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Volume 11, Issue 2, Pages 115-125 (June 2010)


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Nurses’ Evaluations of the Feasibility and the Clinical Utility of the Critical-Care Pain Observation Tool

Céline Gélinas, RN, PhDCorresponding Author Informationemail address

Received 14 January 2009; received in revised form 1 May 2009; accepted 18 May 2009. published online 22 September 2009.

Abstract 

Feasibility and clinical utility are essential characteristics to consider when it comes to developing or selecting a pain assessment tool to implement into practice. However, these characteristics have not been widely studied with available pain assessment tools in critically ill adults. The objective of this study was to describe nurses’ evaluations of the feasibility and clinical utility of the Critical-Care Pain Observation Tool (CPOT) in assessing pain in critically ill ventilated adults. A descriptive design was used. Of the 51 nurses who used the CPOT with the enrolled patients (n = 55), 33 returned their completed evaluation form. Overall, the feasibility and clinical utility of the CPOT were positively evaluated by the nurse participants. More than 90% of them supported that the directives about the use of the CPOT were clear and that it was simple to understand and easy to complete. Regarding its clinical utility, a little more than 70% of the nurses mentioned that the CPOT was helpful for nursing practice and recommended its use routinely. They acknowledged that the CPOT provided them with a common language and a standardized way to assess patients’ pain. Half of the nurse participants supported that the CPOT had influenced their practice. On the other hand, six nurses mentioned that they were already sensitive to nonverbal cues of pain before the introduction of the CPOT. In conclusion, the CPOT is a valid behavioral pain scale, which has been suggested by experts in recent critical reviews. So far, the CPOT is being used for research purposes and has been implemented into clinical practice of various health care centers of North America.

Article Outline

Abstract

Background

Aim

Methods

Design and Sample

Instruments

Critical-Care Pain Observation Tool

CPOT Evaluation Form

Procedure

Nurse Training

Data Collection

Data Analysis

Results

Nurse Participants

CPOT Feasibility and Clinical Utility

Discussion

Limitations

Future Directions

Conclusions

Acknowledgment

Appendix

Directives to Use the CPOT

Facial Expressions

References

Copyright

Pain is cited by patients as being a significant stressor in the critical care setting (Rotondi, Chelluri, Sirio, Mendelsohn, Schulz, et al., 2002). A thorough assessment tool is an important step in adequately managing pain. The patient's self-report of pain is considered to be the gold standard in pain assessment (IASP, 1979); however, it cannot always be obtained in the critically ill owing to such factors as sedation and mechanical ventilation (Kwekkeboom & Herr, 2001; Shannon & Bucknall, 2003). When the patient is unable to self-report pain, the use of a behavioral scale is highly recommended (Herr, Coyne, Key, Manworren, McCaffery, et al., 2006). Very few tools have been developed for critically ill nonverbal adults (Behavioral Pain Scale, [BPS] Payen, Bru, Bosson, Lagrasta, Novel et al., 2001; Critical-Care Pain Observation Tool, [CPOT] Gélinas, Fillion, Puntillo, Viens, & Fortier, 2006; PACU-BPRS Mateo & Krenzischek, 1992; and Pain Assessment and Intervention Notation, [PAIN] Puntillo, Miaskowski, Kehrle, Stannard, Gleeson, et al., 1997). Although the reliability and validity of most of these tools have been studied in critically ill adult samples, little has been done to document their feasibility and clinical utility despite the fact that these are crucial characteristics to consider in developing or selecting a tool to implement into practice.

