Introduction: Chronic kidney disease (CKD) is associated with multimorbidity and high treatment burden. Pill-burden is one component of the overall treatment burden. However, little is known about its magni-tude and contribution to the overall treatment burden among patients with advanced stages of CKD. This study aimed to quantify the magnitude of pill-burden in dialysis-dependent vs. non-dialysis-dependent advanced-stage CKD patients and its association with treatment burden. Methods: This was a cross-sectional study for the assessment of pill-burden and treatment burden among non-dialysis and hemodialysis (HD)-dependent CKD patients. Pill-burden was quantified as "number of pills/patient/week" through electronic medical record, while treatment burden was assessed using the "Treatment Burden Questionnaire (TBQ)". Furthermore, oral and parenteral medication burden was also quantified. Data were analyzed using both descriptive and inferential analysis, including Mann - Whitney U test and two-way between groups analysis of variance (ANOVA). Results: Among the 280 patients included in the analysis, the median (IQR) number of prescribed chronic medications was 12 (5.7) oral and 3 (2) parenteral medications. The median (IQR) pill-burden was 112 (55) pills/week. HD patients experienced higher pill-burden than non-dialysis patients [122 (61) vs. 109 (33) pills/week]; however, this difference did not reach statistical significance (p = 0.81). The most commonly prescribed oral medications were vitamin D (90.4%), sevelamer carbonate (65%), cinacalcet (67.5%), and statins (67.1%). Overall, patients who had high pill-burden (>= 112 pills/week) had signifi-cantly higher perceived treatment burden compared to low pill-burden patients (<112 pills/week) [47 (36.2) vs. 38.5(36.7); p = 0.0085]. However, two-way ANOVA showed that dialysis status is the significant contributor to the treatment-burden in the high overall pill-burden group (p < 0.01), the high oral-medication-burden group (p < 0.01), and the high parenteral-medication-burden group (p = 0.004). Conclusions: Patients with advanced CKD experienced a high pill-burden, which increases the treatment burden; however, the dialysis status of the patient is the main factor affecting the overall treatment bur -den. Future intervention studies should target this population with an aim to reduce polypharmacy, pill-burden, and treatment burden, which may ultimately improve CKD patients' quality of life.(c) 2023 The Author(s). Published by Elsevier B.V. on behalf of King Saud University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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Vet Adm Boston Healthcare Syst, Vet Adm Cooperat Studies Program, Massachusetts Vet Epidemiol Res & Informat Ctr, Boston, MA 02130 USA
Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USAVet Adm Boston Healthcare Syst, Vet Adm Cooperat Studies Program, Massachusetts Vet Epidemiol Res & Informat Ctr, Boston, MA 02130 USA
Lawer, Elizabeth V.
Bradbury, Brian D.
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Amgen Inc, Dept Biostat & Epidemiol, Thousand Oaks, CA 91320 USAVet Adm Boston Healthcare Syst, Vet Adm Cooperat Studies Program, Massachusetts Vet Epidemiol Res & Informat Ctr, Boston, MA 02130 USA
Bradbury, Brian D.
Fonda, Jennifer R.
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Vet Adm Boston Healthcare Syst, Vet Adm Cooperat Studies Program, Massachusetts Vet Epidemiol Res & Informat Ctr, Boston, MA 02130 USAVet Adm Boston Healthcare Syst, Vet Adm Cooperat Studies Program, Massachusetts Vet Epidemiol Res & Informat Ctr, Boston, MA 02130 USA
Fonda, Jennifer R.
Gaziano, J. Michael
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Vet Adm Boston Healthcare Syst, Vet Adm Cooperat Studies Program, Massachusetts Vet Epidemiol Res & Informat Ctr, Boston, MA 02130 USA
Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USAVet Adm Boston Healthcare Syst, Vet Adm Cooperat Studies Program, Massachusetts Vet Epidemiol Res & Informat Ctr, Boston, MA 02130 USA
Gaziano, J. Michael
Gagnon, David R.
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Gagnon, David R.
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY,
2010,
5
(04):
: 667
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672
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UK Renal Registry, Brandon House Bldg 20A1,Southmead Rd, Bristol BS34 7RR, Avon, EnglandUK Renal Registry, Brandon House Bldg 20A1,Southmead Rd, Bristol BS34 7RR, Avon, England
Santhakumaran, Shalini
van der Veer, Sabine N.
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Univ Manchester, Manchester Acad Hlth Sci Ctr, Ctr Hlth Informat, Div Informat Imaging & Data Sci, Manchester, Lancs, EnglandUK Renal Registry, Brandon House Bldg 20A1,Southmead Rd, Bristol BS34 7RR, Avon, England
van der Veer, Sabine N.
Thomas, Nicola
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London South Bank Univ, Sch Hlth & Social Care, London, EnglandUK Renal Registry, Brandon House Bldg 20A1,Southmead Rd, Bristol BS34 7RR, Avon, England
Thomas, Nicola
Gair, Rachel
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UK Renal Registry, Brandon House Bldg 20A1,Southmead Rd, Bristol BS34 7RR, Avon, EnglandUK Renal Registry, Brandon House Bldg 20A1,Southmead Rd, Bristol BS34 7RR, Avon, England
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Rutgers Robert Wood Johnson Med Sch, Gastroenterol & Hepatol, New Brunswick, NJ USARutgers Robert Wood Johnson Med Sch, Gastroenterol & Hepatol, New Brunswick, NJ USA
Elsaid, Mohamed I.
Pentakota, Sri Ram
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Pentakota, Sri Ram
Li, You
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Rutgers Robert Wood Johnson Med Sch, Gastroenterol & Hepatol, New Brunswick, NJ USARutgers Robert Wood Johnson Med Sch, Gastroenterol & Hepatol, New Brunswick, NJ USA
Li, You
John, Tina
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Rutgers Robert Wood Johnson Med Sch, Gastroenterol & Hepatol, New Brunswick, NJ USARutgers Robert Wood Johnson Med Sch, Gastroenterol & Hepatol, New Brunswick, NJ USA
John, Tina
Rustgi, Vinod K.
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