Hemangioma Capilar/tratamento farmacológico , Hemangioma Capilar/patologia , Propranolol/uso terapêutico , Índice de Gravidade de Doença , Neoplasias Cutâneas/tratamento farmacológico , Estudos de Coortes , Bases de Dados Factuais , Feminino , Seguimentos , Hemangioma/tratamento farmacológico , Hemangioma/epidemiologia , Hemangioma/patologia , Hemangioma Capilar/epidemiologia , Humanos , Lactente , Recém-Nascido , Masculino , Seleção de Pacientes , Valores de Referência , Estudos Retrospectivos , Medição de Risco , Neoplasias Cutâneas/epidemiologia , Neoplasias Cutâneas/patologia , Estatísticas não Paramétricas , Centros de Atenção Terciária , Resultado do Tratamento
6.
J Am Acad Dermatol ; 77(1): 105-108, 2017 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-28190620

RESUMO

BACKGROUND: Concern has been raised about the potential long-term effects of propranolol treatment for infantile hemangioma (IH). OBJECTIVES: We sought to assess psychologic (social, emotional, behavioral, and executive) functioning in children treated with propranolol for IH. METHODS: Twenty-seven patients with IH (6.1-7.6 years of age) treated with propranolol for ≥6 months during infancy, and without other developmental risk factors, were recruited. Parents completed the Behavior Rating Inventory of Executive Function, Social Emotional Questionnaire, Child Behavior Checklist, and Strengths and Difficulties Questionnaire. For each questionnaire, the number of patients with abnormal scores, based on established cutoff points, was calculated. RESULTS: Only 1 child (3.7%) scored outside the normal range. The Hemangioma Severity Scale did not correlate with psychologic problems in these patients. Longer treatment duration was found to correlate with less attention-deficit hyperactivity disorder (ADHD) characteristics (ρ = -0.476; P = .012) and better executive functioning (ρ = -0.466; P = .014). LIMITATIONS: Exclusion of children born at gestational age <36 weeks or small for gestational age, no reference group and relatively small study size. CONCLUSION: We found no increased risk for psychologic problems at age 7 in IH patients treated with propranolol.


Assuntos
Hemangioma/tratamento farmacológico , Transtornos Mentais/induzido quimicamente , Propranolol/efeitos adversos , Neoplasias Cutâneas/tratamento farmacológico , Criança , Feminino , Humanos , Masculino , Propranolol/uso terapêutico , Estudos Prospectivos , Testes Psicológicos
7.
J Am Acad Dermatol ; 75(1): 59-63.e1, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27021240

RESUMO

BACKGROUND: Long-term adverse effects of propranolol treatment for infantile hemangioma (IH) in young children have been suggested. OBJECTIVE: To compare growth and development in children treated with propranolol for IH with nontreated healthy controls. METHODS: Eighty two (73%) children with IH aged 43 to 51 months treated with propranolol for 6 months or longer, and without other developmental risk factors, were recruited (cases) and matched with 4 twin counterparts and 78 children from a community-based cohort (control subjects). Parents completed the 48-months Ages and Stages Questionnaire (ASQ). Percentages of children with abnormal ASQ results were compared using χ(2) analyses. Mean ASQ scores and growth were compared using Mann-Whitney U tests. RESULTS: Six (7.3%) cases had abnormal ASQ results, compared with 10 (12.2%) controls (P = .292). Mean ASQ total score (25th-75th percentile) was 52.9 (50.8-57.0) for cases and 51.9 (49.0-56.0) for controls (P = .383). Height and weight of cases and controls were comparable. LIMITATIONS: A parent-completed screening instrument was used. The exclusion of children born at gestational age less than 36 weeks and/or children born small for gestational age partly limits generalizability. CONCLUSION: We found no increased developmental risk or growth impairment at age 4 years in patients with IH treated with propranolol.


Assuntos
Desenvolvimento Infantil/efeitos dos fármacos , Hemangioma Capilar/tratamento farmacológico , Síndromes Neoplásicas Hereditárias/tratamento farmacológico , Propranolol/efeitos adversos , Vasodilatadores/efeitos adversos , Estatura , Peso Corporal , Estudos de Casos e Controles , Pré-Escolar , Feminino , Humanos , Lactente , Recém-Nascido , Masculino , Transtornos do Humor/induzido quimicamente , Propranolol/uso terapêutico , Transtornos do Sono-Vigília/induzido quimicamente , Inquéritos e Questionários , Fatores de Tempo , Vasodilatadores/uso terapêutico
9.
Pediatr Dermatol ; 31(1): 118-22, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24106998

RESUMO

Accurate and objective measurement of volume changes in infantile hemangiomas (IHs) is essential in routine clinical practice and clinical studies, particularly in the changing therapeutic landscape after the discovery of propranolol. Several bedside techniques for volume measurement have been described in the literature, but an objective method of measurement of this variable, dynamic vascular tumor is lacking. Three-dimensional (3D) phototechnology with data analysis is an up-and-coming technique in the objective measurement of facial volume changes. In this pilot study, the usability and clinical relevance of two methods of 3D stereophotogrammetry in the volume measurement of IH were explored.


