Skip to main content

Armbruster, S.D., Song, J., Gatus, L., Lu, K.H., & Basen-Engquist, K.M. (2018). Endometrial cancer survivors' sleep patterns before and after a physical activity intervention: A retrospective cohort analysis. Gynecologic Oncology, 149, 133–139.

Study Purpose

To determine baseline sleep characteristics of endometrial cancer survivors, the impact of demographic and treatment characteristics on sleep quality, the association of sleep quality with quality of life and stress levels, and the impact of physical activities on sleep.

Intervention Characteristics/Basic Study Process

Individualized exercise prescriptions based on baseline function. Adherence to the American College of Sports Medicine Guidelines requiring 30 minutes of moderate exercise five or more days per week or at least 20 minutes of rigorous exercise three or more days per week with telephone-based counseling sessions, printed materials, and pedometers. Decreasing frequency of counseling telephone calls from weekly to twice monthly to monthly over six months.

Sample Characteristics

  • N = 95   
  • AGE: 57.1 years (range = 25-76)
  • FEMALES: 100%
  • CURRENT TREATMENT: Radiation, other
  • KEY DISEASE CHARACTERISTICS: 76% stage I

Setting

  • SITE: Single site   
  • SETTING TYPE: Outpatient    
  • LOCATION: Houston, TX

Phase of Care and Clinical Applications

  • PHASE OF CARE: Transition phase after active treatment
  • APPLICATIONS: Elder care 

Study Design

Secondary analysis of Steps to Health, a single-arm cohort study.

Measurement Instruments/Methods

Sleep quality measured with the Pittsburgh Sleep Quality Index (PSQI). Physical activity measured with the Community Health Activities Model Program for Seniors (CHAMPS). Quality of life (QOL) measured with the SF-36.

Results

At baseline, 61% of the sample had poor sleep quality (PSQI > 5). Obese survivors were more likely to have sleep disturbances than were their normal-weight counterparts (p = 0.029). At baseline, poor sleepers had higher stress levels than good sleepers (p = 0.002). Poor sleep quality was associated with lower health-related QOL: vitality (p = 0.001), bodily pain (p = 0.004), general health (p = 0.002), social functioning (p = 0.005), role limitations caused by emotional problems (p = 0.005), mental health (p = 0.002), and the mental component score (p = 0.003). Sleep quality improved in cancer survivors who increased their weekly total physical activity or moderate-vigorous intensity physical activities (MPVA) throughout the intervention (p = 0.004 and 0.05, respectively). Adjusting for covariates (e.g., age, time since diagnosis, obesity status, disease stage, treatment), improvement in sleep quality was associated with increased hours of total activity (p = 0.026).

Conclusions

Poor sleep quality was common in endometrial cancer survivors and an increase in physical activity was associated with improved sleep quality.

Limitations

  • Small sample (< 100)
  • Risk of bias (no control group)

Nursing Implications

Sleep problems are common in women following treatment for endometrial cancer and are associated with stress and poor QOL. Increasing physical activity may improve sleep quality for these women.

Print

Özkaraman, A., Dugum, O., Ozen Yilmaz, H., & Usta Yesilbalkan, O. (2018). Aromatherapy: The effect of lavender on anxiety and sleep quality in patients treated with chemotherapy. Clinical Journal of Oncology Nursing, 22, 203–210.

Study Purpose

To determine the effects of lavender oil aromatherapy on anxiety and sleep quality in patients undergoing paclitaxel-based chemotherapy.

Intervention Characteristics/Basic Study Process

Patients were randomized to lavender essential oil (Lavandula hybrid), tea tree oil, or control. During the first chemotherapy infusion, three drops of lavender essential oil or tea tree oil were put onto a piece of cotton that was placed on each patient’s neck and shoulders, about 10 inches below the nose. No aromatherapy was administered to the control group. Patients randomized to lavender and tea tree oils continued to smell the oil for five minutes every night for one month. Lavender and tea tree oil were purchased from a herbal product firm with quality certifications. Tea tree oil does not have a sedative or relaxing effect; therefore, it was used as a placebo. Patients were evaluated at baseline, after the first chemotherapy infusion, and after one month of chemotherapy infusions.

