One of the important activities nursing is the alleviating of discomfort including pain as providing comfort to patient. Postoperativediscom has been underestimated because it is only a part of postoperative physiological process and disappear in time. The study was designed to investigate the effect of relaxation technique on postoperative discomfort of patients with lumbosacral back pain. A total of 40 patients were selected as a subject from August 12th to October 10th 1995 who had been hospitalized at NS and OS nursing units in K medical center. Of them twenty were in the experimental group and the remaining twenty were in the control group in convenience sampling. The tools for study were Relaxation technique, designed to use postoperative setting adequately by Park, and Postoperative Discomfort Scale. The data were analyzed by use of t-test an x2 test. The study was concluded as follows : The main hypothesis, that "the experimental group who used relaxation technique will express a lesser score of postoperative discomfort than the control group who did not use relaxation technique" is divided into seven sub-hypotheses. Hypothesis 1, that "the experimental group will express less postoperative pain than the control group"was supported(t=-7.52, p=0.000). Hypothesis 2, that "the experimental group will express less postoperative feeling of unpleasantness than the control group"was supported(t=-7.04, p=0.000). Hypothesis 3, that "the experimental group will express less postoperative immobilization discomfort than the control group"was supported(t=-6.66, p=0.000). Hypothesis 4, that "the experimental group will show fewer nonverbal expressions of postoperative distress than the control group"was supported(t=-3.75, p=0.01). Hypothesis 5, that "the experimental group will use analgesic medication less frequently than the control group" was supported(t=-4.15, p=0.000). Hypothesis 6, that "the experimental group will have less change in vital sings between the pre and postoperative periods than control group"was supported only for respiratory rate(t=-4.06, p=0.000). Hypothesis 7. that "the experimental group will express less postoperative voiding difficulty than the control group"was not supported(t=0.06, p=0.951). As a result, this study showed that relaxation technique has the effect to postoperative discomfort of the patients with lumbosacral back pain, so the researcher thought it is enable for nurses to help patients undergoing postoperative discomfort.
Back Pain* ; Humans ; Immobilization ; Nursing ; Pain, Postoperative ; Physiological Processes ; Postoperative Period ; Relaxation*

This study was designed to evaluate whether the nurses' assessment of postoperative pain can be an alternative to patients' self-reporting. We examined 187 patients receiving postoperative intravenous patient-controlled analgesia. The nurses assessed the patients' pain with three pain indices (therapeutic efficacy, pain intensity, and facial pain expression) 8 hr after operation. The patients recorded their resting and movement pain using 100-mm visual analog scales immediately following the nurses' assessment. There was an acceptable correlation between overall pain measurement assessed by patients and that assessed by nurses (canonical correlation coefficient=0.72, p=0.0001). The resting pain was more reliably reflected than the movement pain in overall measurement assessed both by nurses and by patients. Among the three pain indices assessed by nurses, the pain intensity most reliably reflected the patients' self-reports. The pain intensity assessed with a simple verbal descriptor scale therefore is believed to be an effective alternative to the patients' self-reports of postoperative pain at rest. However, it mirrored the patients' self-reports during movement less reliably. Therapeutic efficacy and facial pain expression indices were not effective alternatives to patients' self-reporting.
Analgesia, Patient-Controlled ; Facial Expression ; Human ; Nursing Assessment/*methods/standards ; Pain Measurement ; Pain, Postoperative/*nursing ; Perioperative Nursing/*methods ; Reproducibility of Results

PURPOSE: The purpose of this study was to evaluate the effects of preoperative pain control education on the pain control barrier, postoperative pain and pain control satisfaction in gynecological patients. METHOD: The study was a quasi-experimental research design. There were 58 subjects who were admitted for gynecological surgery to D University Hospital in B city. Pain control education was provided individually to the experimental group one day before their operation day for 20 minutes with the 'Pain Control Guide Book' in the patient's admission room. The education book was made by researchers based on pain management references and patient interviews. For assessing the pain control barrier, a simplified version of Barriers Questionnaire was used, postoperative pain was assessed on a numeric scale(0-10) and satisfaction of pain control was assessed by one question. RESULTS: The pain control barrier(F=15.828, p<.001) and the post pain score of the experimental group was lower than that of the control group. In addition, pain control satisfaction of the experimental group(t=3.612, p<.001) was higher than the control group's. CONCLUSION: With the above results, preoperative pain control education could be an effective nursing intervention for pain control of surgical patients.
Adult ; Aged ; Female ; Genital Diseases, Female/*nursing/pathology ; Humans ; Middle Aged ; Pain/nursing/*prevention & control ; Pain, Postoperative/nursing/*prevention & control ; *Patient Education as Topic ; Patient Satisfaction ; Preoperative Care/nursing

