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Sponsor: AstraZeneca
Conditions: Hyperkalaemia
Countries: China
The study is a multi-center prospective (primary data) non-interventional cohort study which enrolls 1500 patients including new and ongoing users on SZC at Study Enrollment Day in real-world clinical practice. The eligible study patients will be identified by physicians in each study site by assessing the patients or reviewing the medical record. The prescription (including initiation, dose-adjusting or interruption) or discontinuation of SZC will be determined by physicians as per real-world clinical practice and in accordance with the local label. Any AZ employee, or member of the research operation team must not intervene in the decision-making of any physician or patient through any approach, at any time during the study. Every patient will be followed up according to standard clinical practice for 6 months from enrolment.
Sex: ALL
Age: 18 Years to —
Healthy volunteers: No
Study type: OBSERVATIONAL
Inclusion Criteria: * Age ≥ 18 year-old * Provision of patient informed consent prior to any study procedure * HK (sK+ \> 5.0 mmol/L) diagnosed by physicians within 1 year before Study Enrolment Day * Currently taking SZC, or has been prescribed and agree to start taking SZC since Study Enrolment Day. Exclusion Criteria: * Being unable to comply with study-specified procedures * Has ever participated in current study before, or participating in any interventional study at Study Enrolment Day or within the last 3 months before Study Enrolment Day
- Anshan, China
- Beijing, China
- Benxi, China
- Changsha, China
- Changshu, China
- Chengdu, China
- Dalian, China
- Guangzhou, China
- Handan, China
- Hangzhou, China
- Hefei, China
- Hohhot, China
- Jiaxing, China
- Kunshan, China
- Linfen, China
- Nanjing, China
- Nanyang, China
- Ningbo, China
- Qidong, China
- Shijiazhuang, China
- Shiyan, China
- Taian, China
- Taishing, China
- Tianjin, China
- Wenzhou, China
- Xi'an, China
- Xinghua, China