PO-04 REBOUND WEIGHT GAIN AND BLOOD PRESSURE CONTROL AFTER LIVING KIDNEY DONATION AND KIDNEY TRANSPLANTATION

2016 ◽  
Vol 16 (C) ◽  
pp. 90
Author(s):  
Ekamol Tantisattamo ◽  
Weera Sukhumthammarat ◽  
Prapaipan Putthapiban ◽  
Wasawat Vutthikraivit ◽  
Siwadon Pitukweerakul
2019 ◽  
Author(s):  
John McGillicuddy ◽  
Jessica Chandler ◽  
Luke Sox ◽  
Martina Mueller ◽  
Lynne Nemeth ◽  
...  

BACKGROUND Kidney transplant recipients’ poor medication adherence and poor control of comorbidities, particularly hypertension, are risk factors for graft rejection, graft loss, and death. Few randomized controlled trials (RCTs) have been successful in improving sustained medication adherence and blood pressure control among kidney transplantation recipients. We provide rationale for an RCT evaluating a mobile health medical self-management system for kidney transplantation recipients called Smartphone Medication Adherence Saves Kidneys (SMASK). OBJECTIVE Our objective is to determine whether SMASK is efficacious in improving medication adherence and sustaining blood pressure control among kidney transplantation recipients with uncontrolled hypertension and poor medication adherence compared to an enhanced standard care. METHODS This two-arm, 6-month, phase II single-site efficacy RCT will involve 80 kidney transplantation recipients. Participants will be randomly assigned to the SMASK intervention arm or control arm. SMASK includes multilevel components: automated reminders from an electronic medication tray; tailored text messages and motivational feedback, guided by the self-determination theory; and automated summary reports for providers. Evaluations will be conducted preintervention, at 3 and 6 months, and posttrial at 12 months. Specific aims are to test the hypotheses that compared to standard care, the SMASK cohort will demonstrate significantly improved changes at 3, 6, and 12 months in the primary outcome variables medication adherence (proportion with electronic monitor-derived score >0.90) and blood pressure control (proportion meeting and sustaining adherence to the Kidney Disease Improving Global Outcomes [KDIGO] guidelines for blood pressure control); the secondary outcome variables provider adherence to KDIGO guidelines, measured by timing of medication changes and changes in self-determination theory constructs; and the exploratory outcome variables estimated glomerular filtration rate, variability in calcineurin inhibitor trough levels, and proportion of patients meeting and sustaining the 24-hour ambulatory blood pressure below 130/80 mm Hg. After the 6-month evaluation, interviews with a random sample of SMASK subjects (n=20) and health care providers (n=3-5) will assess user reactions including acceptability, usability, and aids/barriers to sustainability. Data from the RCT and interviews will be triangulated to further refine and optimize SMASK and prepare for a multisite effectiveness RCT. RESULTS The SMASK project received funding from National Institute of Diabetes and Digestive and Kidney Diseases in June 2016, obtained institutional review board approval in April 2016, and began data collection in July 2016. As of July 2018, we completed enrollment with a total of 80 participants. CONCLUSIONS This study will provide data regarding the efficacy of SMASK to improve medication adherence and blood pressure control in a cohort of hypertensive kidney transplant recipients. An efficacious SMASK intervention will pave the way for a larger, multicenter, effectiveness RCT powered sufficiently to evaluate clinical events in a real-world setting and with the potential to demonstrate improved outcomes at lower cost than standard care. INTERNATIONAL REGISTERED REPOR DERR1-10.2196/13351


2004 ◽  
Vol 18 (12) ◽  
pp. 871-877 ◽  
Author(s):  
N C Premasathian ◽  
R Muehrer ◽  
P C Brazy ◽  
J D Pirsch ◽  
B N Becker

Nephron ◽  
2018 ◽  
Vol 141 (2) ◽  
pp. 87-97 ◽  
Author(s):  
Mohamed Shantier ◽  
William P. Martin ◽  
Rajneet Singh ◽  
Paul McDermott ◽  
Rory Gallen ◽  
...  

2017 ◽  
Vol 30 (10) ◽  
pp. 1039-1046 ◽  
Author(s):  
Gilad Hamdani ◽  
Edward J Nehus ◽  
Coral D Hanevold ◽  
Judith S VanSickle ◽  
David K Hooper ◽  
...  

2008 ◽  
Vol 29 (2) ◽  
pp. 281-292 ◽  
Author(s):  
Mark W. Vander Weg ◽  
Robert C. Klesges ◽  
Jon O. Ebbert ◽  
Ellen J. Lichty ◽  
Margaret DeBon ◽  
...  

2020 ◽  
Author(s):  
Ali M Shendi ◽  
Andrew Davenport

Abstract Background The choice of dialysate sodium (DNa) for haemodialysis (HD) patients remains controversial, with some studies reporting that a lower DNa improves blood pressure control and reduces intradialytic weight gain. Studies on DNa depend on the alignment of programmed to delivered DNa. We wished to determine whether there were differences between programmed and delivered DNa. Methods Dialysate samples were obtained from three dialysis machines: Fresenius 4008H (F4008H) and 5008S (F5008S) and B-Braun hemodiafiltration (HDF) Dialog+(BB). DNa was measured by indirect ion-selective electrode (ISE), flame photometry (FP) and ion chromatography (IC) at different DNa concentrations. Results We tested 18 F5008S, 18 F4008H and 31 BB machines over 153 HD treatments. The median measured minus programmed DNa was significantly greater with the BB machine [ISE, 7 (6–8); FP, 7 (6–8); IC, 6 (5–7)], followed by the F4008H [ISE, 5.5 (5–7); FP, 4 (2.25–5.75); IC, 4 (2–5)]and F5008S [ISE, 4 (2–5); FP, 1 (−1–1.75); IC, 1 (−0.5 to 2)] mEq/L (P < 0.05). At higher programmed DNa (140–145 mEq/L), measured DNa was greater for the BB and F4008 machines by all methods (P < 0.05), but only by ISE for the F5008 (P < 0.05). Conclusions We noted a systematic bias in DNa delivery with measured DNa being greater than that programmed by our HD machines. The magnitude of the bias varied between machines and with DNa. Our results may help explain the diverse results reported in studies of DNa.


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