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3.
Clin Radiol ; 72(3): 179-188, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28063602

RESUMO

Recognising the skeletal manifestations of inflicted injury (II) in infants and young children is of crucial importance. There are specific fracture patterns which are highly suspicious of II in addition to common differential diagnoses with which radiologists should be familiar. Our objective is to provide a non-exhaustive review of the important factors relevant to the imaging and reporting of II as a platform for further learning. Part 1 encompasses important initial considerations and fracture patterns of the appendicular skeleton.


Assuntos
Maus-Tratos Infantis/diagnóstico , Documentação/normas , Fraturas Ósseas/diagnóstico por imagem , Notificação de Abuso , Guias de Prática Clínica como Assunto , Radiografia/normas , Acidentes , Criança , Maus-Tratos Infantis/classificação , Pré-Escolar , Feminino , Fraturas Ósseas/classificação , Fidelidade a Diretrizes , Humanos , Lactente , Recém-Nascido , Masculino , Reino Unido
4.
Clin Radiol ; 72(3): 189-201, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28027778

RESUMO

Recognising the skeletal manifestations of inflicted injury (II) in infants and young children is of crucial importance. There are specific fracture patterns which are highly suspicious of II in addition to common differential diagnoses with which radiologists should be familiar. Our objective is to provide a non-exhaustive review of the important factors relevant to the imaging and reporting of II as a platform for further learning. Part 2 encompasses fracture patterns of the axial skeleton and important differential diagnoses.


Assuntos
Maus-Tratos Infantis/diagnóstico , Documentação/normas , Fraturas Ósseas/diagnóstico por imagem , Notificação de Abuso , Guias de Prática Clínica como Assunto , Radiografia/normas , Acidentes , Criança , Maus-Tratos Infantis/classificação , Pré-Escolar , Feminino , Fraturas Ósseas/classificação , Fidelidade a Diretrizes , Humanos , Lactente , Recém-Nascido , Masculino , Reino Unido
5.
Ann R Coll Surg Engl ; 93(5): 405-9, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-21943467

RESUMO

INTRODUCTION: Although regular clinical assessment of the acute abdomen is considered best practice, ultrasonography confirming the presence of appendicitis will add to the decision-making process. The aim of this study was to assess the accuracy of ultrasonography and its usefulness in diagnosing acute appendicitis in a regional paediatric surgical institution. METHODS: Retrospectively and in this order, radiology, theatre and histopathology databases were searched for patients who had presented with acute abdominal pain, patients who had undergone an appendicectomy and all appendix specimens over a two-year period. The databases were cross-referenced against each other. RESULTS: A total of 273 non-incidental appendicectomies were performed over the study period. The negative appendicectomy rate was 16.5% and the perforation rate 23.7%. Thirty-nine per cent of children undergoing an appendicectomy had at least one pre-operative ultrasound scan. Ultrasonography as a diagnostic tool for acute appendicitis in children had a sensitivity of 83.3%, a specificity of 97.4%, a positive predictive value of 92.1% and a negative predictive value of 94.0%. CONCLUSIONS: Ultrasonography is used liberally to aid in the decision making process of equivocal and complicated cases of acute appendicitis and it achieves good measures of accuracy. As a diagnostic tool it is unique in its ability to positively predict as well as exclude. A high negative predictive value suggests that more patients could be managed on an outpatient basis following a negative scan.


Assuntos
Dor Abdominal/diagnóstico por imagem , Apendicite/diagnóstico por imagem , Abdome Agudo/diagnóstico por imagem , Abdome Agudo/etiologia , Dor Abdominal/etiologia , Adolescente , Apendicectomia/estatística & dados numéricos , Criança , Pré-Escolar , Estudos Transversais , Diagnóstico Diferencial , Humanos , Lactente , Perfuração Intestinal/diagnóstico por imagem , Sensibilidade e Especificidade , Ultrassonografia
8.
Pediatr Surg Int ; 24(2): 241-3, 2008 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-17987304

RESUMO

Ano-rectal malformations (ARM) in the male patient may be associated with a fistulous communication between the rectum and urethra. Pre-operative radiological assessment is important to delineate (a) the presence and level of the fistula, (b) the anatomy of the posterior urethra and (c) any anomalies in adjacent structures. Bladder catheterisation can be technically difficult when performing an MCUG and distal loopogram in such patients. This can be due to urethral stricture, tortuous or kinked urethra or preferential passage of catheter into a large fistula and leads to an inadequate study. We describe a "double urethral catheter technique" to enable urethral catheterisation when the fistula is large.