The purpose of this study was to evaluate the effect of informational intervention on postoperative pain following tonsillectomy in children. This study was performed on 30 children, aged 5-15 years, undergoing tonsillectomy and their parents by providing informational intervention with colored figure; operation procedure and information. Pain assessment was done by Pain Questionnaire. The results from this study were as follows : 1. Children in experimental group with mean 16.07 had lower pain scores than control group with mean 14.87 at 4th hours after operation(p < 0.05). It showed "significant difference" and first hypothesis was adopted. 2. Children in experimental group with mean 20.60 had lower pain scores than control group with mean 17.27 at 8th hours after operation(p < 0.05). It showed "significant difference" and second hypothesis was adopted. 3. Children in experimental group with mean 28.80 had lower pain scores than control group with mean 25.70 at 24th hours after operation(p < 0.05). It showed "significant difference" and third hypothesis was adopted. 4. When we analyzed the time difference and difference between two groups simultaneously by repeated measure ANOVA, the significant difference was not found. And so "the experiential group with operation-related information will show the lower pain sense than the control group just as the time flows after operation", fourth hypothesis was rejected. Generally, it was found that providing information about operation to children and their parents reduced effectively postoperative pain in children, but in clinical settings there are minimum preoperative information-providing because of insufficient time and inconvenience although nursing staffs and patients know its needs. Conclusionally providing preoperative information should help children and their parents cope with Pre, Peri and Post operative events effectively.
Adenoidectomy ; Analysis of Variance ; Child* ; Humans ; Methods ; Nursing Staff ; Pain Measurement ; Pain, Postoperative* ; Parents ; Tonsillectomy* ; Child Health

PURPOSE: The purpose of this study was to identify pain intensity according to activities over postoperative days and to identify factors of patient satisfaction with pain management after abdominal surgery. METHODS: The subjects were 123 patients who were admitted at a general surgical ward and had abdominal surgery from Mar. 2005 to June 2005. The collected data were analyzed using the SPSS 12.0 program. RESULTS: The average postoperative pain scores were 6.13 at POD 1, 5.46 at POD 2, and 4.22 at POD 3. In stepwise multiple regression analysis a total of 40% of variance in satisfaction with pain management was accounted for by pain intensity on POD 3 at rest (29.4%) and attitude toward using pain medicine (6.6%), and side effects of pain medicine (4.0%). CONCLUSION: According to the findings of this study, patients had inadequate pain management after abdominal surgery. Therefore, nurses need to provide educational programs focused on changing attitudes toward using pain medicine, to reduce side effects of pain medicine, and to develop nursing intervention for relieving pain.
Analgesia, Patient-Controlled ; Humans ; Nursing ; Pain Management ; Pain, Postoperative* ; Patient Satisfaction

PURPOSE: The purpose of the study was to test the effects of music therapy on postoperative pain in patients with total hip replacement. METHOD: The research design was a nonequivalent control group pretest-posttest design. The subjects were composed of thirty patients with total hip replacement. Fifteen of them were assigned to the experimental group and fifteen to the control group. Fifteen minutes tailored music therapy was given to the experimental group during five consecutive days. The instruments used for this study were pain NRS(numerical rating scale). The data were analyzed using percent, mean, standard deviation, chi-square-test and repeated measure ANOVA using SPSS WIN 11.0. RESULTS: Hypothesis 1 "The score of pain NRS of experimental group will be lower than those of control group" was accepted(F=15.945, p<.001). Hypothesis 2 "The frequency of PCA analgesics of experimental group will be fewer than those of control group" was accepted (t=-2.312, p=.028). Hypothesis 3 "The vital signs(pulse, systolic BP and diastolic BP) of experimental group will be different from those of control group" was rejected. CONCLUSION: This music therapy can be recommended as an efficient nursing intervention to reduce postoperative pain in patients with total hip replacement.
Analgesics ; Arthroplasty, Replacement, Hip* ; Humans ; Music Therapy* ; Music* ; Nursing ; Pain, Postoperative* ; Passive Cutaneous Anaphylaxis ; Research Design

BACKGROUND: The objects of this study were to determine the effects of foot reflexo massage on the postoperative pain of the subtotal gastrectomy patients according to quasi-experimental research design, and to provide demonstrative data for using the foot reflexo massage as an intervention for pain nursing. METHODS: The foot reflexo massages were performed on 34 subtotal gastrectomy patients after informed consent was obtained. They were divided into two groups, i.e. control group (n=17) and experimental group (n=17). After 6 hours and 12 hours from the subtotal gastrectomy, the massage was carried out on each foot for 10 minutes twice. Visual analogue scale (VAS) was employed as the measurement tools of pain, and the degree of postoperative pain was measured through frequency of prn (pro re nata) analgesia in chart review. RESULTS: The experimental group with foot reflexo massage 6 hours after the operation have significantly less score of postoperative pain than the control group (5.76+/-0.83, 4.35+/-1.0, p=.000). The experimental group with foot reflexo massage 12 hours after the operation have significantly less score of postoperative pain than the control group (5.12+/-0.53, 3.00+/-1.17, p=.000). The experimental group with foot reflexo massage have significantly less frequency of prn analgesics than the control group from six hours to twelve hours after the operation (p=.004). CONCLUSIONS: It is considered foot reflexo massage is effective for reducing postoperative pain of subtotal gastrectomy patients, as well as useful for an immediate nursing intervention.
Analgesia ; Analgesics ; Foot* ; Gastrectomy* ; Humans ; Informed Consent ; Massage* ; Nursing ; Pain, Postoperative* ; Research Design