Sample Characteristics

  • N = 70    
  • MEAN AGE: 58.22 years
  • MALES: 16%  
  • FEMALES: 84%
  • CURRENT TREATMENT: Chemotherapy
  • KEY DISEASE CHARACTERISTICS: Mixed cancers; 66% breast cancer, 16% lung cancer, 18% other cancers
  • OTHER KEY SAMPLE CHARACTERISTICS: All chemotherapy regimens included weekly paclitaxel

Setting

  • SITE: It appears that the data was collected at a single site, but this is not clearly stated.      
  • SETTING TYPE: Outpatient
  • LOCATION: Private hospital in Turkey

Phase of Care and Clinical Applications

  • PHASE OF CARE: Active anti-tumor treatment
  • APPLICATIONS: Not available

Study Design

Randomized control trial with three arms (lavender oil, tea tree oil, control)

Measurement Instruments/Methods

Pittsburgh Sleep Quality Index (PSQI), State-Trait Anxiety Inventory (STAI), measured before and after chemotherapy treatment

Results

A significant improvement in sleep quality as measured by mean score of PSQI before and after chemotherapy in the lavender group (time, p = 0.001), with group differences between lavender and the other groups based on assessments (group*time, p = 0.001). Trait anxiety values before and after chemotherapy were significantly decreased in the lavender group (p = 0.0003); however, there was no difference state anxiety by time or group.

Conclusions

Lavender oil inhalation at bedtime for outpatients with mixed cancer treated with paclitaxel-based chemotherapy may be useful for improving sleep quality and trait anxiety.

Limitations

  • Small sample (< 100)
  • Risk of bias (no blinding)
  • Findings not generalizable
  • Other limitations/explanation: Small study arms (n = 30, 20, and 20), non-blinded participants because most people are familiar with lavender scent, lack of data analysis details–difficult to understand results.

Nursing Implications

Lavender oil inhaled at bedtime appears to be an acceptable and helpful intervention for adults treated with paclitaxel-based chemotherapy for mixed cancer types with poor sleep quality and medium levels of state and trait anxiety. Additional research in larger samples is warranted before recommending for practice in general oncology populations.

Print

Blackburn, L., Achor, S., Allen, B., Bauchmire, N., Dunnington, D., Klisovic, R. B., . . . Chipps, E. (2017). The effect of aromatherapy on insomnia and other common symptoms among patients with acute leukemia. Oncology Nursing Forum, 44, E185–E193.

Study Purpose

To determine if aromatherapy by diffusion of essential oils improves insomnia in hospitalized patients with newly diagnosed acute leukemia undergoing induction chemotherapy.

Intervention Characteristics/Basic Study Process

Patients served as their own controls and were randomized to receive aromatherapy over 3 weeks in the following fashion. 1 week placebo or aromatherapy, followed by a 1 week washout period, and a third week of placebo or aromatherapy. Patients were allowed to choose their preferred essential oil for the aromatherapy, lavender, chamomile, or peppermint.  Rose water served as the placebo control.  The aromatherapy diffuser was placed in the same location in all hospital rooms. 8 blinded drops of placebo or essential oil were placed in a diffuser each evening at 9 pm and ran until drops were gone (approx. 8 hours). Sleep quality and disturbance were measured at baseline and after each week of the intervention (placebo or aromatherapy), a general symptom assessment was completed daily during the intervention weeks, and the evaluation of aromatherapy was completed at the end of each week of the intervention.

Sample Characteristics

  • N = 50    
  • AGE: 19-72 yrs
  • MALES: 56%  
  • FEMALES: 44%
  • CURRENT TREATMENT: Chemotherapy
  • KEY DISEASE CHARACTERISTICS: Newly diagnosed patients with acute leukemia
  • OTHER KEY SAMPLE CHARACTERISTICS: initiating 4 weeks of induction chemotherapy

Setting

  • SITE: Single site   
  • SETTING TYPE: Inpatient    
  • LOCATION: Midwestern university medical center

Phase of Care and Clinical Applications

PHASE OF CARE: Active antitumor treatment

Study Design

Randomized control trial.  Trial was a crossover over trial with a washout period in which patients served as own control.

