Congenital diaphragmatic eventration and hernia sac compared to CDH with true defects: a retrospective cohort study.

Abstract:

:Congenital diaphragmatic eventration (CDE) and congenital diaphragmatic hernia (CDH) with or without hernia sac are three different types of congenital diaphragmatic malformations, which this study evaluates. All surgically treated patients with CDE or Bochdalek type CDH between 2000 and 2016 were included in this retrospective analysis. Demographics, CDH-characteristics, treatment, and clinical outcome were evaluated. In total, 200 patients were included. Patients with an eventration or hernia sac had no significant differences and were compared as patients without a true defect to patients with a true defect. The 1-year survival of patients with a true defect was significantly lower than patients with no true defect (76% versus 97%, p = 0.001). CDH with no true defect had significantly better short-term outcomes than CDH with true defect requiring patch repair. However, at 30 days, they more often required oxygen supplementation (46% versus 26%, p = 0.03) and had a higher recurrence rate (8% versus 0%, p = 0.006) (three eventration and two hernia sac patients). Conclusion: Patients without a true defect seem to have a more similar clinical outcome than CDH patients with a true defect, with a better survival. However, the recurrence rate and duration of oxygen supplementation at 30 days are higher than CDH patients with a true defect.What is Known:• Congenital diaphragmatic hernia with or without hernia sac and congenital diaphragmatic eventration (incomplete muscularization) are often treated similarly.• Patients with hernia sac and eventration are thought to have a relatively good outcome, but exact numbers are not described.What is New:• Congenital diaphragmatic eventration and patients with hernia sac seem to have a more similar clinical outcome than Bochdalek type CDH with a true defect.• Patients without a true defect (eventration or hernia sac) have a high recurrence rate.

journal_name

Eur J Pediatr

authors

Heiwegen K,van Heijst AF,Daniels-Scharbatke H,van Peperstraten MC,de Blaauw I,Botden SM

doi

10.1007/s00431-020-03576-w

subject

Has Abstract

pub_date

2020-06-01 00:00:00

pages

855-863

issue

6

eissn

0340-6199

issn

1432-1076

pii

10.1007/s00431-020-03576-w

journal_volume

179

pub_type

杂志文章
  • Ultrasonography after the first febrile urinary tract infection in children.

    abstract:UNLABELLED:The importance of ultrasonography after the first febrile urinary tract infection has been recently challenged. The aim of this study was to evaluate the role of ultrasonography in detection of significant non-reflux abnormalities in the kidneys and the urinary tract, and to determine whether these findings ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-006-0113-4

    authors: Jahnukainen T,Honkinen O,Ruuskanen O,Mertsola J

    更新日期:2006-08-01 00:00:00

  • Monogenic forms of hypertension.

    abstract::Arterial hypertension in childhood is less frequent as compared to adulthood but is more likely to be secondary to an underlying disorder. After ruling out more obvious causes, some patients still present with strongly suspected secondary hypertension of yet unknown etiology. A number of these children have hypertensi...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章,评审

    doi:10.1007/s00431-011-1440-7

    authors: Simonetti GD,Mohaupt MG,Bianchetti MG

    更新日期:2012-10-01 00:00:00

  • Somatic symptom and related disorders in a tertiary paediatric hospital: prevalence, reach and complexity.

    abstract::Specialist paediatric services manage a variety of presentations of functional somatic symptoms. We aimed to describe the presentation and management of children and adolescents with somatic symptom and related disorders (SSRDs) requiring admission to a tertiary children's hospital with the objective of informing the ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-020-03867-2

    authors: Wiggins A,Court A,Sawyer SM

    更新日期:2020-11-13 00:00:00

  • Risk factors for hyperbilirubinemia in breastfed term neonates.

    abstract:UNLABELLED:Increased breastfeeding was suggested as a contributing factor to significant hyperbilirubinemia. The aim of this study was to identify the risk factors associated with jaundice in exclusively breastfed term neonates. We retrospectively reviewed all consecutively live-born neonates from August 2009 to July 2...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-011-1512-8

    authors: Chen YJ,Chen WC,Chen CM

    更新日期:2012-01-01 00:00:00

  • Physical symptoms in very young children assessed for sexual abuse: a mixed method analysis from the ASAC study.

    abstract::So far, a recognizable pattern of clinical symptoms for child sexual abuse (CSA), especially in young male children, is lacking. To improve early recognition of CSA, we reviewed physical complaints, physical examination, and tests on sexually transmitted infections (STIs) in confirmed victims (predominantly preschool ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-017-2996-7

    authors: Vrolijk-Bosschaart TF,Brilleslijper-Kater SN,Widdershoven GA,Teeuw ARH,Verlinden E,Voskes Y,van Duin EM,Verhoeff AP,Benninga MA,Lindauer RJL

    更新日期:2017-10-01 00:00:00

  • Complex regional pain syndrome involving the face following snowball injury.

    abstract::Complex regional pain syndrome (CRPS) is a condition of unknown etiology characterized by autonomic, sensory, and motor disturbance. CRPS usually follows an injury in the affected limb, which is often trivial in nature. CRPS involving the facial region is rare, and there have been no previous descriptions in children....

