Background: Single-needle (SN) dialysis has been accepted as one of the alternative modes of renal replacement therapy. Despite its advantages it is not widely practiced due to the belief of underdialysis by this technique. However, it is used routinely in many hemodialysis units. We therefore aimed to study the efficacy and determine parameters that reflect the dialysis efficiency. The complications and adverse events were also evaluated. The times required to achieve maximal adequacy of dialysis were compared between 4-, 4.5-and 5.0-hour dialysis sessions.
Methods: Ten stable end-stage renal disease patients who regularly used the standard hemodialysis technique with double-needle (DN) dialysis were switched to SN dialysis for three consecutive dialysis session times (4, 4.5 and 5.0 h, respectively) for 3 weeks in each period. The following parameters including Kt/V, percent recirculation, calcium, phosphorus, hematocrit, and LDH level were studied at the start and end of each period.
Results: After switching to the SN mode, the Kt/V did not change significantly from the baseline value. However, in the subgroup analysis, only the thrice-weekly group achieved the target Kt/V. Kt/V declined insignificantly in the twice-weekly group but did not reach the recommended level. The other parameters were not different from the DN group. The 4-hour group had a similar Kt/V to the other groups and had less recirculation. There were no major complications during the SN phase. The outcome of the fistulas was excellent.
Conclusion: The thrice-weekly SN hemodialysis with 4-hour session time has the same efficacy as the conventional DN technique with no more adverse events. Therefore, the SN hemodialysis system may be suitable for routine thrice-weekly hemodialysis in the selected group of patients.
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http://dx.doi.org/10.1159/000113008 | DOI Listing |
Background: Maintenance hemodialysis (MHD) is an effective treatment for patients with end-stage renal disease. Although MHD can prolong the survival of patients, their quality of life is lower and the fatality rate is higher. This work analyzed the factors related to the autogenous arteriovenous fistula (AVF)-like expansion of non-diabetic MHD patients by vascular ultrasound (VUS).
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Department of Obstetrics and Gynecology, University of Oklahoma Tulsa, OU-TU School of Community Medicine, Tulsa, OK.
Objective: The purpose of this review was to examine new evidence since our 2019 guidelines for cervical cancer (CC) screening in non-HIV immunocompromised persons and to provide updated recommendations based on literature review and expert opinion. In addition, human papillomavirus (HPV) vaccine efficacy in these populations was reviewed.
Methods: A literature search was performed similar to our previous publication but was conducted through March 2023.
Sleep
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Santa Barbara Actuaries Inc., Santa Barbara, CA, USA.
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Kidney Med
January 2025
Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Expansion of home hemodialysis (HHD) provides an opportunity to improve clinical outcomes, reduce cost of care, and address the staffing challenges currently faced in caring for patients with kidney failure on replacement therapy. To increase HHD expansion, current practices and barriers to home dialysis must be examined and addressed. One such barrier is vascular access for HHD; although tunneled hemodialysis central venous catheters (CVCs) have been used for decades, physicians still hesitate to send patients home without a mature, functional arteriovenous access.
View Article and Find Full Text PDFClin Kidney J
January 2025
State Key Laboratory of Reproductive Medicine and Offspring Health, Center for Reproductive Medicine, Institute of Women, Children and Reproductive Health, Shandong University, Jinan, Shandong, China.
Background: Hereditary nephropathy is an important cause of renal insufficiency and end-stage renal disease. Therefore, for couples with monogenic nephropathy, preventing transmission of the disease to offspring is urgent. Preimplantation genetic testing for monogenic disorders (PGT-M) is a means to prevent intergenerational inheritance by screening and transplanting normal embryos.
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