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1.
Ann Thorac Surg ; 114(2): e105-e107, 2022 08.
Article in English | MEDLINE | ID: mdl-34896089

ABSTRACT

Pectus arcuatum presents with sternal angle protrusion and bilateral cartilage deformity. A modified Ravitch procedure is the most common surgical approach. A graft to fill up the osteotomy may be necessary to ensure a stable correction. Studies of the behavior of a cartilage graft transplanted to a human bone defect are scarce. We present a case of autologous rib cartilage graft for sternotomy stabilization during pectus arcuatum repair. Graft viability and new bone formation were proved by computed tomography. Autologous cartilage rib graft is a biocompatible substitute available in the same surgical field with satisfactory results and minimal morbidity.


Subject(s)
Funnel Chest , Thoracic Wall , Cartilage/surgery , Funnel Chest/surgery , Humans , Osteotomy/methods , Sternum/surgery
2.
J Pediatr Urol ; 17(3): 401.e1-401.e9, 2021 06.
Article in English | MEDLINE | ID: mdl-33663999

ABSTRACT

INTRODUCTION: Since the first case of dextranomer/hyaluronic acid (Dx/HA) implant calcification in 2008, concern about the long-term sequelae of Dx/HA injection has been growing. According to previous reports, the incidence of Dx/HA calcification 4 years after injection would be around 2%. AIM: The primary aim was to estimate the incidence of Dx/HA implant calcification after endoscopic treatment of vesicoureteral reflux in pediatric patients. Secondary objectives were to establish risk factors and to perform a survival analysis after Dx/HA injection. STUDY DESIGN: Patients undergoing Dx/HA endoscopic injection from 2007 to 2014 were prospectively registered. The database included clinical, surgical and radiological outcomes. Patients that showed Dx/HA implant calcification during follow-up were compared to those who did not. Univariable and survival statistical analyses were performed. RESULTS: 30 implants calcified over 355 ureters endoscopically treated. Age at first treatment was lower in patients with implant calcification (2.4 ± 1.3 years vs 3.6 ± 2.5 years; p < 0.005). The risk of implant calcification was 8.45% (95% CI: 5.96-11.85%). Median follow-up was 7.6 years (IQR: 5.2-9.5). The incidence rate was 12.06 cases per 1000 ureters-year. The period of highest hazard of implant calcification was between 3 and 5 years after injection. The only risk factor related to implant calcification was the age at first injection: relative risk of implant calcification was 4.4 (95% CI: 1.6 to 12.4; p = 0.002) for patients first treated before the age of 3.5 years. DISCUSSION: The risk and the incidence rate of Dx/HA implant calcification were higher than previous data. The period of highest hazard and detection of implant calcification were consistent with previous reports. Patients first treated before the age of 3.5 had shorter survival time without implant calcification. These are the first data about risk factors and survival function of Dx/HA implant calcification. However, our conclusions about the clinical significance of Dx/HA implant calcification were limited because the patients with implant calcification were asymptomatic. Further studies with larger sample and longer follow-up should confirm the clinical significance and life-long tendency of Dx/HA implant calcification. CONCLUSIONS: The risk and the incidence rate of Dx/HA implant calcification were higher than expected. The hazard of calcification was higher between 3 and 5 years after injection. The risk was especially higher in patients treated before the age of 3.5. Caution should be taken not to confuse implant calcifications with ureteric stones. A 5-year follow-up would set a better understanding of the actual incidence and clinical significance of implant calcification.


Subject(s)
Hyaluronic Acid , Vesico-Ureteral Reflux , Child , Child, Preschool , Dextrans/adverse effects , Humans , Hyaluronic Acid/adverse effects , Incidence , Risk Factors , Vesico-Ureteral Reflux/epidemiology , Vesico-Ureteral Reflux/therapy
3.
Pediatr Surg Int ; 37(1): 59-65, 2021 Jan.
Article in English | MEDLINE | ID: mdl-33245446

ABSTRACT

PURPOSE: Recurrence of congenital diaphragmatic hernia (CDH) is a treatment-related morbidity which can be preventable. There is no consensus about the ideal material for diaphragmatic substitution. The aim of our study is to identify if the use of porcine dermis patches increases the risk of CDH recurrence. METHODS: Retrospective review of medical records of CDH patients treated between 2013 and 2017 in our center was carried out. Demographic, clinical and surgical variables were collected. Regression analysis was performed to identify which factors increase the risk of recurrence. RESULTS: 50 patients entered the study. 94% of the patients had a left CDH, mean observed/expected lung-to-head ratio was 46%. 17 patients underwent a primary closure, the rest a patch closure: 25 Gore-Tex® and 8 porcine dermis patches were used. Seven patients presented recurrence (14%). Median follow-up time was 3.5 years (1.2-6.2). Univariate analysis revealed that the use of a porcine dermis patch (75%) increased the risk of recurrence compared with Gore-Tex® patch (4%) and primary closure (0%) p < 0.001 (HR 58.7; IC 95%: 6.9-501.2; p < 0.001). CONCLUSION: The main risk factor for CDH recurrence is the use of a porcine dermis patch. We do not recommend the use of these patches for CDH repair.


Subject(s)
Biocompatible Materials/therapeutic use , Hernias, Diaphragmatic, Congenital/surgery , Herniorrhaphy/instrumentation , Herniorrhaphy/methods , Surgical Mesh , Animals , Causality , Cohort Studies , Female , Follow-Up Studies , Humans , Infant, Newborn , Male , Polytetrafluoroethylene , Recurrence , Retrospective Studies , Risk Factors , Swine , Treatment Outcome
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