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  1. Article ; Online: Central Nervous System Metastases in Pediatric Patients With Ewing Sarcoma.

    Slatnick, Leonora R / Cost, Carrye / Garrington, Timothy / Donaldson, Nathan / Macy, Margaret E

    Journal of pediatric hematology/oncology

    2024  Volume 46, Issue 2, Page(s) e180–e183

    Abstract: Metastatic central nervous system (CNS) involvement is rare in pediatric primary extracranial Ewing sarcoma (ES). We describe the incidence and course of 6 patients with extracranial ES who developed metastatic CNS lesions treated at a single institution. ...

    Abstract Metastatic central nervous system (CNS) involvement is rare in pediatric primary extracranial Ewing sarcoma (ES). We describe the incidence and course of 6 patients with extracranial ES who developed metastatic CNS lesions treated at a single institution. The median time to CNS disease detection was 16.3 months (10.0-28.3 months). Event-free and overall survival after CNS disease detection were 1.9 months (0.4 to 10.3 months) and 4.6 months (1.1 to 50.9 months), respectively. One patient was alive at the time of analysis. Clinical status and ability to obtain disease control should be considered when making decisions regarding aggressive interventions in these patients with poor prognosis.
    MeSH term(s) Child ; Humans ; Sarcoma, Ewing/pathology ; Central Nervous System Neoplasms/therapy ; Central Nervous System Neoplasms/secondary ; Incidence ; Neoplasms, Second Primary ; Retrospective Studies ; Central Nervous System Diseases ; Central Nervous System/pathology
    Language English
    Publishing date 2024-02-02
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1231152-2
    ISSN 1536-3678 ; 1077-4114 ; 0192-8562
    ISSN (online) 1536-3678
    ISSN 1077-4114 ; 0192-8562
    DOI 10.1097/MPH.0000000000002825
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Acute Hematogenous Bacterial Osteoarticular Infections in Children.

    Donaldson, Nathan / Sanders, Julia / Child, Jason / Parker, Sarah

    Pediatrics in review

    2020  Volume 41, Issue 3, Page(s) 120–136

    MeSH term(s) Anti-Bacterial Agents/therapeutic use ; Arthritis, Infectious/drug therapy ; Bacterial Infections ; Child ; Child, Preschool ; Female ; Humans ; Male ; Osteomyelitis/drug therapy
    Chemical Substances Anti-Bacterial Agents
    Language English
    Publishing date 2020-05-11
    Publishing country United States
    Document type Journal Article
    ZDB-ID 774515-1
    ISSN 1526-3347 ; 0191-9601
    ISSN (online) 1526-3347
    ISSN 0191-9601
    DOI 10.1542/pir.2018-0201
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Identifying predictors for source culture positivity in children with acute musculoskeletal infections.

    MacBrayne, Christine E / DeVine, Mackenzie N / Pearce, Kelly / Donaldson, Nathan / Parker, Sarah K / Searns, Justin B

    Diagnosis (Berlin, Germany)

    2022  Volume 9, Issue 3, Page(s) 359–363

    Abstract: Objectives: Identifying the causative bacterial pathogen for children with acute hematogenous musculoskeletal infections (MSKIs) allows for improved care. The purpose of our study was to determine if clinical markers could predict which patients will ... ...

    Abstract Objectives: Identifying the causative bacterial pathogen for children with acute hematogenous musculoskeletal infections (MSKIs) allows for improved care. The purpose of our study was to determine if clinical markers could predict which patients will have a causative pathogen found on source culture alone, thus being highest yield to undergo operative diagnostic procedures.
    Methods: A single-center, retrospective cohort study was performed. Medical records for patients between 6 months and 18 years of age admitted between July 2014 and September 2018 with a discharge diagnosis of acute osteomyelitis, septic arthritis, or pyomyositis were reviewed. Patients were stratified based on results of blood and source cultures. Predictors of interest were screened on a univariable basis with significant predictors retained in a multivariate analysis.
    Results: There were 170 patients included. No predictors were significantly associated with increased odds of having a causative pathogen found on source culture alone. Degree of C-reactive protein elevation and history of fever were associated with decreased odds of being source culture positive, OR (95% CI); 0.92 (0.87, 0.98) and 0.39 (0.19, 0.81), respectively.
    Conclusions: Predictive modeling failed to identify children with MSKIs whose causative pathogen was found by source culture alone. It is difficult to predict which MSKI patients will be highest yield for operative diagnostic procedures.
    MeSH term(s) Arthritis, Infectious/complications ; Arthritis, Infectious/diagnosis ; Arthritis, Infectious/microbiology ; Child ; Humans ; Infections ; Osteomyelitis/complications ; Osteomyelitis/diagnosis ; Osteomyelitis/microbiology ; Pyomyositis/complications ; Pyomyositis/diagnosis ; Pyomyositis/microbiology ; Retrospective Studies
    Language English
    Publishing date 2022-05-30
    Publishing country Germany
    Document type Journal Article
    ISSN 2194-802X
    ISSN (online) 2194-802X
    DOI 10.1515/dx-2021-0155
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Characteristics of Children With Culture Negative Acute Hematogenous Musculoskeletal Infections.

