Home Print this page Email this page Small font sizeDefault font sizeIncrease font size
Users Online: 576

 

Home  | About Us | Editors | Search | Ahead Of Print | Current Issue | Archives | Submit Article | Instructions | Subscribe | Contacts | Login 
     


 
 
Table of Contents
ORIGINAL ARTICLE
Year : 2020  |  Volume : 10  |  Issue : 5  |  Page : 33-38

Impact of critical care response team implementation on oncology patient outcomes: A retrospective cohort study


1 Department of Critical Care Medicine, College of Medicine, King Saud Bin AbdulAziz University for Health Sciences; Department of Intensive Care, King Abdulaziz Medical City, National Guard Hospital, Riyadh, Saudi Arabia
2 Department of Internal Medicine and Thrombosis, King Abdulaziz Medical City, National Guard Hospital, Riyadh, Saudi Arabia
3 Department of Infection Prevention and Control, King Abdulaziz Medical City, National Guard Hospital; Department of Epidemiology and Biostatistics, College of Public Health and Health Informatics, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia

Date of Submission07-Mar-2019
Date of Acceptance07-Apr-2020
Date of Web Publication16-Sep-2020

Correspondence Address:
Dr. Saad Al Qahtani
Department of Critical Care Medicine, College of Medicine, King Saud Bin AbdulAziz University for Health Sciences, Riyadh; Intensive Care Department, King Abdulaziz Medical City, National Guard Hospital, P.O. Box: 22490, Riyadh 11426
Saudi Arabia
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/IJCIIS.IJCIIS_13_19

Rights and Permissions
   Abstract 


Introduction: The main goal of a critical care response team (CCRT) is to quickly assess and transfer, if required, rapidly deteriorating patients to an intensive care unit (ICU) to prevent cardiopulmonary arrest, stabilize patients' condition, and help in optimizing the care provided by the primary team. The objective of this study was to investigate the correlation between early intervention by CCRT and the outcome of oncology patients.
Materials and Methods: This is a retrospective cohort study conducted at King Abdulaziz Medical City (KAMC), Riyadh, Saudi Arabia. KAMC is a tertiary care facility with 1200-bed capacity. The study compared oncology patients to nononcology patients.
Results: Over 4 years, a total number of 4941 patients were reviewed, of which 172 were oncology patients. The average age of patients in the oncology group was 48.8 ± 20.7, while the average age for nononcology was 52.8 ± 21.2 (P = 0.016). The average Acute Physiology and Chronic Health Evaluation II score on admission for oncology patients was higher than that for the nononcology group (27.8 ± 8.9 vs. 23.6 ± 9.3, respectively). Lower ICU mortality was seen after CCRT implementation (38.8% vs. 62.7%). The average duration of hospital stay and ICU stay increased after CCRT implementation (37.34 vs. 29.31 and 11.93 vs. 8.9, respectively).
Conclusion: In this study, we identified that early intervention by implementing CCRT had a significant impact in reducing ICU mortality for oncology and nononcology patients.

Keywords: Cancer, critical care response team, oncology


How to cite this article:
Al Qahtani S, Alaklabi A, El-Saed A. Impact of critical care response team implementation on oncology patient outcomes: A retrospective cohort study. Int J Crit Illn Inj Sci 2020;10:33-8

How to cite this URL:
Al Qahtani S, Alaklabi A, El-Saed A. Impact of critical care response team implementation on oncology patient outcomes: A retrospective cohort study. Int J Crit Illn Inj Sci [serial online] 2020 [cited 2023 Mar 27];10:33-8. Available from: https://www.ijciis.org/text.asp?2020/10/5/33/295211




   Introduction Top


Due to the expanding role of intensive care unit (ICU) over the past 20 years, the care of critically ill patients in ICUs has become the responsibility of specialized critical care personnel.[1] A rapid response system (RRS) was established to ensure timely interventions for hospitalized patients and to detect acutely deteriorating patients; this system aims to prevent patient deterioration and unexpected deaths due to clinical errors.[2],[3],[4] RRS can be referred to as a critical care team, medical emergency team, or a rapid response team.[3] Several studies have demonstrated the necessity of an RRS system for reducing the morbidity and mortality of patients.[5],[6],[7],[8],[9]