Assuntos
Canal Anal/anormalidades , Fístula Retal/cirurgia , Reto/anormalidades , Uretra/anormalidades , Cateterismo Urinário/métodos , Fístula Urinária/cirurgia , Urografia/métodos , Humanos , Lactente , Masculino , Fístula Retal/diagnóstico por imagem , Fístula Urinária/diagnóstico por imagem , Micção
9.
Eur J Pediatr Surg ; 16(1): 55-7, 2006 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-16544229

RESUMO

We describe a case of subcapsular haematoma of the right lobe (SHL) and multifocal necrosis of the left lobe (MNL) of the liver following umbilical vein catheterisation (UVC) in a female at 24 weeks' gestation. SHL and MNL have been described as uncommon complications following umbilical vein catheterisation. To our knowledge this is the first time both complications have developed in the same patient. SHL should be considered in the differential diagnosis of hypovolaemic shock in this group of patients.


Assuntos
Cateterismo/efeitos adversos , Hematoma/etiologia , Recém-Nascido Prematuro , Hepatopatias/etiologia , Veias Umbilicais , Evolução Fatal , Feminino , Humanos , Recém-Nascido , Hepatopatias/patologia , Necrose
10.
BJOG ; 111(8): 784-92, 2004 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-15270925

RESUMO

OBJECTIVE: To compare the diagnostic accuracy of the current reference standard-ultrasound with in utero magnetic resonance imaging, in a selected group of patients. DESIGN: Prospective study. SETTING: Five fetal maternal tertiary referral centres and an academic radiology unit. SAMPLE: One hundred cases of fetuses with central nervous system abnormalities where there has been diagnostic difficulties on ultrasound. In 48 cases the women were less than 24 weeks of gestation and in 52 cases later in pregnancy. METHODS: All women were imaged on a 1.5 T clinical system using a single shot fast spin echo technique. The results of antenatal ultrasound and in utero magnetic resonance were compared. MAIN OUTCOME MEASURES: The definitive diagnosis was made either at autopsy or by postmortem magnetic resonance imaging, in cases that went to termination of pregnancy, or a combination of postnatal imaging and clinical follow up in the others. RESULTS: In 52 of cases, ultrasound and magnetic resonance gave identical results and in a further 12, magnetic resonance provided extra information that was judged not to have had direct effects on management. In 35 of cases, magnetic resonance either changed the diagnosis (29) or gave extra information that could have altered management (6). In 11 of the 30 cases where magnetic resonance changed the diagnosis, the brain was described as normal on magnetic resonance. CONCLUSIONS: In utero magnetic resonance imaging is a powerful tool in investigating fetal brain abnormalities. Our results suggest that in selected cases of brain abnormalities, detected by ultrasound, antenatal magnetic resonance may provide additional, clinically useful information that may alter management.


Assuntos
Encéfalo/anormalidades , Feto/anormalidades , Imageamento por Ressonância Magnética/métodos , Diagnóstico Pré-Natal/métodos , Feminino , Idade Gestacional , Humanos , Imageamento por Ressonância Magnética/normas , Gravidez , Diagnóstico Pré-Natal/normas , Estudos Prospectivos , Sensibilidade e Especificidade , Ultrassonografia Pré-Natal/métodos , Ultrassonografia Pré-Natal/normas
11.
Lancet ; 363(9412): 846-51, 2004 Mar 13.
Artigo em Inglês | MEDLINE | ID: mdl-15031028

RESUMO

BACKGROUND: Subdural haematomas are thought to be uncommon in babies born at term. This view is mainly based on findings in symptomatic neonates and babies in whom subdural haemorrhages are detected fortuitously. We aimed to establish the frequency of subdural haemorrhages in asymptomatic term neonates; to study the natural history of such subdural haematomas; and to ascertain which obstetric factors, if any, are associated with presence of subdural haematoma. METHODS: We did a prospective study in babies who were born in the Jessop wing of the Central Sheffield University Hospitals between March, 2001, and November, 2002. We scanned neonates with a 0.2 T magnetic resonance machine. FINDINGS: 111 babies underwent MRI in this study. 49 were born by normal vertex delivery without instrumentation, 25 by caesarean section, four with forceps, 13 ventouse, 18 failed ventouse leading to forceps, one failed ventouse leading to caesarean section, and one failed forceps leading to caesarean section. Nine babies had subdural haemorrhages: three were normal vaginal deliveries (risk 6.1%), five were delivered by forceps after an attempted ventouse delivery (27.8%), and one had a traumatic ventouse delivery (7.7%). All babies with subdural haemorrhage were assessed clinically but no intervention was needed. All were rescanned at 4 weeks and haematomas had completely resolved. INTERPRETATION: Presence of unilateral and bilateral subdural haemorrhage is not necessarily indicative of excessive birth trauma.