The CPOT was recently developed and tested in critically ill adults of two university settings in the province of Quebec, Canada (Gélinas, Fillion, Puntillo, Viens, & Fortier, 2006; Gélinas & Johnston, 2007). Its content was derived from a literature review, chart review of critically ill adults (Gélinas, Fortier, Viens, Fillion, & Puntillo, 2004), and consultation with critical care nurses and physicians (Gélinas, Viens, Fortier, & Fillion, 2005). The item selection and content validity of the tool has been recently published (Gélinas, Fillion, & Puntillo, 2009). It demonstrated moderate to high interrater reliability (French version: weighted kappa 0.52 to 0.88; English version: intraclass correlation coefficients 0.80 to 0.93). Discriminant validity was supported with higher CPOT scores during a nociceptive procedure (turning) compared with rest or a nonnociceptive procedure (taking noninvasive blood pressure). For criterion validity, the patients’ self-reports of pain intensity were associated with the CPOT scores (e.g., correlation coefficients from 0.40 to 0.71, p ≤ .05). The CPOT also showed a sensitivity of 86% and a specificity of 78% during nociceptive exposure in critically ill postoperative adults (Gélinas, Harel, Fillion, Puntillo, & Johnston, 2009). Based on those results, the CPOT appears to be a useful tool for critically ill nonverbal patients. The present paper aims to describe the feasibility and clinical utility of the English version of the CPOT as evaluated by intensive care unit (ICU) nurses who were trained for its use for the purpose of its validation in a previous study (Gélinas & Johnston, 2007).

Background 

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A consensus has not yet been reached regarding the definitions of feasibility and clinical utility; as such, these concepts are sometimes used interchangeably (Stevens & Gibbins, 2002). Generally, feasibility refers to the ease with which the clinicians can apply the tool in the clinical setting (e.g., the tool is simple to understand, easy to complete, and quick to use) whereas clinical utility refers to the ability to use the results of the tool in a useful or informative way within the clinical setting (Duhn & Medves, 2004). Although reliability and validity testing of critical care pain assessment tools is well underway, to date the feasibility and clinical utility of only the PAIN algorithm (Puntillo, Stannard, Miaskowski, Kehrle, & Gleeson, 2002) and the BPS (Payen et al., 2001) have been explored.

The PAIN algorithm is a systematic pain assessment and management tool developed by a team of critical care nurses and pain experts (Puntillo et al., 2002). The first step consists of a checklist (present or absent) and a numeric rating scale (0 to 10) which prompts the nurse to assess whether or not the patient has pain. The checklist contains 20 items clustered in a behavioral dimension (movements, vocalization, facial indicators, and posturing/guarding) and a physiologic dimension (heart rate, blood pressure, respiratory rate, perspiration, and pallor), the latter being based on the nurse's clinical judgment. The pain assessment part of the PAIN was tested with 31 critically ill postoperative adult patients, most of them extubated (Puntillo et al., 1997). It showed acceptable criterion validity when the number of behavioral and physiologic indicators observed were compared with the nurse's ratings of pain intensity (r = 0.17 to 0.77; p < .05). The second and third steps of the algorithm involve assessing for potential problems influencing opioid administration and making an analgesic treatment decision. Of the eleven nurse evaluators who used the PAIN, ten found the instrument to be helpful (Puntillo et al., 2002). Their comments indicate that this was because it added structure to their practice and increased their awareness of pain indicators. Four nurses felt the instrument could be improved, and their comments speak to the need for reducing the length and complexity of the tool. Five nurses believed the algorithm changed their practice, and six felt that it would have a lasting effect on their practice. Ten nurses believed that they would have benefited from having the tool earlier in their practice, and eight felt that other nurses on the unit could benefit from it. In summary, although the PAIN appears to be a useful tool to standardize pain assessment and management in the ICU, some limitations have been highlighted. Namely, it does not standardize the measurements of behavioral and physiologic indicators, which are based on the nurse's clinical judgment, and the length of the tool limits its feasibility and clinical utility (Li, Puntillo, & Miaskowski, 2008).

