Thoracic SurgeryNCT02878733
Albumin Administration and Outcomes in Cardiac Surgery
An observational study of Thoracic Surgery, run by Vanderbilt University.
Trial summary
The invesitgators utilized the Cerner HealthFacts database (a large HIPAA-compliant clinical-administrative database maintained by Cerner Inc., USA) to identify a cohort of 6,249 adults that underwent on-pump cardiac surgery for valve and/or coronary artery procedures between January 2001 and March 2013. Read more about this study
- Who is it for?
- Ages 18 to 85 years
- Conditions the study is for
- Thoracic Surgery
- What is being tested?
- Albumin
- How many people
- 6,249 participants
- Where
- No sites listed yet
- Study dates
- Jan 2012to Mar 2013
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 85 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Adults that underwent isolated valve, isolated CABG or two or more procedures utilizing CPB
Who may be able to join
- Adults that underwent isolated valve, isolated CABG or two or more procedures utilizing CPB
Who cannot join
- death within 24 hours of index procedure
- patients undergoing heart transplantation
- Patients with missing or incomplete admission, procedure, and/or discharge dates, gender, and age were excluded
- patients with any of the following Elixhauser comorbidities: AIDS, lymphoma, metastatic cancer, solid tumors without metastases
About this study
Official title: Association Between Albumin Administration and Improved Survival and Organ Function in Adult Patients Undergoing Cardiac Surgery With Cardiopulmonary Bypass
The invesitgators utilized the Cerner HealthFacts database (a large HIPAA-compliant clinical-administrative database maintained by Cerner Inc., USA) to identify a cohort of 6,249 adults that underwent on-pump cardiac surgery for valve and/or coronary artery procedures between January 2001 and March 2013. Of these, the investigators selected 1136 patients who received 5% albumin on the day of or the day following cardiac surgery and matched them (1:1) with 1136 patients who did not receive albumin. Characteristics on which patients were matched included patient demographic, hospital and procedural characteristics, baseline patient comorbidities including preoperative CKD and 26 other grouped conditions, as well as acute severity of illness at admission to ICU.
Read the detailed description
Following development of the study plan and project summary, approval was obtained (November 25th 2013) from the Duke University Medical Center institutional review board, who reviewed the study outline, including endpoints and treatment exposure groups prior to data extraction. HIPAA-compliant data were then extracted from the U.S. Cerner HealthFacts®, (Cerner Corp., Kansas City, MO) database. Patients who underwent cardiac surgery utilizing CPB between Jan 2001 and March 2013 were identified. In addition to hospital characteristics (bed-size, teaching status, location), encounter-level patient data (demographics, admission source, payer), comprehensive time-stamped medication orders, pharmacy records, laboratory results, admission and discharge diagnoses (International Classification of Diseases Ninth Revision Clinical Modification, ICD-9-CM codes) and procedures were available.
Study Population Adults that underwent isolated valve, isolated CABG or two or more procedures utilizing CPB, and who survived for at-least 24 hours were eligible for inclusion (except when CABG was performed emergently following a PCI). Procedures were identified using ICD-9-CM codes (39.61 = extracorporeal circulation auxiliary to open heart surgery) or CPT codes (indicating 'on-pump' surgery). Patients with missing or incomplete admission, procedure, and/or discharge dates, gender, and age were excluded. Discrete encounters less than four hours apart within the same hospital system, were considered contiguous. We also excluded those patients undergoing heart transplantation (ICD-9 procedure code 37.51) or with any of the following Elixhauser comorbidities: AIDS, lymphoma, metastatic cancer, solid tumors without metastases. Only the first operative procedure during this time was considered and patients undergoing multiple non-contiguous procedures were excluded.