Measurement Instruments/Methods

Pittsburgh Sleep Quality Index (PSQI), Edmonton Symptom Assessment Scale-Revised (ESASr), Final evaluation of aromatherapy (FEA)

Results

Sleep quality as measured by mean scores on the PSQI improved with aromatherapy (p=0.0001) with specific improvements in sleep duration (p=0.03),  sleep quality (p=0.05), and sleep disturbance (p=0.04).  General symptom scores as measured by the EASSr , all subscales, improved with aromatherapy treatment (p=0.0006)

Conclusions

Aromatherapy for hospitalized patients with acute leukemia undergoing induction chemotherapy improves sleep disturbances and other symptoms.

Limitations

  • Small sample (< 100)
  • Findings not generalizable
  • Other limitations/explanation:  Participants were allowed to choose their own oil, may have biased results?  Were nurses really blinded to the assignment?  FEA form used for evaluation of aromatherapy is an investigator developed tool that has no reliability or validity data.

Nursing Implications

Aromatherapy appears to be an effective intervention for improving sleep wake disturbances and other symptoms in hospitalized patients with acute leukemia.  Nurses may want to explore ways to use aromatherapy for patients in their institutions as well as educate patients and families about the potential positive benefits of aromatherapy as a non-pharmacological method to treat sleep wake disturbances as well as a variety of other symptoms.

Print

Longo, M.A., Cavalheiro, B.T., & de Oliveira Filho, G.R. (2018). Systematic review and meta-analyses of tranexamic acid use for bleeding reduction in prostate surgery. Journal of Clinical Anesthesia, 48, 32–38.

Purpose

The purpose of the systematic review and meta-analysis was to identify if there is a difference between tranexamic acid (TXA) and a control group in blood loss, transfusion rates, hemoglobin levels, and thromboembolic events in prostate surgery patients.

Search Strategy

  • TYPE OF STUDY: Meta analysis and systematic review
  • DATABASES USED: Medline, Cochrane Central Register of Controlled Trials, EBSCO, and Web of Science
  • YEARS INCLUDED: 1976,1980, 2004, 2011, 2016, 2017
  • INCLUSION CRITERIA: Randomized controlled trials comparing use of TXA with a control group
  • EXCLUSION CRITERIA: None stated

Literature Evaluated

  • TOTAL REFERENCES RETRIEVED: 145
  • EVALUATION METHOD AND COMMENTS ON LITERATURE USED: Grading of Recommendations Assessment, Development, and Evaluation methodology was used for evaluation

Sample Characteristics

  • FINAL NUMBER STUDIES INCLUDED: 9 
  • TOTAL PATIENTS INCLUDED IN REVIEW: 978 
  • SAMPLE RANGE ACROSS STUDIES: 494 received TXA and 484 enrolled in the control group
  • KEY SAMPLE CHARACTERISTICS: TXA was administered via IV in six of the studies, orally in two, and local spray in one.

Phase of Care and Clinical Applications

PHASE OF CARE: Diagnostic

Results

The results were reported on nine studies. Of the nine studies, six reported on the interoperative blood loss showing overall blood loss was lower in the TXA group (p < 0.000001). Transfusion rate was identified less in the TXA group (p < 0.00004) in six of the nine studies with the prostatectomy cases but not the TURP cases. Hemoglobin level was monitored 24 hours after surgery, but there was no noted significant difference between the TXA and the control groups in four of the studies. Eight studies monitored for DVT and PE, and no statistical difference was found.

Conclusions

This systemic review and meta-analyses concluded that patients who received TXA treatment during prostate surgery had a reduction in interoperative blood loss and decrease need for transfusion with no increased risk of DVT or PE.

Limitations

  • Limited number of studies included
  • High heterogeneity

Nursing Implications

Although there was no increase in risk for DVT or PE using TXA, nurses should still be aware of the potential risk and monitor the patient with discretion.

Print
Subscribe to