The effects and benefits of a critical care response team (CCRT) on patient care can be observed in the resuscitation and identification of rapidly deteriorating patients.[10] Addressing the do-not-resuscitate (DNR) status for patients in the ward is a new role of the CCRT and has been explored during the process of implementation of teams.[11]

Identifying DNR cases early results in the prevention of unnecessary admissions to ICUs.[10]

Advances in early diagnosis and aggressive management of cancer have improved long-term outcomes.[12] However, some cancer patients develop several complications and/or treatment-associated side effects[13] which often require multidisciplinary care in an ICU.[14],[15] Early admission to an ICU has been associated with lower mortality rates when compared to late admissions for the general ICU population.[16] The same was found in critically ill cancer patients, and late ICU admission was associated with increased mortality.[17],[18] Improving the outcome in critically ill cancer patients may occur by early intervention, before ICU admission and the development of severe organ failure.[19] However, there is currently a lack of evidence on the outcome of early intervention of a CCRT on cancer patients.

CCRTs at the Ministry of National Guard Health Affairs hospitals were initiated in 2007. The main goal of the CCRT is to quickly assess and transfer, if required, rapidly deteriorating patients to the ICU to prevent cardiopulmonary arrest, stabilize patients' condition, and help in optimizing the care provided by the primary team. The objective of this study is to determine the correlation between early intervention and late intervention by CCRT and compare the outcome of oncology patients to nononcology patients.


   Materials and Methods Top


Setting

This is a retrospective cohort study conducted at King Abdulaziz Medical City (KAMC), a tertiary care teaching hospital in Riyadh, Kingdom of Saudi Arabia. KAMC is a 1200-bed capacity tertiary care facility with 9 different ICUs.

Populations

Patients admitted both before and after early intervention by CCRT were included in the study. The study included all adult patients over the age of 16 years. Eligibility for patient inclusion was based on the CCRT calling criteria which include respiratory rate >30 breath/min or <8 breaths/min or oxygen saturation ≤90%, systolic blood pressure ≤90 or ≥200 mmHg, heart rate ≤40 or ≥130 beats/min, urine output ≤100 mL over 4 h, decreased level of consciousness by ≥2 points on the Glasgow Come Scale (GCS) or repeated seizures, and any serious concern about the patient's clinical condition. All patients were from general wards (non-ICU patients). All eligible ward patients were followed in the ward or in the ICU, if admitted, until patient discharge from the hospital or death.

Study design

Data were collected over a 5-year timeframe, from 2006 to 2010. The data from January 1, 2006, to November 23, 2007, were the pre-CCRT period, and the data from December 1, 2007, to December 31, 2010, were the post-CCRT period. The study compared the demographics and outcome between oncology and nononcology patients before and after CCRT implementation. All patients received follow-up during their stay in the hospital, and no follow-up occurred after discharge. Patients who were kept in ICU only for observation and monitoring and any incomplete case records were excluded from the study.

Statistical analysis

Statistical analysis was done using IBM® SPSS version 16.0 statistical software package (IBM Corp, Armonk, USA). Variables were presented as frequencies and percentages for qualitative data, while mean and standard deviation were used for quantitative data. The Acute Physiology and Chronic Health Evaluation II (APACHE II) was utilized when classifying the severity of disease. Student's t-test was used to compare quantitative variables; Chi-square test was used for comparing qualitative variables between the groups. P ≤ 0.05 was considered statistically significant.