    Searns, Justin B / DeVine, Mackenzie N / MacBrayne, Christine E / Williams, Manon C / Pearce, Kelly / Donaldson, Nathan / Parker, Sarah K

    Journal of pediatric orthopedics

    2022  Volume 42, Issue 2, Page(s) e206–e211

    Abstract: Background: Identifying the causative pathogen for acute hematogenous musculoskeletal infections (MSKIs) allows for directed antimicrobial therapy and diagnostic confidence. However, 20% to 50% of children with acute MSKIs remain culture negative. The ... ...

    Abstract Background: Identifying the causative pathogen for acute hematogenous musculoskeletal infections (MSKIs) allows for directed antimicrobial therapy and diagnostic confidence. However, 20% to 50% of children with acute MSKIs remain culture negative. The objective of this study was to compare characteristics of culture negative MSKI patients to those where a pathogen is identified.
    Methods: Electronic medical records of children admitted between July 2014 to September 2018 to a single quaternary care pediatric hospital with acute MSKIs were retrospectively reviewed. Clinical and demographic characteristics were compared between culture positive and culture negative MSKIs.
    Results: A total of 170 patients were included of whom 43 (25%) were culture negative. All culture negative patients had at least 1 culture type obtained, and the majority (84%) had both blood and source cultures performed. When compared with patients with a causative pathogen identified, culture negative patients were younger (2.3 vs. 9.8 y), smaller (13.5 vs. 31.6 kg), less likely to be febrile on arrival (56% vs. 77%), less likely to have an abscess on imaging (23% vs. 48%), and were more likely to have uncomplicated septic arthritis (35% vs. 8%). No critically ill patient was culture negative. Seven culture negative patients had additional Kingella kingae testing performed, none of which were positive.
    Conclusions: Despite targeted and standardized efforts to identify causative bacteria, 25% of children with acute MSKIs never have a pathogen identified. Culture negative patients are younger, less febrile, are less likely to have an abscess, and more likely to have isolated septic arthritis.
    Level of evidence: This is a retrospective cohort study interested in identifying patient characteristics that predict rate of culture positivity for acute MSKIs. This study meets criteria for Level II evidence.
    MeSH term(s) Anti-Bacterial Agents/therapeutic use ; Arthritis, Infectious/diagnosis ; Arthritis, Infectious/drug therapy ; Arthritis, Infectious/epidemiology ; Child ; Humans ; Infant ; Kingella kingae ; Musculoskeletal System ; Osteomyelitis/drug therapy ; Retrospective Studies
    Chemical Substances Anti-Bacterial Agents
    Language English
    Publishing date 2022-01-06
    Publishing country United States
    Document type Journal Article
    ZDB-ID 604642-3
    ISSN 1539-2570 ; 0271-6798
    ISSN (online) 1539-2570
    ISSN 0271-6798
    DOI 10.1097/BPO.0000000000002033
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Synovial Cell Sarcoma in an Adolescent Liver Transplant Recipient.

    Jaramillo, Catalina / Gilani, Ahmed / Haag, Mary / Donaldson, Nathan / Mack, Cara

    ACG case reports journal

    2019  Volume 6, Issue 5, Page(s) e00091

    Abstract: Solid organ transplant recipients are at increased risk of malignancy. Pediatric transplant recipients particularly have a potentially higher risk given the young age of immunosuppression initiation. Posttransplant malignancies are the main cause of ... ...