The BPS was created to evaluate pain in critically ill sedated unconscious patients receiving mechanical ventilation (Payen et al., 2001). It takes into consideration three behavioral dimensions: facial expression, movement/positioning of upper limbs, and compliance with ventilation. Each behavior is scored from 1 to 4, for a possible total score ranging from 3 to 12. It was tested with three ICU mechanically ventilated and sedated adult samples: 30 trauma or postoperative patients (Payen et al., 2001), 30 medical patients (Aïssaoui, Zeggwagh, Zekraoui, Abidi, & Abouqal, 2005), and 44 medical or postoperative patients (Young, Siffleet, Nikoletti, & Shaw, 2006). All patients were unconscious and thus unable to self-report. Interrater reliability was high in the first two studies, with a weighted kappa coefficient of 0.74 (Payen et al., 2001) and an intraclass correlation coefficient of 0.95 (Aïssaoui et al., 2005), respectively. However, interrater agreement varied from low to high (36% to 91%) in the study by Young, Siffleet, Nikoletti, and Shaw, (2006), where lower agreement was obtained during pain assessments of nociceptive procedures. Discriminant validity was supported in all three studies where higher BPS scores were obtained with nociceptive procedures compared with rest or nonnociceptive procedures. Although feasibility and clinical utility were not formally evaluated, 28 nurses and nurse's aides completed a questionnaire for satisfaction and remarks (Payen et al., 2001). Twenty-four evaluators were satisfied with the instrument's ease of use, and all of them agreed that the assessment required only minimal time (2-5 minutes). Twenty-five felt that effective pain reactions had been assessed, and 26 expected changes in pain management as a result of the BPS (Payen et al., 2001). Seven evaluators expressed concerns regarding complexity of the BPS, although reasons for this were not specified.

Experts strongly recommend that a behavioral pain scale be used to support pain assessment in unconscious or nonverbal critically ill patients (Herr et al., 2006; Jacobi, Fraser, Coursin, Riker, Fontaine, Wittbrodt, et al., 2002). In fact, combining pain assessment with a standardized approach of pain management can lead to better pain control (Chanques, Jaber, Barbotte, Violet, Sebbane, et al., 2006). Knowing this, it is relevant to have access to validated pain tools as well as information about essential clinical characteristics, such as feasibility and clinical utility, to make the best decision about the selection of a tool for implementation into practice. From the available tools for pain assessment in critically ill nonverbal patients, the BPS and the CPOT are recommended in critical reviews (Li et al., 2008; Sessler, Grap, & Ramsay, 2008). Although it is mentioned that further testing is warranted for those two scales, the ambiguity of some of the items of the BPS is highlighted as well as some weaknesses in the validation process and results (e.g., results based on total number of observations rather than individual patients, and reliability results variable). Moreover, feasibility and clinical utility of the BPS have not been described in detail, and little information has been published regarding the methods and instrument used.

Aim 

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The purpose of this study was to describe nurses’ evaluations of the feasibility and clinical utility of the Critical-Care Pain Observation Tool in assessing pain in critically ill ventilated adults.

Methods 

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Design and Sample 

A descriptive design was chosen for this study. It was conducted in the ICU of a university health care center in the Montreal area (Québec, Canada). Patients (n = 55) cared for by the nurse participants during the time of the study were ≥18 years, had a diagnosis of trauma, medical reason (e.g., pulmonary or cardiac problem, hemorrhage, sepsis), or had undergone abdominal or thoracic surgery and were mechanically ventilated. Thirty of them were able to self-report their pain, and the other 25 were unconscious and therefore unable to communicate.

All ICU nurses who had successfully completed their orientation to the unit were invited to participate. A total of 62 nurses agreed to participate and were trained. However, only 51 nurses actually used the CPOT in clinical practice with the patient participants. Of those 51 nurses, 33 completed the evaluation form at the conclusion of the study. It must be noted that two nurses were on maternity leave at the time of the completion of the evaluation form, and two more had left the unit. Considering this, the participation rate was 70%. The study was approved by the Research Ethics Committee of the setting, nurses who participated gave their informed consent, and a signed copy was given to them.