   Results Top


The present study included 4941 patients, of which 172 were oncology and 4769 were nononcology patients. Patient demographics and clinical characteristics are shown in [Table 1]. For oncology patients, the average age was 48.8 ± 20.7, while the average age for the nononcology patients was 52.8 ± 21.2; there was a significant difference between the two groups. Patients were classified into three age groups: patients younger than 41, patients between 41 and 65 years old, and patients older than 65 years. There was a significant difference between oncology and nononcology patients younger than 41 years of age [Table 1].
Table 1: Demographics and clinical characteristics of patients at the Ministry of National Guard Health Affairs hospitals in Saudi Arabia (2006-2010)

Click here to view


As shown in [Table 2], the majority of the patients were admitted for cardiovascular diseases, postoperative care, and respiratory diseases. However, there were significant differences between oncology and nononcology admission categories. The majority of the patients were referred from the floor. A significant difference for referral reasons can be seen between both the groups [Table 2]. The mean APACHE II score on admission for the oncology group was higher (27.8 ± 8.9) than the nononcology group (23.6 ± 9.3). The majority of the oncology patients (41.6%) had a score of 21–30, while the majority of the nononcology patients (40.2%) had a score of ≤20 [P < 0.001, [Table 2]. The average score of GCS for oncology patients was higher (10.9 ± 4.8) than the score for nononcology patients (9.4 ± 4.4, P < 0.001). There was a significant difference between both the patient groups in all chronic health points, liver disease, cardiovascular disease, respiratory disease, renal disease, and immune-comprised patients. Diabetes was more prevalent in nononcology patients (36.1%) than oncology patients (22.7%). [Table 2] shows that no code oncology patients accounted for 36.6% of the patients, while no code nononcology patients accounted for 18.5% of the patients. There was a significant difference in APACHE II scores between oncology and nononcology patients [P < 0.001, [Table 2].
Table 2: Clinical characteristics of patients upon admission to the Ministry of National Guard Health Affairs hospitals in Saudi Arabia (2006-2010)

Click here to view


The outcome of oncology and nononcology patients before and after CCRT implementation is shown in [Table 3]. In oncology patients, there was a significant difference in ICU mortality, duration of hospital stay, and duration of post-ICU stay (P = 0.004, P = 0.034, and P = 0.004, respectively). Less mortality in ICUs was seen after CCRT implementation (38.8%) than before CCRT [62.7%, [Table 3]. The average hospital duration and post-ICU duration increased after CCRT compared to before CCRT (37.34% vs. 29.31% and 11.93% vs. 8.9%, respectively). In nononcology patients, there were significant differences in hospital mortality, tracheostomy, and readmission. Hospital mortality, tracheostomy, and readmission rates decreased after the implementation of CCRT [Table 3]. Hospital mortality decreased after CCRT implementation from 38.5% to 33.9%, and less patients required tracheostomy after CCRT compared to before CCRT (15.9% vs. 19.1%, respectively). After CCRT, fewer patients required readmission compared to before CCRT [11.1% vs. 13.6%, respectively; [Table 3].
Table 3: Outcome of oncology and nononcology patients before and after critical care response team implementation at the Ministry of National Guard Health Affairs hospitals in Saudi Arabia (2006-2010)

Click here to view


When comparing the two groups of patients: oncology and nononcology groups, significances were found in ICU mortality, hospital mortality, tracheostomy, sepsis, post-ICU duration, pre-ICU duration, and ventilation days. ICU mortality was less in nononcology patients (22%) than oncology patients (38.8%) after CCRT. In addition, hospital mortality was less in nononcology patients (33.9%) than oncology patients (55.4%) after CCRT. More nononcology patients (15.9%) required a tracheostomy than oncology patients (4.1%). Sepsis was increased in oncology patients (71.7%) compared to nononcology patients (27.5%) after CCRT. The average post-ICU duration and ventilation days were less in oncology patients (11.93% and 5.59%, respectively) than in nononcology patients (34.08% and 7.18%, respectively) after CCRT, while the average pre-ICU duration was increased in oncology patients (18.36%) when compared to nononcology patients (12.06%) after CCRT.