    Abstract Solid organ transplant recipients are at increased risk of malignancy. Pediatric transplant recipients particularly have a potentially higher risk given the young age of immunosuppression initiation. Posttransplant malignancies are the main cause of death in 5%-16% of liver transplantation patients. The frequency of de novo malignancies in pediatric liver transplant recipients has been reported to be 13%. Synovial sarcoma is a malignant mesenchymal neoplasm that has not been previously reported after liver transplantation. We report the case of an adolescent liver transplant recipient who was diagnosed with synovial sarcoma 14 years after liver transplantation.
    Language English
    Publishing date 2019-05-16
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2814825-3
    ISSN 2326-3253
    ISSN 2326-3253
    DOI 10.14309/crj.0000000000000091
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Single cell RNA-sequencing of Ewing sarcoma tumors demonstrates transcriptional heterogeneity and clonal evolution.

    Goodspeed, Andrew / Bodlak, Avery / Nelson-Taylor, Sarah / Oike, Naoki / Porfilio, Timothy / Shirai, Ryota / Walker, Deandra / Treece, Amy / Black, Jennifer / Donaldson, Nathan / Cost, Carrye / Garrington, Tim / Greffe, Brian / Luna-Fineman, Sandra / Demedis, Jenna / Lake, Jessica / Danis, Etienne / Verneris, Michael / Hayashi, Masanori

    bioRxiv : the preprint server for biology

    2024  

    Abstract: Ewing sarcoma is the second most common bone cancer in children, accounting for 2% of pediatric cancer diagnoses. Patients who present with metastatic disease at the time of diagnosis have a dismal prognosis, compared to the >70% 5-year survival of those ...

    Abstract Ewing sarcoma is the second most common bone cancer in children, accounting for 2% of pediatric cancer diagnoses. Patients who present with metastatic disease at the time of diagnosis have a dismal prognosis, compared to the >70% 5-year survival of those with localized disease. Here, we utilized single cell RNA-sequencing to characterize the transcriptional landscape of primary Ewing sarcoma tumors and surrounding tumor microenvironment (TME). Copy-number analysis identified subclonal evolution within patients even prior to treatment. Primary tumor samples demonstrate a heterogenous transcriptional landscape with several conserved gene expression programs, including those composed of genes related to proliferation and EWS targets. We also were able to identify the composition of the TME and molecularly dissect the transcriptional profile of circulating tumor cells in peripheral blood at the time of diagnosis.
    Language English
    Publishing date 2024-01-20
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2024.01.18.576251
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Treatment of Kyphosis Arising Secondary to Laminectomy and Irradiation in the Pediatric Population.

    Rogers, Nathan / Selberg, Courtney / LaMotta, Cara / Beebe, Corey / Bloch, Nikki / Erickson, Mark / Donaldson, Nathan J

    Orthopedics

    2021  Volume 44, Issue 4, Page(s) e563–e569

    Abstract: The effects of radiation therapy and laminectomy on the growing spine have been well documented. Due to compromised bone quality after irradiation, spinal fusion has a high failure rate. The aim of this study was to evaluate treatment of post-laminectomy ...

    Abstract The effects of radiation therapy and laminectomy on the growing spine have been well documented. Due to compromised bone quality after irradiation, spinal fusion has a high failure rate. The aim of this study was to evaluate treatment of post-laminectomy and post-irradiation kyphosis in children using a vascularized rib graft (VRG) to augment anterior spinal fusion and posterior spinal fusion. Data were collected retrospectively from electronic medical records for all patients treated at a single institution for post-laminectomy and post-irradiation kyphosis who underwent VRG to augment spinal fusions done between December 2003 and August 2015. Five patients were included in the analysis. Imaging studies were analyzed by 2 senior pediatric orthopedic surgeons and a pediatric orthopedic surgery fellow. The outcome for all 5 patients who underwent VRG were considered successful at most recent clinical follow-up. Success was defined as the following: complete fusion evident through computed tomography scan, no implant failure, and no kyphosis progression. Follow-up ranged from 21 to 63 months. One patient experienced 2 complications: esophageal tear and deep infection. Spinal fusion with a VRG is a viable treatment option for children who have developed kyphosis following laminectomy and irradiation. On long-term follow-up, there has been no evidence of progression of kyphosis for patients who were treated with VRG in either the primary fusion procedure or in subsequent revision procedures. A VRG provides a non-irradiated, vascularized bone graft to bridge the irradiated segments, increasing the stability of the spine. [
    MeSH term(s) Humans ; Kyphosis/diagnostic imaging ; Kyphosis/etiology ; Kyphosis/surgery ; Laminectomy/adverse effects ; Retrospective Studies ; Spinal Fusion/adverse effects ; Spine/surgery ; Treatment Outcome
    Language English
    Publishing date 2021-07-01
    Publishing country United States
    Document type Journal Article
    ZDB-ID 424447-3
    ISSN 1938-2367 ; 0147-7447
    ISSN (online) 1938-2367
    ISSN 0147-7447
    DOI 10.3928/01477447-20210618-18
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Osteosarcoma in an Adolescent with Kniest Dysplasia: A Case Report.

