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1.
Hum Immunol ; 84(4): 278-285, 2023 Apr.
Article in English | MEDLINE | ID: mdl-36868898

ABSTRACT

Although rare, infection and vaccination can result in antibodies to human leukocyte antigens (HLA). We analyzed the effect of SARS-CoV-2 infection or vaccination on HLA antibodies in waitlisted renal transplant candidates. Specificities were collected and adjudicated if the calculated panel reactive antibodies (cPRA) changed after exposure. Of 409 patients, 285 (69.7 %) had an initial cPRA of 0 %, and 56 (13.7 %) had an initial cPRA > 80 %. The cPRA changed in 26 patients (6.4 %), 16 (3.9 %) increased, and 10 (2.4 %) decreased. Based on cPRA adjudication, cPRA differences generally resulted from a small number of specificities with subtle fluctuations around the borderline of the participating centers' cutoff for unacceptable antigen listing. All five COVID recovered patients with an increased cPRA were female (p = 0.02). In summary, exposure to this virus or vaccine does not increase HLA antibody specificities and their MFI in approximately 99 % of cases and 97 % of sensitized patients. These results have implications for virtual crossmatching at the time of organ offer after SARS-CoV-2 infection or vaccination, and these events of unclear clinical significance should not influence vaccination programs.


Subject(s)
COVID-19 , Kidney Transplantation , Humans , Female , Male , Tissue Donors , Histocompatibility Testing/methods , Kidney Transplantation/methods , SARS-CoV-2 , Antibodies , HLA Antigens , Vaccination , Isoantibodies
2.
Am Surg ; 88(8): 2017-2023, 2022 Aug.
Article in English | MEDLINE | ID: mdl-34049446

ABSTRACT

OBJECTIVE: The COVID-19 pandemic has had a significant impact on patient care, including the increased utilization of contact-free clinic visits using telemedicine. We looked to assess current utilization of, experience with, and opinions regarding telemedicine by general surgery residents at an academic university-based surgical training program. DESIGN: A response-anonymous 19-question survey was electronically distributed to all general surgery residents at a single academic university-based general surgery residency program. SETTING: University of Southern California (USC) general surgery residency participants: Voluntarily participating general surgery residents at the University of Southern California. RESULTS: The response rate from USC general surgery residents was 100%. A majority of residents (76%) had utilized either video- or telephone-based visits during their careers. No resident had undergone formal training to provide telemedicine, although most residents indicated a desire for training (57.1%) and acknowledged that telemedicine should be a part of surgical training (75.6%). A wide variety of opinions regarding the educational experience of residents participating in telemedicine visits was elicited. CONCLUSIONS: The COVID-19 pandemic brought telemedicine to the forefront as an integral part of future patient care, including for surgical patients. Additional investigations into nationwide telemedicine exposure and practice among United States general surgery residencies is imperative, and the impact of the implementation of telemedicine curricula on general surgery resident telemedicine utilization, comfort with telemedicine technology, and patient outcomes are further warranted. COMPETENCIES: Practice-based learning, systems-based practice, interpersonal and communication skills.


Subject(s)
COVID-19 , General Surgery , Internship and Residency , Telemedicine , COVID-19/epidemiology , Education, Medical, Graduate , General Surgery/education , Humans , Pandemics , Patient Care , United States
3.
Ann Surg ; 274(4): 613-620, 2021 10 01.
Article in English | MEDLINE | ID: mdl-34506316

ABSTRACT

OBJECTIVE: To investigate the optimal timing of direct acting antiviral (DAA) administration in patients with hepatitis C-associated hepatocellular carcinoma (HCC) undergoing liver transplantation (LT). SUMMARY OF BACKGROUND DATA: In patients with hepatitis C (HCV) associated HCC undergoing LT, the optimal timing of direct-acting antivirals (DAA) administration to achieve sustained virologic response (SVR) and improved oncologic outcomes remains a topic of much debate. METHODS: The United States HCC LT Consortium (2015-2019) was reviewed for patients with primary HCV-associated HCC who underwent LT and received DAA therapy at 20 institutions. Primary outcomes were SVR and HCC recurrence-free survival (RFS). RESULTS: Of 857 patients, 725 were within Milan criteria. SVR was associated with improved 5-year RFS (92% vs 77%, P < 0.01). Patients who received DAAs pre-LT, 0-3 months post-LT, and ≥3 months post-LT had SVR rates of 91%, 92%, and 82%, and 5-year RFS of 93%, 94%, and 87%, respectively. Among 427 HCV treatment-naïve patients (no previous interferon therapy), patients who achieved SVR with DAAs had improved 5-year RFS (93% vs 76%, P < 0.01). Patients who received DAAs pre-LT, 0-3 months post-LT, and ≥3 months post-LT had SVR rates of 91%, 93%, and 78% (P < 0.01) and 5-year RFS of 93%, 100%, and 83% (P = 0.01). CONCLUSIONS: The optimal timing of DAA therapy appears to be 0 to 3 months after LT for HCV-associated HCC, given increased rates of SVR and improved RFS. Delayed administration after transplant should be avoided. A prospective randomized controlled trial is warranted to validate these results.


Subject(s)
Antiviral Agents/administration & dosage , Carcinoma, Hepatocellular/surgery , Hepatitis C, Chronic/drug therapy , Liver Neoplasms/surgery , Liver Transplantation , Aged , Benzimidazoles/administration & dosage , Carbamates/administration & dosage , Carcinoma, Hepatocellular/virology , Drug Administration Schedule , Drug Combinations , Female , Fluorenes/administration & dosage , Hepatitis C, Chronic/complications , Heterocyclic Compounds, 4 or More Rings/administration & dosage , Humans , Liver Neoplasms/virology , Male , Middle Aged , Pyrrolidines/administration & dosage , Quinoxalines/administration & dosage , Retrospective Studies , Sofosbuvir/administration & dosage , Sulfonamides/administration & dosage , Sustained Virologic Response
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