Instruments 

Critical-Care Pain Observation Tool 

The CPOT has been previously published (Gélinas et al., 2006) and includes four behavioral categories: 1) facial expressions; 2) body movements; 3) muscle tension; and 4) compliance with the ventilator for ventilated patients. Each behavior is scored on a scale from 0 to 2 for a possible total score ranging from 0 to 8. The CPOT was initially developed in French and forward-backward translated into English. The English version of the CPOT was used for the present study. Both versions were tested and showed acceptable reliability and validity results (French version: Gélinas et al., 2006; English version: Gélinas & Johnston, 2007).

CPOT Evaluation Form 

The evaluation form, consisting of eight closed-ended questions on a Likert scale response from 1 to 4, was developed by the research team, and inspired from the Puntillo et al. PAIN tool evaluation form (2002) as well as the definitions of feasibility and clinical utility by Duhn and Medves (2004). Length of time to train to use the CPOT accurately, time for assessment and scoring, clarity of directives to use the tool, the tool structure, and the scoring method determined the feasibility. Recommendation of the nurses to use the CPOT routinely, how helpful it is for practice, and how it influenced their practice in assessing the patient's pain determined the clinical utility of the tool. Space for comments or suggestions as well as for reasons supporting their rating of the tool was also provided in the form. At the end, nurses were asked about sociodemographic information (e.g., age, gender), their experience as a nurse, and education level.

Procedure 

Nurse Training 

A convenience sample of 62 ICU nurses who volunteered for the study underwent 1-hour training sessions by the principal investigator to ensure standardization of data collection procedures. The training included the description of the study objectives, the CPOT content (individual indicators), and the scoring method (Appendix), and the data collection sheet. Operational definitions of CPOT indicators, directives for its use, and drawings of facial expressions were provided to the nurses.

Data Collection 

Use of the CPOT tool began when a participating nurse cared for a patient enrolled in the validation study of the CPOT the results of which have been previously published (Gélinas & Johnston, 2007). The CPOT was used with a total of 55 mechanically ventilated adults. The nurses were asked to assess their patient's pain with the CPOT during a nociceptive procedure (turning) and a nonnociceptive procedure (taking noninvasive blood pressure). The CPOT assessments were completed at rest before the procedures, during the procedures, and 20 minutes after the procedures for a total of six assessments per patient. Members of the research team also participated in CPOT assessments and were blinded to the assessments of nurses. A 1-minute observation was required when the patients were observed at rest before and after the procedures, and they were observed for the duration of each procedure to detect any behavior of the patient.

After the completion of CPOT assessments, nurse participants were invited to complete the evaluation form regarding the feasibility and clinical utility of the tool. The questionnaire was sent by internal mail in the clinical setting, and a return envelope was included in the package. Clinicians had a period of 4 weeks to return the questionnaire to the principal investigator. Nurses were identified by a code so that their names were not written on the evaluation form.

Data Analysis 

Descriptive statistics were calculated using SPSS 14.0 to describe the nurse sample and their responses to questions of the evaluation form. Qualitative data were also compiled for comments, suggestions, and rationale of the nurses’ evaluations.

Results 

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Nurse Participants 

Sociodemographic information of nurse participants is described in Table 1. The ICU nurses were aged 24-53 years, with a mean age of 39 years. Most of them were full-time staff nurses and had either a college diploma or a bachelor's degree in nursing. Years of experience in the ICU varied from 6 months to 28 years, with an average of 9 years. Two-thirds of them acknowledged that they had received education in pain in the past at school (college, university), at a conference, or at the hospital.

Table 1.