    Tetreault, Allison / Ramalingam, Wendy / Black, Jennifer / Miller, Nancy H / Donaldson, Nathan

    JBJS case connector

    2018  Volume 8, Issue 4, Page(s) e78

    Abstract: Case: A 19-year-old adolescent with Kniest dysplasia was incidentally found to have osteosarcoma of the proximal aspect of the humerus after having a chest radiograph for evaluation of an upper respiratory infection. He underwent chemotherapy and ... ...

    Abstract Case: A 19-year-old adolescent with Kniest dysplasia was incidentally found to have osteosarcoma of the proximal aspect of the humerus after having a chest radiograph for evaluation of an upper respiratory infection. He underwent chemotherapy and resection of the tumor, and there was no evidence of metastasis at the 16-month follow-up.
    Conclusion: Patients with osteochondrodysplasias often have multiple orthopaedic symptoms. Changes in chronic pain symptoms should be investigated to rule out insidious secondary causes of musculoskeletal pain, such as osteosarcoma.
    MeSH term(s) Bone Neoplasms/diagnostic imaging ; Bone Neoplasms/pathology ; Bone Neoplasms/therapy ; Cleft Palate/complications ; Collagen Diseases/complications ; Dwarfism/complications ; Face/abnormalities ; Humans ; Humerus/pathology ; Humerus/surgery ; Hyaline Membrane Disease/complications ; Incidental Findings ; Male ; Osteochondrodysplasias/complications ; Osteosarcoma/diagnostic imaging ; Osteosarcoma/pathology ; Osteosarcoma/therapy ; Radiography, Thoracic ; Young Adult
    Language English
    Publishing date 2018-10-11
    Publishing country United States
    Document type Case Reports ; Journal Article
    ISSN 2160-3251
    ISSN (online) 2160-3251
    DOI 10.2106/JBJS.CC.18.00047
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Congenital Pseudarthrosis of the Tibia.

    O'Donnell, Courtney / Foster, James / Mooney, Ryan / Beebe, Corey / Donaldson, Nathan / Heare, Travis

    JBJS reviews

    2017  Volume 5, Issue 4, Page(s) e3

    Language English
    Publishing date 2017-04-11
    Publishing country United States
    Document type Journal Article
    ISSN 2329-9185
    ISSN (online) 2329-9185
    DOI 10.2106/JBJS.RVW.16.00068
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Does an Algorithmic Approach to Using Brachytherapy and External Beam Radiation Result in Good Function, Local Control Rates, and Low Morbidity in Patients With Extremity Soft Tissue Sarcoma?

    Klein, Jason / Ghasem, Alex / Huntley, Samuel / Donaldson, Nathan / Keisch, Martin / Conway, Sheila

    Clinical orthopaedics and related research

    2017  Volume 476, Issue 3, Page(s) 634–644

    Abstract: Background: High-dose-rate brachytherapy (HDR-BT) and external-beam radiation therapy (EBRT) are two modalities used in the treatment of soft tissue sarcoma. Previous work at our institution showed early complications and outcomes for patients treated ... ...

