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1.
World J Urol ; 42(1): 214, 2024 Apr 06.
Article in English | MEDLINE | ID: mdl-38581460

ABSTRACT

PURPOSE: A living donor kidney transplant is the optimal treatment for chronic renal impairment. Our objective is to assess if lean skeletal muscle mass and donor factors such as body mass index, hypertension, and age impact on renal function following donor nephrectomy. METHODS: Potential donors undergo CT angiography as part of their work-up in our institution. Using dedicated software (Horos®), standardized skeletal muscle area measured at the L3 vertebrae was calculated. When corrected for height, skeletal muscle index can be derived. Skeletal muscle mass index below predefined levels was classified as sarcopenic. The correlation of CT-derived skeletal muscle index and postoperative renal function at 12 months was assessed. Co-variables including donor gender, age, body mass index (BMI), and presence of pre-op hypertension were also assessed for their impact on postoperative renal function. RESULTS: 275 patients who underwent living donor nephrectomy over 10 years were included. Baseline pre-donation glomerular filtration rate (GFR) and renal function at one year post-op were similar between genders. 29% (n = 82) of patients met the criteria for CT-derived sarcopenia. Sarcopenic patients were more likely to have a higher GFR at one year post-op (69.3 vs 63.9 mL/min/1.73 m2, p < 0.001). The main factors impacting better renal function at one year were the presence of sarcopenia and younger age at donation. CONCLUSION: When selecting donors, this study highlights that patients with low skeletal mass are unlikely to underperform in terms of recovery of their renal function postoperatively at one year when compared to patients with normal muscle mass and should not be a barrier to kidney donation.


Subject(s)
Hypertension , Kidney Transplantation , Sarcopenia , Humans , Male , Female , Nephrectomy , Sarcopenia/diagnostic imaging , Living Donors , Retrospective Studies , Kidney/physiology , Glomerular Filtration Rate/physiology
2.
Clin Transplant ; 35(1): e14156, 2021 01.
Article in English | MEDLINE | ID: mdl-33222237

ABSTRACT

BACKGROUND: This study aims to evaluate allograft and patient outcomes among recipients of kidney transplants after non-renal solid organ transplants. We also aim to compare our findings with recipients of a repeat kidney transplant. METHODS: We performed an analysis on kidney transplant recipients who underwent kidney transplantation after a non-renal solid organ transplant. Survival data were stratified into 2 groups: Group A (n = 37) consisted of recipients of a kidney transplant after prior non-renal solid organ transplant, and Group B (n = 330) consisted of recipients of a repeat kidney transplant. RESULTS: The 1-,5-, and 10-year graft survival (death-censored) for recipients of a kidney transplant post-non-renal solid organ transplant (Group A) were 97.3%, 91.5%, and 86.9%, compared with 97.9%, 90.2%, and 83.4% for recipients of a repeat kidney transplant (Group B) (p = .32). The 1-, 5-, and 10-year patient survival rates were 97.3%, 82.7%, and 79.1% in Group A compared to 97.9%, 90.2%, and 83.4% in Group B. Unadjusted overall patient survival was significantly lower for Group A (p = .017). CONCLUSION: Kidney transplant recipients who have undergone a previous non-renal solid organ transplant have similar allograft survival outcomes, but higher long-term mortality rates compared to repeat kidney transplant recipients.


Subject(s)
Kidney Transplantation , Organ Transplantation , Graft Survival , Humans , Retrospective Studies , Transplantation, Homologous
3.
Clin Transplant ; 34(8): e13907, 2020 08.
Article in English | MEDLINE | ID: mdl-32416641