   Discussion Top


This is the first study to investigate the outcome of early intervention of CCRT on oncology patients. CCRT is a team of specially trained clinical personnel capable of providing critical care for patients bedside and preventing the deterioration of patients' status.[20]

Several reports showed that the range of ICU mortality rates of critically ill oncology patients was 15.9%–32%.[19],[21],[22] The ICU mortality rate of oncology patients was reported to be 27% in European ICUs.[23] Several indicators of poor prognosis in cancer were reported including older age, high APACHE II scores, and sepsis.[24]

Patients from the nononcology group were significantly older than those from the oncology group, specifically for those older than 65 years of age. In addition, they had a higher average BMI compared to patients from the oncology group. Males were more prevalent in both the groups. Admission of oncology and nononcology patients was mainly due to cardiovascular reasons, followed by respiratory reasons for oncology patients and postoperative reasons for nononcology patients. The majority of the patients in both the groups were admitted to ICU nonoperatively for medical reasons referred from the floor. It was reported that APACHE II scores were fairly accurate at predicting ICU mortality of critically ill oncology patients with acceptable calibration and good discrimination.[21],[25] The average APACHE II score for oncology patients was significantly higher than that of nononcology patients, with a significant dominance of score 21–30 in oncology patients and dominance of score ≤20 in nononcology patients.

In the present study, we investigated the outcome of both the groups before and after CCRT and then compared them with each other. ICU mortality rates significantly decreased in oncology patients after CCRT, while no difference was found in nononcology patients; there was a significant difference between the two groups. Nononcology patients had lower APACHE II score compared to oncology ones.[26]

Hospital mortality decreased after CCRT in both the groups with no significance in the mortality rate in oncology patients and a significant decrease in nononcology patients; there was a significant difference between the two groups. A study from a tertiary care oncology hospital reported that mortality rates decreased after the introduction of CCRT.[27] The present study showed no significant difference in outcome before and after CCRT in each group and between the two groups regarding cardiovascular arrest, ventilator use, and readmission within 48 h.

In a previous study, it was found that cardiac arrest slightly decreased after the introduction of CCRT.[27]

The rate of performing tracheostomy was decreased after CCRT in both the groups without significance in oncology patients and with significance in nononcology patients, while there was a significant difference between the two groups. Readmission of patients was significantly decreased after CCRT in nononcology patients, while no significant difference was found in oncology patients.

Oncology patients were found to have an increased risk of sepsis compared to other patients which may be due to the immunosuppression caused by treatment of malignancy or malignancy itself.[17],[23],[28] Oncology patients have a fourfold increase in severe sepsis in comparison to noncancer patients with 16.4/1000 cancer cases.[28],[29] The present study revealed that the sepsis rate after CCRT significantly decreased in nononcology patients while slightly increasing in oncology patients; there was a significant difference between the two groups.

In a previous study,[27] it was found that the introduction of a CCRT in a tertiary-care oncology hospital had no significant effect on the hospital length of stay. However, the current study found that the average hospital duration was significantly increased after CCRT in the oncology group. No difference was found between oncology and nononcology for hospital duration. Increased hospital duration may be contributed to the influence of CCRT on the primary teams' decision for the required length of care.[30] In addition, the tracheostomy rate after CCRT was significantly increased in nononcology patients (P < 0.001) which required further management by multidisciplinary teams (speech therapist, swallowing assessment, and tracheostomy education). No significant difference was found in ICU duration after CCRT in either group or between both the groups.[31] The average duration of post-ICU significantly decreased after CCRT in oncology patients, while no significant difference was found in nononcology patients. However, there was a significant difference between the two groups. The average ventilation days slightly decreased in oncology patients while remaining constant in nononcology; there was a significant difference between the oncology and nononcology groups.

This study found a positive outcome of CCRT intervention in oncology and nononcology patients. The ICU mortality rate was significantly decreased after CCRT implementation in oncology patients. Further studies are recommended to fully understand the benefits of CCRT intervention in oncology and nononcology patients, as this is the first study to evaluate the outcome of early intervention of oncology patients after CCRT implementation.