Description of the Nurses Who Completed the Questionnaire (n = 33)

Variable
Age38.9 ± 9.4
Years of experience as an ICU nurse8.9 ± 8.6
Years of experience as a nurse14.1 ± 9.8
Gender
Female27 (81.8%)
Male6 (18.2%)
Highest education level completed
College diploma (CEGEP)13 (39.4%)
Certificate (university)1 (3%)
Bachelor's degree in nursing18 (54.5%)
Master's degree in nursing1 (3%)
Position in the ICU
Staff nurse28 (84.8%)
Assistant nurse manager4 (12.1%)
Clinical educator1 (3%)
Employee status
Permanent full time28 (84.8%)
Permanent part time5 (15.2%)
Have received education in pain22 (66.7%)

Values are mean ± SD or n (%).

This variable has one missing datum.

CPOT Feasibility and Clinical Utility 

Results from the evaluation form about the feasibility and clinical utility of the CPOT are presented in Table 2, and qualitative comments are described in Table 3. Overall, the feasibility of the CPOT was positively evaluated by the nurse participants. Most questions obtained 90%-100% 3 (sufficiently) and 4 (very) responses, except for question 3 about how quick the CPOT was to use, which reached <80% 3 or 4 responses. Three participants highlighted that the delay between the training and the actual use of the CPOT was too long, and two participants mentioned that the CPOT got quicker to use after getting familiar with it. For a few participants, the CPOT was more difficult to understand regarding choosing the right scoring from the 0 to 2 scale. One participant suggested reducing the number of choices available in the CPOT to make it easier to complete.

Table 2.

Nurses’ Responses to the Questionnaire About the Feasibility and Clinical Utility of the Critical-Care Pain Observation Tool (CPOT)

Frequency (n)
1234
QuestionNot At AllA LittleSufficientlyVery% of Nurses Who Answered 3 or 4
Feasibility
1. Was the length of time sufficient to train to use the CPOT accurately?1223790.9%
2. Were the directives about the use of the CPOT clear?00249100%
3. Is the CPOT quick to use?1220678.8%
4. Is the CPOT simple to understand?002310100%
5. Is the CPOT easy to complete?02161593.9%
Clinical Utility
6. Would you recommend to use the CPOT routinely?27141072.7%
7. Is the CPOT helpful for nursing practice?27141072.7%
8. Has the CPOT influenced your practice in assessing the patient's pain?31111754.5%

This question has one missing datum.

Table 3.

Nurses’ Comments About the Feasibility and Clinical Utility of the Critical-Care Pain Observation Tool (CPOT)

Comment
Frequency
Length of training to use the CPOT
Explanation helped; the use of the CPOT became clearer once done at bedside2
Directives about the use of the CPOT
Delay between the introduction of the study and the actual use of the CPOT was long; review of the directives would help before the first use of the CPOT and before the implementation of the tool into clinical practice3
The CPOT is quick to use
The CPOT got quicker to use after getting familiar with it.2
The CPOT is simple to understand
It was difficult to make out the difference between the choices (scale from 0 to 2) of some indicators of the CPOT (e.g. facial expressions, body movements)2
The CPOT is easy to complete
Fewer choices needed1
Reasons for recommending the use of the CPOT routinely
More uniformity among nurses, common language, organized and standardized way to assess pain in nonverbal patients; helps to validate our observations to the doctors7
It is important to determine pain in critically ill patients and treat it accordingly.4
The CPOT is a good tool to assess pain on a continuous basis in nonverbal patients.3
Other reasons (e.g., for special cases only, to improve our way of providing care)2
Reasons for not recommending the use of the CPOT
Some indicators of the CPOT don't seem to be specific to pain (e.g., agitation, muscle rigidity)2
Extra tool targeting something that is already taken care of by the nurses2
The CPOT is patient selective; cannot be used in patients receiving neuromuscular blocking agents, deeply sedated2
The CPOT is helpful for practice
The CPOT offers a standardized way of assessing pain in nonverbal patients and communicating with the care team9
Assessing and managing pain is an important aspect of practice4
It reminds us to be more aware of how procedures such as turning affect our patient's comfort1
The CPOT is not helpful for practice
Complicated, extra tool, not practical4
Using the CPOT in the study has influenced my practice in assessing the patient's pain
Helps to remind and be more sensitive to nonverbal cues of pain9
Helps to assess pain control2
Advocate for the patient's pain1
Using the CPOT in the study has not influenced my practice in assessing the patient's pain
I've been looking for nonverbal cues of pain before the introduction of the CPOT6
Nothing compares with clinical judgment1