ABSTRACT

INTRODUCTION: Few studies investigate significant perioperative predictors for long-term renal allograft survival after second kidney transplant (SKT). We compared long-term survival following SKT with primary kidney transplant and determined predictors of renal allograft failure after SKT. METHODS: Outcomes of all primary or second kidney transplant recipients at a national kidney transplant center between 1993 and 2017 were reviewed. The primary outcomes measurements were renal allograft survival for both first and second kidney transplants. Secondary outcome measurements were incidence of delayed graft function (DGF), incidence of acute rejection (AR), and predictors for renal allograft survival in SKT recipients. RESULTS: In total, there were 392 SKTs and 2748 primary kidney transplants performed between 1993 and 2017. The 1-, 5-, and 10-year death-censored graft survival for deceased-donor recipients was 95.3%, 88.7%, and 78.2% for primary kidney transplant and 94.9%, 87.1%, and 74.9% for SKT (P = .0288). Survival of primary renal allograft <6 years (HR 0.6, P = .017), AR episodes (HR 1.6, P = .031), DGF (HR 2.0, P = .005), and HLA-DR MM (HR 1.7, P = .018) was independent predictors of long-term renal allograft failure after SKT. CONCLUSION: These findings may provide important information on long-term survival outcomes after SKT and for identifying patients at risk for long-term renal allograft failure after SKT.


Subject(s)
Kidney Transplantation , Allografts , Graft Rejection/etiology , Graft Survival , Humans , Kidney , Retrospective Studies , Risk Factors
4.
Exp Clin Transplant ; 18(1): 13-18, 2020 02.
Article in English | MEDLINE | ID: mdl-31266437

ABSTRACT

OBJECTIVES: Delayed graft function after kidney transplant can affect patient and graft survival, resulting in prolonged hospital stay and need for dialysis. Ischemia times during organ procurement and reanastomosis at transplant are key factors in delayed graft function. MATERIALS AND METHODS: We analyzed all living- and deceased-donor renal transplants in Ireland over a 33-month period, with effect of warm ischemia time during anastomosis on delayed graft function being the primary outcome. We performed statistical regression analyses to account for confounding variables. Patients had identical surgical technique and immunosuppression protocols. RESULTS: Of 481 transplants during the study period, 20 patients were excluded because of paired-kidney exchange, nephron dosing transplant, or simul-taneous pancreas-kidney transplant. In the donor pool, 70% were donors after brainstem death, 3.6% were donors after cardiac death, and 26% were living donors. All living donors were direct altruistic donors and underwent stringent assessment via the ethics committee and multidisciplinary team meeting. Of living donors, 8% were not related. These were true altruistic donors who were acquaintances of the recipients and volunteered themselves for assessment. They were assessed in accordance with the declaration of Istanbul and received no compensation of any kind for donation. Of total patients, 18% had delayed graft function, defined as need for dialysis within 7 days of transplant. Warm ischemia time during anastomosis significantly affected risk of delayed graft function but not graft survival or function at 3 months. This factor did not correlate with hospital stay duration. Time on dialysis and recipient weight significantly correlated with risk of delayed graft function. CONCLUSIONS: Our findings support a role for minimizing warm ischemia time during anastomosis to reduce delayed graft function and need for dialysis in the perioperative period. However, a longer time does not appear to affect creatinine levels and therefore graft function at 3 months.


Subject(s)
Delayed Graft Function/etiology , Kidney Failure, Chronic/surgery , Kidney Transplantation/adverse effects , Vascular Surgical Procedures/adverse effects , Warm Ischemia/adverse effects , Adult , Anastomosis, Surgical , Body Weight , Databases, Factual , Delayed Graft Function/diagnosis , Female , Humans , Ireland , Kidney Failure, Chronic/diagnosis , Living Donors , Male , Middle Aged , Renal Dialysis/adverse effects , Risk Assessment , Risk Factors , Time Factors , Treatment Outcome
5.
BMJ Case Rep ; 12(12)2019 Dec 16.
Article in English | MEDLINE | ID: mdl-31848141

ABSTRACT

Duplication of the inferior vena cava (IVC) resulting in an accessory left-sided IVC is a relatively rare vascular anomaly with a reported prevalence of 0.7%. Radiologically, a duplicated left-sided IVC is usually seen as a continuation of the left common iliac vein, crossing anterior to the aorta at the level of the renal vein to join the right-sided IVC. We present a rare case in which an accessory left-sided IVC was discovered intraoperatively, in a 47-year-old living donor, posing significant intraoperative challenges regarding extraction and subsequent transplantation.