Assuntos
Hemangioma/diagnóstico , Imageamento Tridimensional/métodos , Fotogrametria/métodos , Neoplasias Cutâneas/diagnóstico , Superfície Corporal , Face/patologia , Feminino , Hemangioma/patologia , Humanos , Lactente , Masculino , Projetos Piloto , Estudos Prospectivos , Neoplasias Cutâneas/patologia
10.
Eur J Dermatol ; 23(6): 857-63, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24185746

RESUMO

BACKGROUND: Infantile hemangiomas (IHs) are common and mostly emerge in the head-neck area. Recently, propranolol has been replacing oral corticosteroids (OCS) as the main treatment modality. OBJECTIVES: The aim of this study was to explore the impact of treatment, contentment with treatment outcome and quality of life for families and patients with cervicofacial IHs, treated with propranolol versus OCS. MATERIALS AND METHODS: This study was performed using questionnaires administered by a phone interview. Parents of 16 patients with a cervicofacial IH treated by OCS and 16 patients with an IH of similar localization and overall severity treated with propranolol were interviewed. The questions concerned the impact of treatment at different time periods and the contentment with treatment results. Parents were also asked to give a quality of life (QoL) score (1 to 10) for different time-points. RESULTS: Parents from the OCS group seemed to feel significantly more worried during treatment. Moreover, parents from the propranolol group perceived less negative impact on normal life issues, including work and vaccination of their child. During and after treatment, the parents of propranolol-treated IH patients gave significantly higher QoL scores. CONCLUSION: Propranolol seems to change the impact of IHs, their treatment and the quality of life. Propranolol treatment interferes less with normal issues in daily life, compared to OCS. These findings underline propranolol as the first choice treatment for life- or function-threatening IHs.


Assuntos
Corticosteroides/uso terapêutico , Dermatoses Faciais/tratamento farmacológico , Hemangioma Capilar/tratamento farmacológico , Síndromes Neoplásicas Hereditárias/tratamento farmacológico , Pais/psicologia , Propranolol/uso terapêutico , Vasodilatadores/uso terapêutico , Corticosteroides/administração & dosagem , Adulto , Pré-Escolar , Dermatoses Faciais/congênito , Feminino , Humanos , Lactente , Masculino , Pescoço , Satisfação do Paciente , Qualidade de Vida/psicologia , Estudos Retrospectivos , Inquéritos e Questionários , Resultado do Tratamento
11.
Int J Pediatr Otorhinolaryngol ; 77(11): 1791-800, 2013 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-24074695

RESUMO

OBJECTIVES: Infantile hemangiomas (IHs) in the airway may be potentially life-threatening during the proliferative phase. Available treatments like oral corticosteroids (OCS) and chemotherapeutic agents usually showed variable responses and serious side effects. Propranolol is a new and promising treatment option. METHODS: A case series of five IH patients with airway involvement is presented, supplemented with a review of literature. Propranolol treatment (2.0-3.0mg/kg/day) was initiated between 3 weeks and 6 months of age. Three cases were treated with propranolol monotherapy, 2 cases with OCS primarily and propranolol secondarily, in which treatment with OCS could be reduced rapidly. RESULTS: In our case series a dramatic, fast response was observed in all cases, with a permanent effect after discontinuation in four cases. In one patient a relapse of airway problems occurred two months after discontinuation of propranolol at 16 months of age; this resolved after re-start of propranolol. Review of literature together with these five cases showed 81 patients with airway IHs treated with propranolol. Propranolol was effective in 90% of the cases and seven patients were classified as non-responders. Eight IHs relapsed while weaning of propranolol or after discontinuation; dose adjustment or restart was effective in most cases but one patient appeared resistant to therapy. CONCLUSIONS: Propranolol seems to be a rapidly effective and safe treatment strategy for most IHs obstructing the airway. Because of the fast and important effects of propranolol, randomized controlled trials are hardly justifiable for this specific, relatively rare but, acute treatment indication. Despite the efficacy of propranolol, close monitoring of the patients with an airway IH is required, considering the risk of relapse of symptoms during or after treatment and the reported resistance to propranolol in at least 9% of the published cases. The dose and duration of treatment should be high and long enough to prevent relapse. Further research should focus on the optimal treatment protocol; the actual percentage of non-responders and also the mechanism of resistance to propranolol is unknown and needs to be illuminated.