Definition of Exposure The study cohort consisted of patients that had either received at least 500mL of any crystalloid (0.9% saline, buffered salt solutions such as Plasma-Lyte, Lactated Ringers etc.) with or without any volume of 5% albumin - the 'albumin' and 'crystalloid only' cohorts respectively. All intravenous fluids documented on the day of or the day following surgery were considered in order to determine eligibility for inclusion, and fluid volumes from the day of through two days following surgery were monitored. The investigators excluded crystalloids administered in smaller containers (<=250mL volume) as these were most likely to be used for medication delivery rather than for the maintenance of hydration or expansion of intravascular blood volume in this adult population. Such volume thresholds were not imposed for colloids in the 'albumin' cohort however. Patients were excluded from the study if they received any other colloid (e.g. albumin over 5% concentration or hydroxyethyl starch) or hypertonic saline. Patients were not excluded from the albumin arm if they received plasma protein fraction (PPF) however.
Definition of Outcomes The primary outcome was in-hospital mortality during the index admission in which cardiac surgery was performed. The investigators also examined in-hospital mortality within 30, 60, and 90 days after the index procedure. Secondary endpoints included major postoperative adverse cardiac, renal, hepatic, metabolic, pulmonary, neurologic, hematologic, or infectious events defined using clinical parameters or administrative codes (ICD-9-CM). Additional administrative secondary outcomes included: Length-of-stay, readmissions, and re-operations (return to operating room). MACE at 30, 60 and 90 days were calculated from four separate binary categories: 1) in-hospital mortality; 2) post-operative stroke or cerebrovascular accident per ICD-9 diagnosis codes not present-on-admission for the index visit or for subsequent visits within respective MACE timeframes; 3) post-operative revascularization or PCI; and 4) post-operative myocardial infarction. A composite binary indicator was also reported for any one or greater MACE condition met within the respective timeframes.
- Conditions
- Thoracic Surgery
- Being tested
- Albumin
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
AlbuminDrug
patients that had either received any volume of 5% albumin in addition to at least 500mL of any crystalloid (0.9% saline, buffered salt solutions such as Plasma-Lyte, Lactated Ringers etc.)
| Study group | Role | What they receive |
|---|---|---|
| Albumin | patients that had received at least 500mL of any crystalloid (0.9% saline, buffered salt solutions such as Plasma-Lyte, Lactated Ringers etc.) with any volume of 5% albumin Receives: Drug: Albumin | |
| Crystalloid Only | patients that had received at least 500mL of any crystalloid (0.9% saline, buffered salt solutions such as Plasma-Lyte, Lactated Ringers etc.) without any volume of 5% albumin |
What is being measured
The primary outcome is the main question the study is designed to answer.
In-hospital mortality
patients in either cohort who died during index admission to hospital at any time point from POD 0 until day of discharge or POD 29.
Measured: any time point during index admission to hospital from post operative day (POD) 1 until discharge from hospital or POD 29
Secondary outcomes (3)
30, 60, and 90 day mortality
mortality rate for all patients in both cohorts at 30, 60, and 90 days from POD 0
Measured: 30, 60, and 90 days from POD 1
Major Adverse Cardiac Events (MACE)
MACE at 30, 60 and 90 days were calculated from four separate binary categories: 1) in-hospital mortality; 2) post-operative stroke or cerebrovascular accident per ICD-9 diagnosis codes not present-on-admission for the index visit or for subsequent visits within respective MACE timeframes; 3) post-operative revascularization or PCI; and 4) post-operative myocardial infarction.