According to its clinical utility, a little more than 70% of the nurses mentioned that the CPOT was helpful for nursing practice and recommended its use routinely. Nurses who recommended its use and mentioned its relevance for nursing practice acknowledged that the CPOT would allow more uniformity among nurses, because it provides common language and a standardized way to assess patients’ pain. The lack of specificity of some indicators of the CPOT and the fact that the tool could not be used with every ICU nonverbal patient were mentioned by nurses who did not recommend its use. Some nurses mentioned that the CPOT was an extra tool which was not necessary, complicated, or not practical to implement in routine care. Half of the nurse participants supported that the CPOT had influenced their practice in assessing the patient's pain. They mentioned that the CPOT helped them to remind and to be more sensitive to nonverbal cues of the presence of pain. For some nurses, the CPOT had not influenced their practice, because they were already sensitive to nonverbal cues of pain before the introduction of the tool. One nurse also highlighted that a tool should not replace clinical judgment.

Discussion 

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The feasibility and clinical utility of the CPOT were examined for the first time in the present study. A high proportion of the nurse participants found the CPOT to be easy to use and relevant for clinical practice. Only 15% of the nurses (5 out of 33) criticized the CPOT as long or complex to use, compared with 36% of the nurses (4 out of 11) who used the PAIN tool (Puntillo et al., 2002) and 25% of those (7 out of 28) who used the BPS (Payen et al., 2001). The CPOT includes only four behavioral indicators, and the PAIN tool is a checklist of 20 items of behavioral and physiologic indicators. And the BPS, even though it includes only three behaviors, they are rated on a 4-point scale in which scores are not clearly described. The ambiguity of some of the BPS items as well as the difficulty in interpreting the tool score have been highlighted in recent critical reviews (Bjoro & Herr, 2008; Li et al., 2008). It has been suggested that the clinical utility of a pain assessment tool can be enhanced by including operational definitions for each indicator and score (Li et al., 2008). The CPOT includes operational definitions, as described in the Appendix.

However, some criticisms of the nurse participants of the CPOT need to be addressed. First, some indicators of the CPOT, such as body movements, may lack specificity to pain. A score of 0 is attributed when the patient is not moving or immobile. However, the absence of movements may not necessarily mean an absence of pain. Indeed, nurses have identified the absence of movements as an indicator of the presence of pain in ICU patients (Puntillo et al., 1997). Remaining immobile may be effective in protecting themselves from pain caused by movements. Also, body movements may vary depending on the patient's level of consciousness or physical factors (e.g., use of physical restraints, medications). For example, it has been reported that the higher the dosage of sedative agents, the lower was the score of a behavioral pain tool (Gélinas & Johnston, 2007; Payen et al., 2001), which makes the CPOT patient selective, as mentioned by two nurses. Unconscious patients are also more likely to exhibit fewer pain behaviors compared with conscious patients (Gélinas & Arbour, in press; Gélinas & Johnston, 2007). Moreover, experts suggest that body movement descriptors would be enhanced by categorizing these responses according to the patient's level of consciousness (Li et al., 2008). In addition, facial expressions seem to differ in head injury patients (Gélinas & Arbour, in press). Further research is warranted in this field to establish the specificity of behavioral parameters as a pain response in ICU patients. In the meantime, it must be emphasized that the CPOT should be used in nonverbal patients who have intact motor function so that they can respond to the tool's requisite behaviors. For instance, the use of the CPOT is not recommended with paralyzed patients and those who are receiving neuromuscular blocking agents. Also, low CPOT scores in heavily sedated patients may not necessarily reflect decreased pain level or the absence of pain in this group and should be interpreted with caution.