Assuntos
Obstrução das Vias Respiratórias/tratamento farmacológico , Obstrução das Vias Respiratórias/patologia , Hemangioma Capilar/tratamento farmacológico , Propranolol/administração & dosagem , Neoplasias Cutâneas/tratamento farmacológico , Administração Oral , Obstrução das Vias Respiratórias/etiologia , Biópsia por Agulha , Estado Terminal , Relação Dose-Resposta a Droga , Esquema de Medicação , Feminino , Seguimentos , Hemangioma Capilar/complicações , Hemangioma Capilar/congênito , Humanos , Imuno-Histoquímica , Lactente , Recém-Nascido , Masculino , Segurança do Paciente , Medição de Risco , Estudos de Amostragem , Neoplasias Cutâneas/complicações , Neoplasias Cutâneas/congênito , Resultado do Tratamento
12.
J Pediatr Hematol Oncol ; 33(4): e171-3, 2011 May.
Artigo em Inglês | MEDLINE | ID: mdl-21516018

RESUMO

Kaposiform hemangioendothelioma is a rare vascular tumor in children. Especially, in association with the Kasabach-Merritt Phenomenon it can be life threatening. The management of these patients is very difficult and an aggressive treatment regime is required. Several multimodality and chemotherapeutic regimens have been described but with variable success and many side effects. We present a 6-week-old boy with Kaposiform hemangioendothelioma and Kasabach-Merritt Phenomenon. Ongoing propranolol treatment with only 4 initial courses of vincristine resulted in a remission that lasted at least 1 year.


Assuntos
Antagonistas Adrenérgicos beta/administração & dosagem , Propranolol/administração & dosagem , Antineoplásicos Fitogênicos/administração & dosagem , Coagulação Intravascular Disseminada/tratamento farmacológico , Coagulação Intravascular Disseminada/etiologia , Quimioterapia Combinada , Hemangioendotelioma/complicações , Hemangioendotelioma/tratamento farmacológico , Hemangioma Capilar/tratamento farmacológico , Hemangioma Capilar/etiologia , Hemangioma Cavernoso/complicações , Hemangioma Cavernoso/tratamento farmacológico , Humanos , Lactente , Síndrome de Kasabach-Merritt , Masculino , Indução de Remissão , Sarcoma de Kaposi/complicações , Sarcoma de Kaposi/tratamento farmacológico , Neoplasias Cutâneas/complicações , Neoplasias Cutâneas/tratamento farmacológico , Trombocitopenia/complicações , Trombocitopenia/tratamento farmacológico , Neoplasias Vasculares/complicações , Neoplasias Vasculares/tratamento farmacológico , Vincristina/administração & dosagem
13.
J Am Acad Dermatol ; 64(5): 833-8, 2011 May.
Artigo em Inglês | MEDLINE | ID: mdl-21353329

RESUMO

BACKGROUND: Ulceration is a common but poorly understood complication of infantile hemangiomas (IH) that is difficult to control. OBJECTIVE: To investigate the possible role of monotherapy with propranolol for ulcerating IH. METHODS: Propranolol was given to 20 patients with IH, who suffered from ulceration at the start of treatment (mean age at onset of treatment, 3.5 months; standard error of the mean: 0.4). After cardiac screening, propranolol was administered in a progressive schedule to 2 to 2.5 mg/kg per day, divided in 3 doses. Blood pressure, heart rate, and fasting glucose levels were monitored during the first 3 days in hospital and, in the absence of complications, treatment was continued at home until the age of approximately 1 year. The 20 propranolol-treated patients were matched to patients from a historical control group, seen before the 'propranolol era'. These matches were randomly made by using clinical pictures based on type, location and size of the IH, extent of ulceration, and age at the start of ulceration. RESULTS: The time to complete healing from the onset of ulceration was significantly shorter for the propranolol-treated patients, compared with the control group (8.7 vs 22.4 weeks; t test: P < .015). In the propranolol group, a tendency to shorter ulceration duration was seen in patients starting propranolol at an earlier stage of disease. LIMITATIONS: The study was limited by the partially retrospective design and the small number of patients. CONCLUSION: Propranolol reduces the duration of ulceration in IH and seems to be more effective when started in an early phase. We propose propranolol as the treatment of first choice for ulcerating IH.


Assuntos
Antagonistas Adrenérgicos beta/uso terapêutico , Hemangioma/tratamento farmacológico , Hemangioma/patologia , Propranolol/uso terapêutico , Neoplasias Cutâneas/tratamento farmacológico , Antagonistas Adrenérgicos beta/administração & dosagem , Feminino , Neoplasias de Cabeça e Pescoço/tratamento farmacológico , Hemangioma/complicações , Humanos , Lactente , Masculino , Propranolol/administração & dosagem , Úlcera Cutânea/tratamento farmacológico , Úlcera Cutânea/etiologia , Resultado do Tratamento , Cicatrização/efeitos dos fármacos
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