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Pilot Study for the Tight K Study

PILOT STUDY for the Tight K TRIAL. Arrhythmias on the Cardiac Intensive Care Unit - Does Maintenance of High-normal Serum Potassium Levels Matter?

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03195647
Acronym
TightK
Enrollment
160
Registered
2017-06-22
Start date
2017-08-01
Completion date
2018-05-29
Last updated
2020-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Arrythmias

Keywords

cardiovascular, potassium supplementation, coronary artery by pass surgery

Brief summary

The primary purpose of this pilot study will be feasibility of recruitment. However, in order to further inform a full randomised controlled trial (RCT), information on the incidence of atrial fibrillation (AF) and other arrhythmias, hospital length of stay, resource use and morbidity will be collected.

Detailed description

Arrhythmias are common in critical care, with atrial tachyarrhythmias (and especially AF) being the most prevalent. This is especially true after cardiac surgery, with approximately 1 in 3 patients affected. The occurrence of new-onset post-operative AF is associated with increased short and long-term mortality, intensive care unit (ICU) and hospital stay and costs of care. This association appears causal, even after correction for confounding factors. Potassium (K+) plays an important role in cardiac electrophysiology and abnormal levels may cause arrhythmias. Hypokalaemia, defined as a serum K+ \<3.6 milliequivalents per litre (mEq/L) is thus associated with an increased incidence of ventricular arrhythmia after myocardial infarction. Low K+ levels are common following cardiac surgery, and appear marginally lower in those suffering atrial arrhythmias in this context. Despite an absence of proof that this association is causal, efforts to maintain serum \[K+\] in the 'high-normal' range (4.5 - 5.5 mEq/L) are considered 'routine practice' for AF prevention worldwide. The efficacy of such intervention remains unproven and data supporting this practice is extremely limited, being derived from observational rather than interventional studies. Indeed, no data exist to demonstrate that maintaining a high-normal potassium level is beneficial, or that aggressive replenishment of potassium in patients with heart disease necessarily leads to a better clinical outcome. Furthermore, the method of potassium supplementation may be problematic. Oral replacement is not possible immediately post-operatively. Central venous administration is thus generally utilised in the early post-operative period. However, this practice is both time-consuming and costly: the intravenous administration of potassium carries recognised clinical risk, and is now prescribed in pre-diluted doses, stored securely for a safety purposes. Oral replacement is commonly associated with profound nausea, and is very poorly tolerated by patients. The investigators have estimated that the annual spending on potassium in cardiothoracic patients at Barts Health National Health Service (NHS) Trust is £100,000, compared to £16,500 for Milrinone (perceived as a high cost drug (2011-2012 prices). Additional costs relating to nursing time, drug checks, and intravenous connection and charting are also accrued. Central venous catheters may also be routinely left in situ solely for the purposes of parenteral potassium replacement; leading to an increased risk of line-related sepsis. The routine maintenance of serum K+ in the high-normal range is thus a costly and unproven practice.

Interventions

The trial treatment will start when patients are admitted to the intensive care unit after their surgery. The patient will undergo regular blood investigations, as per current practice. The frequency of K+ monitoring while on ICU will be according to clinician / nursing staff preference. Potassium supplementation will be according to local hospital protocols. This can be either via an intravenous infusion or as a tablet. Patients will otherwise be treated as per current hospital protocol.

Sponsors

London School of Hygiene and Tropical Medicine
CollaboratorOTHER
Barts & The London NHS Trust
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1\. All patients undergoing isolated elective coronary artery bypass graft (CABG)

Exclusion criteria

1. Age less than 18 years 2. Previous AF 3. Concurrent patient involvement in another clinical study assessing post-operative interventions 4. On-going infection/sepsis at the time of operation 5. Pre-op high-degree atrioventricular (AV) block 6. Pre-op serum K+ greater than 5.5 mEq/L 7. Current or previous use of medication for the purposes of cardiac rhythm management 8. Dialysis dependent end stage renal failure

Design outcomes

Primary

MeasureTime frameDescription
Total number of patients recruited over a 6 month period6 monthsThe pilot study is being conducted to assess if it is feasible to recruit the required patient population into the study. The aim of the pilot is to recruit 160 patients over 6 months from two different centres.
Number of patients successfully randomised into the study to receive standard either usual care or control of potassium at the lower limit of the normal range6 monthsThe pilot study will investigate if it is feasible to randomised patients between the control and intervention arms of the study
Protocol violation rate6 monthsFeasibility of ensuring that protocol violation rate is no more than 10%
Number of patient with outcome data at 28 days6 monthsThis is a feasibility and one of the main outcome will be to assess the number of participants with outcome data at 28 days. The study will aim to follow up 90% of the patients randomised.

Secondary

MeasureTime frameDescription
Incidence of in-patient mortality28 days from randomisationNumber of patients deceased during their hospital stay
Incidence of new onset atrial fibrillationMaximum of 5 daysEpisode of AF lasting at least 30 seconds that is clinically detected and/or electrocardiographically confirmed post surgery until day 5
Cost-effectiveness28 days from randomisation
Incidence of mortality28 days from randomisationAll incidence of mortality during hospital stay and follow up
Mean critical care length of stayMaximum 28 daysAverage time patients are treated on critical care ward
Mean hospital length of stayMaximum 28 daysAverage time patients are inpatients in all hospital wards
Incidence of all other arrhythmias, defined using standard diagnostic criteriaMaximum of 5 daysAll other arrhythmias detected clinically and/or review of holter monitor data

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026