It was interesting that some nurses pointed out that they were already sensitive to nonverbal cues of pain before the introduction of the CPOT. This finding is a bit different from the study of Puntillo et al. (2002) 7 years ago with the PAIN tool. With the growing body of knowledge in the field of pain assessment in nonverbal patients in the last decade, nurses have been sensitized to the importance of identifying nonverbal cues of the presence of pain in their practice. Still, for the majority of them, the use of a standardized tool such as the CPOT was helpful. This is consistent with previous studies in which it has been found that the use of a standardized pain documentation tool can lead to better pain assessment (Voight & Paice, 1995) and that combining pain assessment with a standardized approach of pain management can lead to better pain control (Chanques et al., 2006). Knowing this, it is urgent that clinical guidelines and recommendations in pain assessment and management be implemented into practice (Jacobi et al., 2002; Herr et al., 2006).

Even if the use of behavioral scales is known as a valid approach to pain assessment, it must be emphasized that they are not always accurate reflections of pain intensity. Experts underscore that behavioral scores should not be interpreted as pain intensity scores nor compared with standard categories of pain levels (mild, moderate, severe). Results from a previous study also support this statement. Indeed, the CPOT was found to adequately classify postoperative ICU patients with severe pain but not those with mild or moderate pain (Gélinas et al., 2009). Thus, a behavioral score may be helpful in identifying the presence of pain (rather than rating pain intensity) and in evaluating interventions for pain management (Herr et al., 2006).

Limitations 

This study was not without limitations. First, the sample size was small and the participation rate was moderate. Of the nurses who did not return their completed evaluation form (n = 14), eleven of them had assessed only one (n = 9) or two (n = 2) patients with the CPOT. They may not have felt that they had enough exposure to the CPOT to evaluate its clinical characteristics. Second, nurse participants were provided only with paper documents for the CPOT training. Other educational material, such as patients’ videotapes, would have enhanced the training and would have allowed evaluating the nurses’ skills in using the tool. Third, the CPOT was used for research purposes in this study, so that nurse participants used it for enrolled patients only. Of note, the range of patients evaluated by the nurse participants varied from one to eight patients per nurse. This wide range of exposure to the use of the CPOT may have influenced the study findings.

Future Directions 

A study is being conducted by Desjardins, Gélinas, and colleagues about the implementation of the CPOT in the ICU of a university health care center near the Montreal area (Quebec, Canada). Training of the nurses has been enhanced with patients’ videotapes, a CPOT pocket tool, posters of the CPOT and directives of its use in the ICU, and evaluations of the nurse's skills in using the CPOT. All ICU patients unable to self-report their pain with intact motor function and not receiving neuromuscular blocking agents are eligible for the CPOT. The impact of the implementation of the CPOT into practice will be evaluated with chart audits before the CPOT was introduced and 3 months and 12 months after its implementation. Nurses’ evaluations of the feasibility and clinical utility of the tool will be examined as well. That study will provide results of these characteristics based on clinical purposes.

Conclusions 

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So far, the CPOT has demonstrated acceptable results of reliability and validity in both conscious and unconscious ICU adults. Its feasibility and clinical utility have also been positively evaluated by ICU nurses who used it for the purpose of research. The use of a valid behavioral pain scale is recommended in clinical guidelines for pain assessment in nonverbal patients (Herr et al., 2006), and the CPOT is suggested by many experts in critical reviews (Li et al., 2008; Sessler et al., 2008). At this point, the CPOT is being used for either research or clinical purposes in many health care centers in Canada, the United States, and other countries. It is available in French and English, and translations in other languages are in progress (i.e., Finnish, Portuguese, Italian, and Swedish). Even if further research is warranted to improve the specificity of some indicators of the CPOT and to evaluate its feasibility and clinical utility in routine care, the CPOT appears to support ICU nurses in the assessment of their patients’ pain and could contribute to better pain control in the critically ill adult.