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-013-2159-4

    authors: Goenka A,Aziz M,Riley P,Vassallo G

    更新日期:2014-03-01 00:00:00

  • Clinical characteristics of children with hypoparathyroidism due to 22q11.2 microdeletion.

    abstract:UNLABELLED:The phenotypes of chromosomal 22q11.2 microdeletion are quite variable among individuals and hypoparathyroidism (HP) constitutes a definite portion of the clinical spectrum. For the correct diagnosis and pertinent follow up of the HP children due to del22q11.2, we tried to delineate the clinical characterist...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s004310050762

    authors: Adachi M,Tachibana K,Masuno M,Makita Y,Maesaka H,Okada T,Hizukuri K,Imaizumi K,Kuroki Y,Kurahashi H,Suwa S

    更新日期:1998-01-01 00:00:00

  • Subependymal pseudocysts in the neonate.

    abstract::Serial ultrasound examinations were performed through the anterior fontanelle to detect and follow subependymal pseudocysts (SP) in 19 neonates without severe malformations. A high-resolution real-time sector scanner was employed. In 8 cases the SP involved both lateral ventricles, in 11 cases they were unilateral and...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00595915

    authors: Zorzi C,Angonese I

    更新日期:1989-02-01 00:00:00

  • The influence of perinatal risk factors on the incidence of atypical coagulation factor VII during the first days of life.

    abstract::The correlation between the appearance of functionally-atypical factor VII and perinatal complications was investigated in 66 newborn infants. The presence of an abnormal clotting factor was assumed if the ratio between clotting activity and antigen-related factor VII material exceeded the normal range for adult plasm...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00493570

    authors: Maak B,Frenzel J

    更新日期:1977-08-12 00:00:00

  • Coexistence of polyarteritis nodosa and psoriatic arthritis in a child: an unreported association: Polyarteritis nodosa and Psoriatic arthitritis.

    abstract::Polyarteritis nodosa (PAN) is a non-frequent vasculitis of small- and medium-sized vessels. Psoriatic arthritis (PA) is described as a "unique inflammatory arthritis associated with psoriasis" with an inexact prevalence rate due to the lack of widely accepted classification criteria. We describe the case of an 11-year...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-011-1459-9

    authors: Oulego-Erroz I,Gautreaux-Minaya S,Martinez-Sáenz de Jubera J,Naranjo-Vivas D,Fernéndez-Hernández S,Muñíz-Fontán M

    更新日期:2011-09-01 00:00:00

  • The impact of diet, body composition, and physical activity on child bone mineral density at five years of age-findings from the ROLO Kids Study.

    abstract::Bone health is extremely important in early childhood because children with low bone mineral density (BMD) are at a greater risk of bone fractures. While physical activity and intake of both calcium and vitamin D benefit BMD in older children, there is limited research on the determinants of good bone health in early ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-019-03465-x

    authors: McVey MK,Geraghty AA,O'Brien EC,McKenna MJ,Kilbane MT,Crowley RK,Twomey PJ,McAuliffe FM

    更新日期:2020-01-01 00:00:00

  • Sodium valproate versus phenobarbital in the prophylactic treatment of febrile convulsions in childhood.

    abstract::Phenobarbital has been shown to offer effective prophylaxis against childhood febrile convulsions. However, a high percentage of children do not tolerate phenobarbital, mainly due to behavioral changes. Valproate, due to its low toxicity, appears to be an attractive alternative to phenobarbital treatment. Ninety child...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00441308

    authors: Lee K,Melchior JC

    更新日期:1981-10-01 00:00:00

  • Structural alteration of the insulin-like growth factor II-gene in Wilms tumour.

    abstract::In this study messenger ribonucleic acid (mRNA) and DNA of five Wilms tumours were investigated. As expected, the level of insulin-like growth factor (IGF) II-mRNA was elevated up to 50 times in tumour tissue as compared to normal adjacent kidney tissue. In addition, genomic DNA was isolated and digested with appropri...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章,评审

    doi:10.1007/BF00441514

    authors: Irminger JC,Schoenle EJ,Briner J,Humbel RE

    更新日期:1989-06-01 00:00:00

  • Urinary oligosaccharide screening in patients with beta-galactosidase deficiency.