    Abstract Background: High-dose-rate brachytherapy (HDR-BT) and external-beam radiation therapy (EBRT) are two modalities used in the treatment of soft tissue sarcoma. Previous work at our institution showed early complications and outcomes for patients treated with HDR-BT, EBRT, or a combination of both radiation therapy modalities. As the general indications for each of these approaches to radiation therapy differ, it is important to evaluate the use of each in an algorithmic way, reflecting how they are used in contemporary practice at sites that use these treatments. QUESTION/PURPOSES: (1) To determine the proportions of intermediate- and long-term complications associated with the use of brachytherapy in the treatment of primary high-grade extremity soft tissue sarcomas; (2), to characterize the long-term morbidity of the three radiation treatment groups using the Radiation Therapy Oncology Group/ European Organization for Research and Treatment of Cancer (RTOG/EORTC) Late Radiation Morbidity Scoring Scheme; (3) to determine whether treatment with HDR-BT, EBRT, and HDR-BT+EBRT therapy, in combination with limb-salvage surgery, results in acceptable local control in this high-risk group of sarcomas.
    Methods: We retrospectively studied data from 171 patients with a diagnosis of high-grade extremity soft tissue sarcoma treated with limb-sparing surgery and radiation therapy between 1990 and 2012 at our institution, with a mean followup of 72 months. Of the 171 patients, 33 (20%) were treated with HDR-BT, 128 (75%) with EBRT, and 10 (6%) with HDR-BT+EBRT. We excluded 265 patients with soft tissue sarcomas owing to axial tumor location, previous radiation to the affected extremity, incomplete patient records, patients receiving primary amputation, recurrent tumors, pediatric patients, low- and intermediate-grade tumors, and rhabdoid histology. Fifteen patients (9%) were lost to followup for any reason including died of disease or other causes during the first 12 months postoperatively. This included four patients who received HDR-BT (12%), 11 who received EBRT (9%), and none who received HDR-BT+EBRT (0%) with less than 12 months followup. Determination of radiation therapy technique for each patient was individualized in a multidisciplinary forum of sarcoma specialists. Anticipated close or positive surgical margins and a low likelihood of complex soft tissue procedures were factors that encouraged use of brachytherapy, whereas the anticipated need for secondary procedures and/or soft tissue coverage encouraged use of EBRT alone. Combination therapy was used when the treatment volume exceeded the treatment field of the brachytherapy catheters or when the catheters were used to boost a close or positive surgical margin. Local recurrence, complications, and morbidity outcomes scores (RTOG) were calculated based on chart review. Between-group comparisons pertaining to the proportion of patients experiencing complications, morbidity outcomes scores, and local recurrence rates were not performed because of dissimilarities among the patients in each group at baseline.
    Results: The HDR-BT treatment group showed a high incidence of intermediate-term complications, with the three most common being: deep infection (33%, 11 of 33); dehiscence and delayed wound healing (24%, eight of 33); and seroma and hematoma (21%, seven of 33). The EBRT group showed a high incidence of intermediate- and long-term complications with the three most common being: chronic radiation dermatitis (35%, 45 of 128); fibrosis (27%, 35 of 128); and chronic pain and neuritis (13%, 16 of 128). The RTOG scores for each treatment group were: HDR-BT 0.8 ± SD 1.2; EBRT 1.9 ± 2.0; and HDR-BT+EBRT 1.7 ± 1.7. Overall, 142 of 169 (84%) patients were free from local recurrence: 27 (82%) in the HDR-BT group, 108 (86%) in the EBRT group, and seven (70%) in the combination therapy group.
    Conclusions: In this single-institution study, an algorithmic approach to using HDR-BT and EBRT in the treatment of patients with high-grade soft tissue sarcomas can yield acceptable complication rates, good morbidity outcome scores, and a high degree of local control. Based on these results, we believe HDR-BT is best for patients with an anticipated close margin, a positive surgical margin, and for patients who are unlikely to receive a complex soft tissue procedure. Conversely, if a secondary procedure and/or soft tissue coverage are likely to be used, EBRT alone may be reasonable. Finally, combination therapy might be considered when the treatment volume exceeded the treatment field capacity for HDR-BT or when the catheters were used to boost a close or positive surgical margin.
    Level of evidence: Level IV, therapeutic study.
    MeSH term(s) Adult ; Aged ; Brachytherapy/adverse effects ; Brachytherapy/methods ; Clinical Decision-Making ; Decision Support Techniques ; Female ; Humans ; Limb Salvage ; Male ; Margins of Excision ; Middle Aged ; Neoplasm Grading ; Neoplasm Recurrence, Local ; Predictive Value of Tests ; Radiation Dosage ; Radiotherapy, Adjuvant ; Retrospective Studies ; Risk Assessment ; Risk Factors ; Sarcoma/pathology ; Sarcoma/radiotherapy ; Sarcoma/surgery ; Soft Tissue Neoplasms/pathology ; Soft Tissue Neoplasms/radiotherapy ; Soft Tissue Neoplasms/surgery ; Surgical Wound Dehiscence ; Surgical Wound Infection/etiology ; Time Factors ; Treatment Outcome ; Wound Healing/radiation effects
    Language English
    Publishing date 2017-11-22
    Publishing country United States
    Document type Comparative Study ; Journal Article
    ZDB-ID 80301-7
    ISSN 1528-1132 ; 0009-921X
    ISSN (online) 1528-1132
    ISSN 0009-921X
    DOI 10.1007/s11999.0000000000000079
    Database MEDical Literature Analysis and Retrieval System OnLINE

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