Assuntos
Hematoma Subdural/diagnóstico , Hematoma Subdural/epidemiologia , Índice de Apgar , Traumatismos do Nascimento/diagnóstico , Traumatismos do Nascimento/epidemiologia , Traumatismos do Nascimento/etiologia , Peso ao Nascer , Cesárea , Parto Obstétrico/efeitos adversos , Extração Obstétrica , Feminino , Hematoma Subdural/etiologia , Humanos , Recém-Nascido , Apresentação no Trabalho de Parto , Segunda Fase do Trabalho de Parto , Imageamento por Ressonância Magnética , Forceps Obstétrico , Gravidez , Estudos Prospectivos , Reino Unido/epidemiologia , Vácuo-Extração
12.
J Pediatr Surg ; 38(12): 1712-5, 2003 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-14666449

RESUMO

PURPOSE: Whereas endoscopic balloon dilatation (EBD) of benign esophageal strictures is an established mode of therapy in adults, this has not been accepted universally in the pediatric population. The aim of this study is to report the safety, efficacy, and long-term results of EBD for children in the authors' center. METHODS: Between 1986 and 2002, a total of 77 children (median age, 1.8 years; range, 2 months to 20 years) were treated by EBD for various causes: 2 had achalasia, and 75 had esophageal strictures (postesophageal atresia repair, 63; reflux esophagitis, 7; postfundoplication, 2; caustic injury, 3). Dilatations were performed using flexible endoscopy and fluoroscopic screening under general anesthesia. RESULTS: A total of 260 dilatations were carried out with the mean number of EBD per patient being 3.4 (range, 1 to 19). A mean period of 5 months (maximum, 28 months) for each patient was required. Four complications of esophageal perforations (1.5%) were observed, but only one required surgical repair because of persistent leakage. The remaining patients have undergone long-term follow-up (median follow-up, 6.6 years), and all are asymptomatic. CONCLUSIONS: This large series has shown that EBD can provide a safe and effective mean of relieving esophageal strictures with good long-term results.


Assuntos
Cateterismo , Estenose Esofágica/terapia , Adolescente , Cateterismo/efeitos adversos , Criança , Pré-Escolar , Perfuração Esofágica/etiologia , Humanos , Lactente , Estudos Retrospectivos , Resultado do Tratamento
13.
Arch Dis Child Fetal Neonatal Ed ; 88(3): F203-8, 2003 May.
Artigo em Inglês | MEDLINE | ID: mdl-12719393

RESUMO

BACKGROUND: Magnetic resonance (MR) imaging of the neonate has been restricted by the need to transport the sick baby to the large magnetic resonance scanners and often the need for sedation or anaesthesia in order to obtain good quality images. Ultrasound is the reference standard for neonatal imaging. OBJECTIVE: To establish a dedicated neonatal MR system and compare the clinical usefulness of MR imaging with ultrasound imaging. DESIGN: Prospective double blind trial. SETTING: Neonatal intensive care unit, Sheffield. MAIN OUTCOME MEASURES: Imaging reports. PATIENTS: 134 premature and term babies. RESULTS: In 56% of infants with pathology suspected on clinical grounds, MR provided additional useful clinical information over and above that obtained with ultrasound. CONCLUSION: Infants can be safely imaged by dedicated low field magnetic resonance on the neonatal intensive care unit without the need for sedation at a cost equivalent to ultrasound.