Acknowledgement 

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The author thanks Lindsay Hammond, master's degree student in nursing at McGill University, for her work in updating the literature review.

Appendix 

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Description and Directives to Use the Critical-Care Pain Observation Tool (CPOT)

Indicator
Score
Operational definition
Facial expressionsRelaxed, neutral0No muscle tension observed
Tense1Presence of frowning, brow lowering, orbit tightening, and levator contraction or any other change (e.g., opening eyes or tearing during nociceptive procedures)
Grimacing2All previous facial movements plus eyelid tightly closed (the patient may present with mouth open or biting the endotracheal tube)

Body movementsAbsence of movements or normal position0Does not move at all (doesn't necessarily mean absence of pain) or normal position (movements not aimed toward the pain site or not made for the purpose of protection)
Protection1Slow, cautious movements, touching or rubbing the pain site, seeking attention through movements
Restlessness2Pulling tube, attempting to sit up, moving limbs/thrashing, not following commands, striking at staff, trying to climb out of bed

Compliance with the ventilator (intubated patients)Tolerating ventilator or movement0Alarms not activated, easy ventilation
Coughing but tolerating1Coughing, alarms may be activated but stop spontaneously
Fighting ventilator2Asynchrony: blocking ventilation, alarms frequently activated
OR
Vocalization (extubated patients)Talking in normal tone or no sound0Talking in normal tone or no sound
Sighing, moaning1Sighing, moaning
Crying out, sobbing2Crying out, sobbing

Muscle tension: Evaluation by passive flexion and extension of upper limbs when patient is at rest or evaluation when patient is being turnedRelaxed0No resistance to passive movements
Tense, rigid1Resistance to passive movements
Very tense or rigid2Strong resistance to passive movements, incapacity to complete them
TOTAL — / 8

Adapted with permission From Gélinas et al., (2006).

Directives to Use the CPOT 


1.The patient must be observed at rest for 1 minute to obtain a baseline value of the CPOT.

2.Then the patient should be observed during nociceptive procedures (e.g., turning, endotracheal suctioning, wound dressing) to detect any changes in the patient's behaviors in response to pain.

3.The patient should be evaluated before and at the peak effect of an analgesic agent to assess if the treatment was effective in relieving pain.

4.For the rating of the CPOT, the patient should be attributed the highest score observed during the observation period.

5.The patient should be attributed a score for each behavior included in the CPOT, and muscle tension should be evaluated last, especially when the patient is at rest, because just the stimulation of touch (passive flexion and extension of the arm) may lead to behavioral reactions.

Facial Expressions 


0:Relaxed, neutral (no muscle tension)

1∗:Tense (frowning, brow lowering, orbit tightening, little levator contraction)

2:Grimacing (contraction of the whole face: frowning, brow lowering, eyes tightly closed, levator contraction; mouth may be opened or the patient may be biting the endotracheal tube)

∗A score of 1 may be attributed when a change in the patient's facial expression is observed compared with rest assessment (e.g., open eyes, weeping eyes).

Drawings by Caroline Arbour, RN, BSc, MScA(c), McGill University.

The drawings were inspired from: Prkachin, K. M. (1992). The consistency of facial expressions of pain: A comparison across modalities. Pain, 51, 297-306.

References 

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School of Nursing, McGill University, Montréal, Québec, Canada and the Centre for Nursing Research, Jewish General Hospital

Corresponding Author InformationAddress correspondence to Céline Gélinas, RN, PhD, Assistant Professor, School of Nursing, McGill University, 3506, University Street, Wilson Hall, Room 420, Montreal, Quebec, H3A 2A7 Canada.

 Supported by a Research Development Grant from the Jewish General Hospital Foundation.

PII: S1524-9042(09)00053-8

doi:10.1016/j.pmn.2009.05.002


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