    abstract::Following ion-exchange chromatography and subsequent thin-layer chromatography, 3 peculiar oligosaccharide excretion patterns were distinguished in 3 patients with beta-galactosidase deficiency. Each patient differed clinically and it is proposed that this method may be of use in characterizing various forms of beta-g...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00496087

    authors: Sewell AC,Gehler J,Spranger J

    更新日期:1980-05-01 00:00:00

  • Age-associated differences in prevalence of group A streptococcal type-specific M antibodies in children.

    abstract::Our prior studies of the molecular epidemiology of group A streptococcus (GAS) pharyngitis indicated that the most common emm types associated with pediatric pharyngitis in North America were 12, 1, 28, and 4. We previously reported that the proportions of pediatric pharyngitis due to emm types 12 and 4 decreased with...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-008-0819-6

    authors: Jaggi P,Dale JB,Chiang E,Beniwal P,Kabat W,Shulman ST

    更新日期:2009-06-01 00:00:00

  • Final height and puberty in 40 patients after antileukaemic treatment during childhood.

    abstract:UNLABELLED:Endocrine dysfunction and damage of the epiphysial growth plates have been reported as late effects of antileukaemic treatment during childhood. It is a common opinion that cranial irradiation (CI) is the most important factor for blunted growth. Accordingly, recent therapeutic strategies in acute lymphoblas...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s004310050599

    authors: Mohnike K,Dörffel W,Timme J,Kluba U,Aumann V,Vorwerk P,Mittler U

    更新日期:1997-04-01 00:00:00

  • Mitral valve prolapse in Turner syndrome.

    abstract::We have evaluated 46 patients with Turner syndrome by clinical examination, M-mode and two-dimensional echocardiography, dynamic exercise testing and 24 h Holter monitoring. Twelve patients (26.1%) had mitral valve prolapse and 7 patients (15.2%) had isolated non stenotic bicuspid aortic valve. Aortic root dilation wa...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00441551

    authors: Bastianon V,Pasquino AM,Giglioni E,Bosco G,Tebaldi L,Cives C,Colloridi V

    更新日期:1989-04-01 00:00:00

  • Brugada syndrome in childhood: a potential fatal arrhythmia not always recognised by paediatricians. A case report and review of the literature.

    abstract::We report on a youngster followed by his paediatrician from birth until 14 years of age for premature beats, most likely of ventricular origin. The sudden death of his sister provoked a re-assessment of his electrocardiograms (ECG), resulting in the diagnosis of Brugada syndrome and the subsequent implantation of a ca...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章,评审

    doi:10.1007/s00431-006-0150-z

    authors: Mivelaz Y,Di Bernardo S,Pruvot E,Meijboom EJ,Sekarski N

    更新日期:2006-08-01 00:00:00

  • Effects of levothyroxine therapy on left and right ventricular function in neonates with congenital hypothyroidism: a tissue Doppler echocardiography study.

    abstract::Cardiac function is impaired in adults or children with hypothyroidism and it can be reversed by levothyroxine (L-T(4)) substitution therapy. However, only a few studies are available on left and right ventricular function in neonates with congenital hypothyroidism (CH), most of which were performed with standard echo...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-007-0417-z

    authors: Mao S,Wang Y,Jiang G,Zhao Z

    更新日期:2007-12-01 00:00:00

  • Impact of ventricular arrhythmias on outcomes in children with myocarditis.

    abstract::Children affected with acute myocarditis may progress rapidly into profound ventricular dysfunction and ventricular arrhythmias. The objective of this study is to assess the impact of ventricular arrhythmias on in-hospital mortality and the use of mechanical circulatory support in patients with myocarditis. Pediatric ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-020-03687-4

    authors: Othman HF,Byrnes J,Elsamny E,Hamzah M

    更新日期:2020-11-01 00:00:00

  • Investigation of the nutritional state of children in a Congolese village. II. Plasma fatty acid composition.

    abstract::The fatty acid status of an unselected group of 84 Congolese children was determined by estimating the fatty acid composition of the plasma phospholipid (PL) and cholesterolester (CE) fractions using capillary gas chromatography. In comparison with North American and European children a wide range of values and low me...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00445928

    authors: Leichsenring M,Doehring-Schwerdtfeger E,Laryea MD,Diamouangana J,Bremer HJ

    更新日期:1988-11-01 00:00:00

  • Desquamative interstitial pneumonitis and alveolar lipoproteinosis: diagnostic difficulties and therapy problems with an infant.