Assuntos
Encéfalo/anatomia & histologia , Recém-Nascido , Imageamento por Ressonância Magnética/métodos , Distribuição de Qui-Quadrado , Método Duplo-Cego , Ecoencefalografia , Idade Gestacional , Humanos , Recém-Nascido Prematuro/fisiologia , Estudos Prospectivos
14.
Hum Reprod ; 17(6): 1616-22, 2002 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12042287

RESUMO

BACKGROUND: This prospective observational study was undertaken to evaluate the reliability and consistency of ultrasound diagnosis of polycystic ovarian syndrome (PCOS). METHODS: Eighteen women with clinical and biochemical features suggestive of PCOS and nine normal control women underwent transvaginal ultrasound scan by a single ultrasonographer. The 27 ovarian scans were video-recorded and the recordings were later edited and arranged randomly so that each record appeared twice at random on the tape producing a total of 54 ovarian scans. Four experienced observers independently reviewed the recordings. The observers scored each case as follows: normal, possible polycystic ovary (PCO) and definite PCO. RESULTS: The mean intra-observer agreement was 69.4% (kappa = 0.54) and the mean inter-observer agreement was 51% (kappa = 0.28). CONCLUSION: The results suggest that the currently used ultrasonographic criteria for the diagnosis of polycystic ovaries do have significant intra-observer and inter-observer variability and as such must be considered subjective. Transvaginal ultrasonography alone may not therefore be a reliable method of diagnosing or excluding PCOS.


Assuntos
Síndrome do Ovário Policístico/diagnóstico por imagem , Adulto , Estudos de Casos e Controles , Erros de Diagnóstico , Feminino , Humanos , Variações Dependentes do Observador , Ultrassonografia , Gravação de Videoteipe
15.
Br J Radiol ; 75(890): 127-35, 2002 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-11893636

RESUMO

Iodixanol (Visipaque) is a dimeric, non-ionic iodinated contrast medium that is isotonic with blood at all clinically relevant concentrations. Iodixanol was compared in a randomized, double blind, parallel group, phase III multicentre trial with a monomeric, non-ionic contrast medium, iohexol (Omnipaque), at two concentrations assessing safety, tolerability and radiographic efficacy during contrast enhanced gastrointestinal radiography examinations of children. 154 children entered the trial; 152 formed the safety population and 147 the efficacy population. All examinations were performed following standard departmental practice. Children were assigned into either a high or low concentration group (iodixanol, 150 mgI ml(-1) and 320 mgI ml(-1) vs iohexol, 140 mgI ml(-1) and 300 mgI ml(-1)). The primary outcome measure for efficacy was the overall quality of visualization, which was assessed using a 100 mm visual analogue scale (VAS). The secondary efficacy variables assessed were quality of contrast opacification, mucosal coating and overall quality of diagnostic information. Safety evaluation involved patient follow-up for at least 48 h. Taste acceptance was also assessed. There was no statistically significant difference between the two contrast media with regard to the primary and secondary efficacy variables assessed, although higher ratings were observed for iodixanol. The 100 mm VAS score overall was 86 mm for iodixanol and 82 mm for iohexol (95% confidence interval -2.56, 10.42). The frequency of adverse events was lower for patients receiving iodixanol. Adverse events, mainly diarrhoea, occurred in 12 patients (16.2%) in the iodixanol group and 28 patients (35.9%) in the iohexol group. This reached statistical significance (p=0.006). Overall, iodixanol is well suited for examinations of the gastrointestinal tract, giving good efficacy results and fewer adverse events than iohexol.


Assuntos
Sistema Digestório/diagnóstico por imagem , Iohexol , Ácidos Tri-Iodobenzoicos , Adolescente , Criança , Pré-Escolar , Meios de Contraste/administração & dosagem , Meios de Contraste/efeitos adversos , Diarreia/induzido quimicamente , Relação Dose-Resposta a Droga , Método Duplo-Cego , Feminino , Humanos , Lactente , Recém-Nascido , Iohexol/administração & dosagem , Iohexol/efeitos adversos , Masculino , Radiografia , Ácidos Tri-Iodobenzoicos/administração & dosagem , Ácidos Tri-Iodobenzoicos/efeitos adversos
16.
BJOG ; 108(5): 519-26, 2001 May.
Artigo em Inglês | MEDLINE | ID: mdl-11368139

RESUMO

OBJECTIVE: To assess the ability of ultrafast magnetic resonance imaging to visualise abnormalities in the central nervous system of third trimester fetuses in utero and to compare the results with the current 'reference standard' of ultrasound and postnatal imaging or post-mortem data. DESIGN: A prospective, observational study comparing the diagnostic accuracy of two imaging methods: antenatal ultrasound and antenatal magnetic resonance with each other and postnatal or post mortem data. POPULATION: Twenty-one pregnant women of 19-36 weeks of gestation whose fetus were thought to have a central nervous system abnormality on the basis of antenatal ultrasound. The women had either not been offered or had refused a termination and were willing to have a magnetic resonance scan. METHODS: A 1.5T magnetic resonance scanner used a single shot fast spin echo sequence, in three image planes. The results were compared with the ultrasound results obtained by an experienced investigator independently. A series of 21 patients, with a range of pathologies of central nervous system, were imaged. Postnatal ultrasound and/or magnetic resonance imaging, or post-mortem data were used for additional confirmation of the pathology in all cases. RESULTS: The magnetic resonance report was different to the ultrasound in 10/21 (47.6%), magnetic resonance provided information additional to the ultrasound in 5/21 (23.8%), ultrasound and magnetic resonance results agreed in 6/21 cases (28.6%). CONCLUSION: Magnetic resonance in the third trimester provides a useful adjuvant to ultrasound imaging of the fetus when assessing abnormalities of the central nervous system after 19 weeks of gestation particularly if the abnormality involves the posterior fossa.