Measured: 30, 60, and 90 days from POD 0
Acute Kidney Injury
Acute Kidney Injury Network (AKIN) serum creatinine (SCr) scores were calculated based on a combination of absolute SCr levels as well as relative SCr increases compared to baseline (greater numeric score indicates greater injury). Baseline SCr was set as the most recent reading within a 30 day period prior to surgery. In the case of lab values with exactly the same timestamp, the lowest SCr value was chosen. In the case of missing or insufficient SCr data, patients were deemed unevaluable rather than assumed to have a normal SCr reading. All AKIN scores are presented without respect to administration/non-administration of preoperative diuretics. Quantitative urine output values, required for an AKIN urine evaluation component, were not captured in the database for any patient and therefore were not included. The SCr criteria of AKIN were utilized, (which stages severity as 1, 2, or 3)
Measured: daily from POD 0 until discharge from hospital from index procedure, on average 14 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Aug 2016 (estimated)
- Study startJan 2012
- Primary completionMar 2013
- Study completionMar 2013
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Thoracic SurgeryStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Retrospective
- Enrolment
- 6,249 participants (actual)
Sponsor and investigators
- Lead sponsor
- Vanderbilt University
- Sponsor type
- University, hospital or other
- Collaborators
- Duke University, Grifols Biologicals, LLC
- Responsible party
- Principal investigator, Adam Kingeter, Vanderbilt University
- Investigators
- Adam kingeter, MD, Principal investigator, Vanderbilt University Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02878733
- Sponsor's protocol ID
- Pro00050804
- Status last verified
- Aug 2016
- First submitted
- 16 Aug 2016
- Last updated
- 25 Aug 2016
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- No: Individual data are de-identified
Study at a glance
From the registry record, last updated by the sponsor on 25 Aug 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Association Between Albumin Administration and Improved Survival and Organ Function in Adult Patients Undergoing Cardiac Surgery With Cardiopulmonary Bypass
- ClinicalTrials.gov ID
- NCT02878733
- Acronym / sponsor ID
- Pro00050804
- Conditions
- Thoracic Surgery
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 6,249 participants (actual)
- Lead sponsor
- Vanderbilt UniversityUniversity, hospital or other
- Collaborators
- Duke University, Grifols Biologicals, LLC
- Study start
- Jan 2012
- Primary completion
- Mar 2013 (actual)
- Study completion
- Mar 2013 (actual)
- First posted
- 25 Aug 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The invesitgators utilized the Cerner HealthFacts database (a large HIPAA-compliant clinical-administrative database maintained by Cerner Inc., USA) to identify a cohort of 6,249 adults that underwent on-pump cardiac surgery for valve and/or coronary artery procedures between January 2001 and March 2013. Of these, the investigators selected 1136 patients who received 5% albumin on the day of or the day following cardiac surgery and matched them (1:1) with 1136 patients who did not receive albumin. Characteristics on which patients were matched included patient demographic, hospital and procedural characteristics, baseline patient comorbidities including preoperative CKD and 26 other grouped conditions, as well as acute severity of illness at admission to ICU.
Detailed description
Following development of the study plan and project summary, approval was obtained (November 25th 2013) from the Duke University Medical Center institutional review board, who reviewed the study outline, including endpoints and treatment exposure groups prior to data extraction. HIPAA-compliant data were then extracted from the U.S. Cerner HealthFacts®, (Cerner Corp., Kansas City, MO) database. Patients who underwent cardiac surgery utilizing CPB between Jan 2001 and March 2013 were identified. In addition to hospital characteristics (bed-size, teaching status, location), encounter-level patient data (demographics, admission source, payer), comprehensive time-stamped medication orders, pharmacy records, laboratory results, admission and discharge diagnoses (International Classification of Diseases Ninth Revision Clinical Modification, ICD-9-CM codes) and procedures were available.
Study Population Adults that underwent isolated valve, isolated CABG or two or more procedures utilizing CPB, and who survived for at-least 24 hours were eligible for inclusion (except when CABG was performed emergently following a PCI). Procedures were identified using ICD-9-CM codes (39.61 = extracorporeal circulation auxiliary to open heart surgery) or CPT codes (indicating 'on-pump' surgery). Patients with missing or incomplete admission, procedure, and/or discharge dates, gender, and age were excluded. Discrete encounters less than four hours apart within the same hospital system, were considered contiguous. We also excluded those patients undergoing heart transplantation (ICD-9 procedure code 37.51) or with any of the following Elixhauser comorbidities: AIDS, lymphoma, metastatic cancer, solid tumors without metastases. Only the first operative procedure during this time was considered and patients undergoing multiple non-contiguous procedures were excluded.