Research quality and ethics statement

The authors of this manuscript declare that this scientific work complies with reporting quality, formatting, and reproducibility guidelines set forth by the EQUATOR Network. The authors also attest that this clinical investigation was determined to require Institutional Ethics Committee, Research Cell, King George's Medical University, Lucknow and appropriate approval (84th ECM II-B-Thesis) was granted by the Research Cell, King George's Medical University, Lucknow.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

Ethical conduct of research

This study was approved by the Institutional Review Board / Ethics Committee. The authors followed applicable EQUATOR Network (http://www.equator-network.org/) guidelines during the conduct of this research project.



 
   References Top

1.
Mercer M, Robinson H. Outreach and the evolution of critical care. Anaesthesia 2010;65:754.  Back to cited text no. 1
    
2.
Berwick DM, Calkins DR, McCannon CJ, Hackbarth AD. The 100,000 lives campaign: Setting a goal and a deadline for improving health care quality. JAMA 2006;295:324-7.  Back to cited text no. 2
    
3.
Lee YJ, Lee DS, Min H, Choi YY, Lee EY, Song I, et al. Differences in the clinical characteristics of rapid response system activation in patients admitted to medical or surgical services. J Korean Med Sci 2017;32:688-94.  Back to cited text no. 3
    
4.
Al Qahtani S. Satisfaction survey on the critical care response team services in a teaching hospital. Int J Gen Med 2011;4:221-4.  Back to cited text no. 4
    
5.
DeVita MA, Braithwaite RS, Mahidhara R, Stuart S, Foraida M, Simmons RL, et al. Use of medical emergency team responses to reduce hospital cardiopulmonary arrests. Qual Saf Health Care 2004;13:251-4.  Back to cited text no. 5
    
6.
Buist MD, Moore GE, Bernard SA, Waxman BP, Anderson JN, Nguyen TV. Effects of a medical emergency team on reduction of incidence of and mortality from unexpected cardiac arrests in hospital: Preliminary study. BMJ 2002;324:387-90.  Back to cited text no. 6
    
7.
Bellomo R, Goldsmith D, Uchino S, Buckmaster J, Hart GK, Opdam H, et al. A prospective before-and-after trial of a medical emergency team. Med J Aust 2003;179:283-7.  Back to cited text no. 7
    
8.
Chan PS, Khalid A, Longmore LS, Berg RA, Kosiborod M, Spertus JA. Hospital-wide code rates and mortality before and after implementation of a rapid response team. JAMA 2008;300:2506-13.  Back to cited text no. 8
    
9.
Sharek PJ, Parast LM, Leong K, Coombs J, Earnest K, Sullivan J, et al. Effect of a rapid response team on hospital-wide mortality and code rates outside the ICU in a Children's Hospital. JAMA 2007;298:2267-74.  Back to cited text no. 9
    
10.
Gouda AM, Alqahtani SM. Do not resuscitate: An expanding role for critical care response team. Indian J Crit Care Med 2016;20:146-9.  Back to cited text no. 10
[PUBMED]  [Full text]  
11.
Jones DA, McIntyre T, Baldwin I, Mercer I, Kattula A, Bellomo R. The medical emergency team and endoflife care: A pilot study. Crit Care Res 2007;9:151-6.  Back to cited text no. 11
    
12.
Brenner H. Long-term survival rates of cancer patients achieved by the end of the 20th century: A period analysis. Lancet 2002;360:1131-5.  Back to cited text no. 12
    
13.
Song JU, Suh GY, Park HY, Lim SY, Han SG, Kang YR, et al. Early intervention on the outcomes in critically ill cancer patients admitted to intensive care units. Intensive Care Med 2012;38:1505-13.  Back to cited text no. 13
    
14.
Azoulay E, Afessa B. The intensive care support of patients with malignancy: Do everything that can be done. Intensive Care Med 2006;32:3-5.  Back to cited text no. 14
    
15.
Darmon M, Azoulay E. Critical care management of cancer patients: Cause for optimism and need for objectivity. Curr Opin Oncol 2009;21:318-26.  Back to cited text no. 15
    