    abstract::A desquamative, interstitial pneumonitis was diagnosed histologically in a 9-month-old boy who first became ill at the age of 5 weeks. The desquamative interstitial pneumonitis was associated with an acquired cytomegalovirus (CMV) infection. Despite treatment with corticoids, acyclovir and artificial ventilation, the ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF02429072

    authors: Schneider K,Brünstler I,Vogel H,Fendel H,Remberger K

    更新日期:1986-12-01 00:00:00

  • The Dubowitz syndrome.

    abstract::The Dubowitz syndrome is a rare, autosomal, recessively inherited disorder of intrauterine and postnatal growth retardation leading to microcephaly, moderate mental retardation and such characteristic facial anomalies as telecanthus, epicanthic folds, blepharophimosis, ptosis, broadening of the bridge and tip of the n...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00496039

    authors: Küster W,Majewski F

    更新日期:1986-04-01 00:00:00

  • Clinical usefulness of high intensity green light phototherapy in the treatment of neonatal jaundice.

    abstract::Two matched groups of term newborn infants with idiopathic jaundice were subjected to intensive double direction green or blue light phototherapy (PT). The efficacy of treatment was expressed as rate of decline of serum bilirubin concentration after 6, 12 and 24 h of light exposure. More rapid response was obtained us...

    journal_title:European journal of pediatrics

    pub_type: 临床试验,杂志文章

    doi:10.1007/BF01955530

    authors: Amato M,Inaebnit D

    更新日期:1991-02-01 00:00:00

  • Preliminary neuropsychological test results.

    abstract::A series of information processing tasks was administered to 22 PKU children aged 8.5 years who had been under dietary treatment since birth as well as to 20 controls of the same age. This contribution presents the results of two tasks from this series: a continuous performance task and a calculation task. The continu...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF02126298

    authors: de Sonneville LM,Schmidt E,Michel U,Batzler U

    更新日期:1990-01-01 00:00:00

  • Coombs-positive giant cell hepatitis of infancy: effect of steroids and azathioprine therapy.

    abstract::An 8-month-old boy and a 7-month-old girl presented with an acute, Coombs-positive auto-immune haemolytic anaemia and severe hepatitis. The clinical manifestations were pallor, jaundice and hepatomegaly. The liver histology revealed diffuse giant cell transformation and extensive necrosis with central-portal bridging....

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF01955929

    authors: Brichard B,Sokal E,Gosseye S,Buts JP,Gadisseux JF,Cornu G

    更新日期:1991-03-01 00:00:00

  • Visual acuity and stereopsis between the ages of 5 and 10 years. A cross-sectional study.

    abstract::The development of visual acuity and stereopsis was studied in 321 boys and 340 girls aged between 5 and 10 years. Visual acuity was assessed by the E test and a modified version of the STYCAR test, stereo acuity by the Lang-Stereo test [17]. Both vision tests showed an increase in the median visual acuity between the...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF02429046

    authors: Schmid M,Largo RH

    更新日期:1986-12-01 00:00:00

  • Long-term outcomes in pediatric appendiceal carcinoids: Turkey experience.

    abstract::The tendency of non-operative management of appendicitis let us explore the natural history of appendiceal carcinoids, compare them with appendicitis patients, and determine the possibility of deciding the extent of the surgery and post-operative follow-up on behalf of the intraoperative findings. A retrospective revi...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-018-3258-z

    authors: Akova F,Aydin E,Nur Eray Y,Toksoy N,Yalcin S,Altinay S,Tetikkurt US

    更新日期:2018-12-01 00:00:00

  • A patient with Dent disease and features of Bartter syndrome caused by a novel mutation of CLCN5.

    abstract:UNLABELLED:Dent disease is an X-linked tubulopathy mainly caused by inactivating mutations of CLCN5. Features of Bartter syndrome such as hypokalemic metabolic alkalosis are rarely observed in patients with Dent disease. We report a Japanese male patient with Dent disease who also manifested features of Bartter syndrom...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-011-1578-3

    authors: Okamoto T,Tajima T,Hirayama T,Sasaki S

    更新日期:2012-02-01 00:00:00

  • Cardiac involvement in glycogen storage disease type III.

    abstract::Twenty patients with enzymatically proven glycogen storage disease type III (GSD III) aged 3-30 years underwent cardiological evaluation. Seventeen showed subclinical evidence of cardiac involvement in form of ventricular hypertrophy on ECG. Of 16 patients in whom an ECG examination was performed, 13 had abnormal echo...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00443106

    authors: Moses SW,Wanderman KL,Myroz A,Frydman M

    更新日期:1989-08-01 00:00:00