Definition of Exposure The study cohort consisted of patients that had either received at least 500mL of any crystalloid (0.9% saline, buffered salt solutions such as Plasma-Lyte, Lactated Ringers etc.) with or without any volume of 5% albumin - the 'albumin' and 'crystalloid only' cohorts respectively. All intravenous fluids documented on the day of or the day following surgery were considered in order to determine eligibility for inclusion, and fluid volumes from the day of through two days following surgery were monitored. The investigators excluded crystalloids administered in smaller containers (<=250mL volume) as these were most likely to be used for medication delivery rather than for the maintenance of hydration or expansion of intravascular blood volume in this adult population. Such volume thresholds were not imposed for colloids in the 'albumin' cohort however. Patients were excluded from the study if they received any other colloid (e.g. albumin over 5% concentration or hydroxyethyl starch) or hypertonic saline. Patients were not excluded from the albumin arm if they received plasma protein fraction (PPF) however.
Definition of Outcomes The primary outcome was in-hospital mortality during the index admission in which cardiac surgery was performed. The investigators also examined in-hospital mortality within 30, 60, and 90 days after the index procedure. Secondary endpoints included major postoperative adverse cardiac, renal, hepatic, metabolic, pulmonary, neurologic, hematologic, or infectious events defined using clinical parameters or administrative codes (ICD-9-CM). Additional administrative secondary outcomes included: Length-of-stay, readmissions, and re-operations (return to operating room). MACE at 30, 60 and 90 days were calculated from four separate binary categories: 1) in-hospital mortality; 2) post-operative stroke or cerebrovascular accident per ICD-9 diagnosis codes not present-on-admission for the index visit or for subsequent visits within respective MACE timeframes; 3) post-operative revascularization or PCI; and 4) post-operative myocardial infarction. A composite binary indicator was also reported for any one or greater MACE condition met within the respective timeframes.
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Albumin | – | Drug: Albuminpatients that had received at least 500mL of any crystalloid (0.9% saline, buffered salt solutions such as Plasma-Lyte, Lactated Ringers etc.) with any volume of 5% albumin |
| Crystalloid Only | – | –patients that had received at least 500mL of any crystalloid (0.9% saline, buffered salt solutions such as Plasma-Lyte, Lactated Ringers etc.) without any volume of 5% albumin |
Who may qualify
- Ages
- 18 to 85 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Adults that underwent isolated valve, isolated CABG or two or more procedures utilizing CPB
Key inclusion criteria (1 listed)
- Adults that underwent isolated valve, isolated CABG or two or more procedures utilizing CPB
Key exclusion criteria (4 listed)
- death within 24 hours of index procedure
- patients undergoing heart transplantation
- Patients with missing or incomplete admission, procedure, and/or discharge dates, gender, and age were excluded
- patients with any of the following Elixhauser comorbidities: AIDS, lymphoma, metastatic cancer, solid tumors without metastases
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Albuminpatients that had either received any volume of 5% albumin in addition to at least 500mL of any crystalloid (0.9% saline, buffered salt solutions such as Plasma-Lyte, Lactated Ringers etc.) | Drug | Albumin |
Primary outcome
In-hospital mortality
Time frame: any time point during index admission to hospital from post operative day (POD) 1 until discharge from hospital or POD 29
patients in either cohort who died during index admission to hospital at any time point from POD 0 until day of discharge or POD 29.
3 secondary outcomes
30, 60, and 90 day mortality
Time frame: 30, 60, and 90 days from POD 1
Major Adverse Cardiac Events (MACE)
Time frame: 30, 60, and 90 days from POD 0
Acute Kidney Injury
Time frame: daily from POD 0 until discharge from hospital from index procedure, on average 14 days
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Aug 2016.
- Individual participant dataSharing planned: No. Individual data are de-identified
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Adam kingeter, MD principal investigator
Vanderbilt University Medical Center
Questions about this trial
What is this clinical trial studying?
An observational study of Thoracic Surgery, run by Vanderbilt University.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 25 Aug 2016. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
In-hospital mortality (time frame: any time point during index admission to hospital from post operative day (POD) 1 until discharge from hospital or POD 29). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Aug 2016.