PURPOSE: This study was to identify knowledge, attitude, use and state of the Patient Controlled Analgesics (PCA) in postoperative patients. METHOD: The research design was a descriptive research. From December 7, 2005 to January 6, 2006, 102 postoperative patients in a university hospital at Daegu were participated in the study. RESULTS: Analgesics with PCA were mainly morphine complex 73.5% and Demerol complex 26.5%. Previous experience of using PCA was only 28.4%, and the main sources of information were other post-op patients and families(43.1%). The most common reason of choice was a recommendation from other post-op patients and families(46.1%). The most common side effects of PCA were nausea and vomiting(20.6%). About 57% of the patients were satisfied with PCA, and pain scores decreased with PCA. Mean score for knowledge about PCA was 2.55 out of a possible 6, and for attitude related to pain medication. 2.31 out of possible 5. CONCLUSION: To increase the score on knowledge of PCA, a structured preoperative PCA education program should be developed by nursing staff.
Analgesics ; Daegu ; Education ; Humans ; Meperidine ; Morphine ; Nausea ; Nursing Staff ; Pain, Postoperative ; Passive Cutaneous Anaphylaxis ; Research Design

Postoperative pain is a major problem that may restrict early mobilization and hospital discharge of surgical patients and it may cause psychologic trauma in pediatric patients, so effective postoperative analgesia is important especially in pediatric surgery. A study was undertaken to test the effect of intraoperative wound irrigation with bupivacaine for postoperative analgesia in pediatric inguinoscrotal surgery and the analgesic effect was measured with postoperative analgesics requirement and pain score. A total of 149 patients of 5 months to 13 years old were enrolled in our study. In comparison of analgesics requirement a total of 69 patients were enrolled and assigned to 2 groups. Group 1 was treated with wound irrigation with 0.21 ml/kg 0.25 % bupivacaine solution before closure of the inguinal canal and before suturing the subcutaneous layer. Group 2 was treated with normal saline instead of bupivacaine. Postoperatively 3 mg/kg phenobarbital was administered intramuscularly on complaint of pain. And the total number of doses of phenobarbital administered during first 24 hours of postoperative period was recorded. Drug administration and patient evaluation were double-blinded. In comparison of pain score a total of 80 patients were enrolled and assigned to 2 groups as same method as above and score according to the Oucher pain scale was recorded by nursing staff to assess the efficacy of intraoperative bupivacaine irrigation. The children in the bupivacaine group required significantly less postoperative medication for analgesia than those in the control group. The average number of doses of phenobarbital in the bupivacaine group was 0.189 +/- 0.065 compared to 0.594 +/- 0.109 in the control group (p=0.002). On the Oucher pain scale the bupivacaine group reported less pain than the control group (score 27.69 +/- 6.04 versus 37.56 +/- 5.18, respectively, p=0.01). We concluded that bupivacaine irrigation effectively decreases postoperative pain and narcotic drug requirement, and the irrigation of wounds with bupivacaine should be a routine procedure in elective inguinoscrotal surgery in children.
Adolescent ; Analgesia* ; Analgesics ; Bupivacaine* ; Child* ; Early Ambulation ; Humans ; Inguinal Canal ; Nursing Staff ; Pain, Postoperative ; Phenobarbital ; Postoperative Period ; Wounds and Injuries

PURPOSE: The purpose of this study was to develop evidence-based guidelines on postoperative pain management via the web and to examine the effects in terms of pain level of patients undergoing abdominal surgery and nurses' knowledge of postoperative pain management. METHODS: First, evidence-based pain guidelines were developed via the web in a tertiary hospital. Second, a special educational program on evidence-based pain guidelines for nurses was developed after validation of content by experts. Third, diverse strategies were adopted in order to facilitate incorporation of evidence-based pain guidelines in practice. Fourth, nurses in the study units were educated on evidence-based guidelines using the developed educational program for 3 weeks before their implementation of evidence-based pain guidelines to patients. Patients were assigned to the control group (from July 29 to August 20, 2011) and the experimental group (from September 24 to October 25, 2011) according to interrupted time interval. The data were analyzed using chi-square test, analysis of variance test with Scheffes test as a post hoc and repeated measure of analysis of variance. RESULTS: Patients in the experimental group showed a significantly lower level of pain. Nurses' knowledge of management of postoperative pain showed a significant increase after installation of evidence-based guidelines. CONCLUSION: Evidence-based pain guidelines were effective in reducing the pain level of patients as well as improving nurses' knowledge of pain management.
Abdomen/surgery ; Adult ; Case-Control Studies ; Education, Nursing, Continuing/*methods ; *Evidence-Based Nursing ; Female ; Guidelines as Topic ; *Health Knowledge, Attitudes, Practice ; Humans ; *Internet ; Male ; Pain Management/*nursing ; Pain, Postoperative/*nursing ; Republic of Korea ; Treatment Outcome ; Young Adult