Subject(s)
Delayed Graft Function/diagnosis , Intraoperative Complications/diagnosis , Living Donors , Vena Cava, Inferior/abnormalities , Female , Humans , Kidney Transplantation , Male , Middle Aged , Nephrectomy , Recovery of Function
6.
BMJ Case Rep ; 20182018 Feb 11.
Article in English | MEDLINE | ID: mdl-29440239

ABSTRACT

Extranodal follicular dendritic cell sarcoma (FDCS) is a very rare tumour, only reported in case reports and case series. It poses diagnostic and management challenge both to the clinician and pathologist. We present such a rare case of duodenal FDCS in a 56-year-old woman who was recently managed in our institution. Repeated pre surgical biopsies were non-diagnostic and the final diagnosis was made only after surgical excision of the tumour and with the help of histopathological and immunohistochemical studies. The patient had a complete en block resection of the tumour and was discharged home well 5 days postsurgery. To the best of our knowledge, this is the first case of FDCS reported arising from the duodenum.


Subject(s)
Dendritic Cell Sarcoma, Follicular/diagnosis , Duodenal Neoplasms/diagnosis , Duodenum/pathology , Anastomosis, Surgical , Antineoplastic Combined Chemotherapy Protocols , Colectomy , Dendritic Cell Sarcoma, Follicular/therapy , Duodenal Neoplasms/therapy , Female , Humans , Ileum , Immunohistochemistry , Middle Aged , Rare Diseases , Treatment Outcome
7.
Pediatr Surg Int ; 25(7): 651-3, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19517123

ABSTRACT

Colonic atresia, unlike small intestine atresia, is a rare congenital malformation. Congenital absence of the entire colon is exceptionally rare. Moreover, an association of omphalocele and complete absence of the colon has not yet been reported in the literature. We present an infant born with such combination of congenital anomalies.


Subject(s)
Abnormalities, Multiple , Hernia, Umbilical/complications , Hernia, Umbilical/surgery , Intestinal Atresia/complications , Intestine, Large/abnormalities , Deafness/complications , Heart Septal Defects, Atrial/complications , Humans , Infant, Newborn , Male , Parenteral Nutrition, Total , Rare Diseases , Urinary Bladder/abnormalities
8.
BMC Fam Pract ; 9: 6, 2008 Jan 28.
Article in English | MEDLINE | ID: mdl-18226249

ABSTRACT

BACKGROUND: Multimorbidity has been defined as the co-existence of two or more chronic conditions. It has a profound impact on both the individuals affected and on their use of healthcare services. The limited research to date has focused on its epidemiology rather than the development of interventions to improve outcomes in multimorbidity patients, particularly for patients aged less than 65 years. Potential barriers to such research relate to methods of disease recording and coding and examination of the process of care. We aimed to assess the feasibility of identifying younger individuals with multimorbidity at general practice level and to explore the effect of multimorbidity on the type and volume of health care delivered. We also describe the barriers encountered in attempting to carry out this exploratory research. METHODS: Cross sectional survey of GP records in two large urban general practices in Dublin focusing on poorer individuals with at least three chronic conditions and aged between 45 and 64 years. RESULTS: 92 patients with multimorbidity were identified. The median number of conditions was 4 per patient. Individuals received a mean number of 7.5 medications and attended a mean number of GP visits of 11.3 in the 12 months preceding the survey. Barriers to research into multimorbidity at practice level were identified including difficulties relating to GP clinical software; variation in disease coding; assessment of specialist sector activity through the GP-specialist communications and assessment of the full scale of primary care activity in relation to other disciplines and other types of GP contacts such as home visits and telephone contacts. CONCLUSION: This study highlights the importance of multimorbidity in general practice and indicates that it is feasible to identify younger patients with multimorbidity through their GP records. This is a first step towards planning a clinical intervention to improve outcomes for such patients in primary care.


Subject(s)
Chronic Disease/epidemiology , Comorbidity , Family Practice/organization & administration , Health Services Research/methods , Chronic Disease/classification , Female , Humans , International Classification of Diseases , Ireland/epidemiology , Male , Middle Aged , Primary Health Care/statistics & numerical data , Socioeconomic Factors , Urban Health Services
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