16.
Sprung CL, Geber D, Eidelman LA, Baras M, Pizov R, Nimrod A, et al. Evaluation of triage decisions for intensive care admission. Crit Care Med 1999;27:1073-9.  Back to cited text no. 16
    
17.
Thiéry G, Azoulay E, Darmon M, Ciroldi M, De Miranda S, Lévy V, et al. Outcome of cancer patients considered for intensive care unit admission: A hospital-wide prospective study. J Clin Oncol 2005;23:4406-13.  Back to cited text no. 17
    
18.
Peigne V, Rusinová K, Karlin L, Darmon M, Fermand JP, Schlemmer B, et al. Continued survival gains in recent years among critically ill myeloma patients. Intensive Care Med 2009;35:512-8.  Back to cited text no. 18
    
19.
Azoulay E, Soares M, Darmon M, Benoit D, Pastores S, Afessa B. Intensive care of the cancer patient: Recent achievements and remaining challenges. Ann Intensive Care 2011;1:5.  Back to cited text no. 19
    
20.
Al Shimemeri A. Implementation of critical care response team. Int J Crit Illn Inj Sci 2014;4:156-61.  Back to cited text no. 20
    
21.
McGrath S, Chatterjee F, Whiteley C, Ostermann M. ICU and 6-month outcome of cancer patients in the intensive care unit. QJM 2010;103:397-403.  Back to cited text no. 21
    
22.
Ñamendys-Silva SA, González-Herrera MO, Herrera-Gómez A. Mortality of patients with cancer admitted to intensive care unit. Am J Hosp Palliat Care 2013;30:214-5.  Back to cited text no. 22
    
23.
Taccone FS, Artigas AA, Sprung CL, Moreno R, Sakr Y, Vincent JL. Characteristics and outcomes of cancer patients in European ICUs. Crit Care 2009;13:R15.  Back to cited text no. 23
    
24.
Suhag V, Sarin A, Singh AK. Intensive care for cancer patients: An overview. Austral Asian J Cancer 2014:13:193-201.  Back to cited text no. 24
    
25.
Kopterides P, Liberopoulos P, Ilias I, Anthi A, Pragkastis D, Tsangaris I, et al. General prognostic scores in outcome prediction for cancer patients admitted to the intensive care unit. Am J Crit Care 2011;20:56-66.  Back to cited text no. 25
    
26.
Loh KP, Kansagra A, Shieh MS, Pekow P, Lindenauer P, Stefan M, et al. Predictors of in-hospital mortality in patients with metastatic cancer receiving specific critical care therapies. J Natl Compr Canc Netw 2016;14:979-87.  Back to cited text no. 26
    
27.
Heffer MJ, Lapinsky SE. Analysis of the utility of a critical care response team in a tertiary care oncology hospital. Chest 2008;134:s48001.  Back to cited text no. 27
    
28.
Ñamendys-Silva SA, González-Herrera MO, Texcocano-Becerra J, Herrera-Gómez A. Clinical characteristics and outcomes of critically ill cancer patients with septic shock. QJM 2011;104:505-11.  Back to cited text no. 28
    
29.
Fullerton JN, Perkins GD. Who to admit to intensive care? Clin Med (Lond) 2011;11:601-4.  Back to cited text no. 29
    
30.
Karpman C, Keegan MT, Jensen JB, Bauer PR, Brown DR, Afessa B. The impact of rapid response team on outcome of patients transferred from the ward to the ICU: A single-center study. Crit Care Med 2013;41:2284-91.  Back to cited text no. 30
    
31.
Kenward G, Castle N, Hodgetts T, Shaikh L. Evaluation of a medical emergency team one year after implementation. Resuscitation 2004;61:257-63.  Back to cited text no. 31
    



 
 
    Tables

  [Table 1], [Table 2], [Table 3]



 

Top
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
    Abstract
   Introduction
    Materials and Me...
   Results
   Discussion
    References
    Article Tables

 Article Access Statistics
    Viewed1312    
    Printed74    
    Emailed0    
    PDF Downloaded48    
    Comments [Add]    

Recommend this journal