Assuntos
Encéfalo/anormalidades , Imageamento por Ressonância Magnética/métodos , Coluna Vertebral/anormalidades , Ultrassonografia Pré-Natal/métodos , Adolescente , Adulto , Feminino , Humanos , Imageamento por Ressonância Magnética/normas , Gravidez , Segundo Trimestre da Gravidez , Terceiro Trimestre da Gravidez , Estudos Prospectivos , Ultrassonografia Pré-Natal/normas
18.
Cleft Palate Craniofac J ; 37(2): 166-71, 2000 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-10749057

RESUMO

OBJECTIVE: This investigation was performed to determine if an easily measurable, reproducible, bony parameter could be identified that might predict hearing loss in cleft palate children. SUBJECTS: In this prospective study performed at the Sheffield Children's Hospital (U.K.), 34 children with successfully repaired cleft palate who responded to a postal request for volunteers were assessed clinically, audiologically, and by lateral soft tissue neck radiography. Six children were excluded because of previous otologic surgery or poor quality radiographs. Twenty-six children who had the same series of investigations were randomly selected from routine otolaryngological outpatient clinics and acted as controls. METHODS: The sphenopalatine angle (SPA), which relates the facial and cranial components of the skull, was measured on each child's radiograph. RESULTS: The median SPA in the cleft palate group was significantly greater than in the control group (p = 0.01). In those cleft palate children with a hearing loss the sphenopalatine angle was smaller than in their normal hearing counterparts (p = 0.01). No significant difference was found in the SPA between the hearing loss and normal hearing controls. There was no significant difference in age ranges between the hearing and hearing loss subgroups in each of the two primary groups. CONCLUSIONS: In this study, those cleft palate children with a smaller SPA have a greater incidence of hearing loss.


Assuntos
Fissura Palatina/complicações , Perda Auditiva Condutiva/etiologia , Perda Auditiva Condutiva/patologia , Base do Crânio/patologia , Estudos de Casos e Controles , Cefalometria , Criança , Pré-Escolar , Tuba Auditiva/fisiopatologia , Humanos , Otite Média com Derrame/complicações , Otite Média com Derrame/etiologia , Palato/diagnóstico por imagem , Palato/patologia , Estudos Prospectivos , Radiografia , Reprodutibilidade dos Testes , Base do Crânio/diagnóstico por imagem , Osso Esfenoide/diagnóstico por imagem , Osso Esfenoide/patologia , Estatísticas não Paramétricas
19.
Pediatr Radiol ; 29(11): 835-7, 1999 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-10552063

RESUMO

We report two brothers with a new type of lethal, micromelic, short-rib, skeletal dysplasia characterised by short limbs with distinctive triangular-shaped humeri. This condition is most likely caused by either an autosomal recessive or X-linked recessive gene.


Assuntos
Doenças do Desenvolvimento Ósseo/genética , Úmero/anormalidades , Doenças do Desenvolvimento Ósseo/diagnóstico por imagem , Morte Fetal , Genes Recessivos , Humanos , Recém-Nascido , Masculino , Radiografia , Síndrome de Costela Curta e Polidactilia/genética , Síndrome
20.
Skeletal Radiol ; 27(9): 515-7, 1998 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-9809882

RESUMO

We report on a 13-year-old boy who had a slipped capital femoral epiphysis and was found to have type II benign autosomal dominant osteopetrosis. This association has not previously been reported.


Assuntos
Epifise Deslocada/etiologia , Osteopetrose/complicações , Adolescente , Epifise Deslocada/diagnóstico por imagem , Epifise Deslocada/cirurgia , Cabeça do Fêmur/cirurgia , Humanos , Masculino , Osteopetrose/diagnóstico por imagem , Radiografia
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