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. Author manuscript; available in PMC: 2013 Jul 30.
Published in final edited form as: J Appl Gerontol. 2012 Mar 22;32(4):443–456. doi: 10.1177/0733464811432632

Functional Outcomes by Age for Inpatient Cancer Rehabilitation: A Retrospective Chart Review

Elizabeth G Hunter 1, Julie Baltisberger 2
PMCID: PMC3727991  NIHMSID: NIHMS450810  PMID: 23908563

Abstract

Cancer-related impairments result in disabilities similar to those typically encountered in inpatient rehabilitation settings; however, the use of rehabilitation services by cancer survivors is low. This is particularly important for older adults as they are at higher risk for cancer. This retrospective study collected data from medical records from 215 charts of patients admitted to an inpatient physical rehabilitation hospital, within a 5-year period, with a primary diagnosis of cancer. Mean age was 61 years (SD = 15.7) for 109 (51%) females and 106 (49%) males. Regardless of age, patients achieved significant functional improvement, as shown by their FIM scores (t = 23.06, p < .0001), from admission to discharge. The results have several important implications related to cancer survivorship among older adults. With a push toward aging in place, maintaining optimal physical functioning is crucial. Physical rehabilitation benefited the functional outcomes of this group of cancer survivors regardless of age.

Keywords: cancer rehabilitation, comorbidities, rehabilitation outcomes, aging, cancer survivorship


Cancer has been called the disease of elderly people; advancing age is associated with an increased risk of cancer (Ershler, 2003). By 2030, the number of Americans aged 65 or above is expected to reach 71 million (Center for Disease Control and Prevention, 2007). Nearly 60% of cancer diagnoses and 70% of cancer deaths occur in individuals aged 65 or above (Ries et al., 2007). The incidence of cancer in older adults is expected to multiply, so that by 2030, approximately 70% of all cancer diagnoses will be for older adults (Smith, Smith, Hurria, Hortobagyi, & Buchholz, 2009). Despite the disproportionate burden of cancer among older adults, when compared with younger adults, older adults experience multiple disparities in cancer care. For example, they are treated less aggressively (Schrag, Cramer, Bach, & Begg, 2001). Although older cancer survivors suffer losses in all functional domains, the most profound are in the area of physical functioning (Demark-Wahnefried, Morey, Sloane, Snyder, & Cohen, 2009). In 1996, the National Cancer Institute (NCI) established the Office of Cancer Survivorship with a mission to improve the length and quality of life of all people diagnosed with cancer (NCI website). The direct effects of cancer and its treatment often result in physical impairments that can substantially decrease quality of life (Marciniak, Sliwa, Spill, Heinemann, & Semik, 1996). Although cancer related impairments result in disabilities similar to those frequently encountered in inpatient rehabilitation settings, the use of rehabilitation services by cancer survivors is low (Cheville, Troxel, Basford, & Kornblith, 2008; Movsas et al., 2003, Vargo, 2008; Warfel, Lachmann, & Nagler, 1993). The low utilization of services is clearly associated with a lack of effective systems for recognizing the need for rehabilitation (Vargo, 2008).

Many cancer survivors report declines in their physical functioning, including basic body mobility and engagement in work and leisure activities (Kroenkeet al., 2004; Nomori, Watanabe, Ohtsuka, Naruke, & Suemasu, 2004). Across cancer diagnoses and types of treatment, adult survivors report that they have not fully regained their precancer levels of physical functioning or engagement in social, work, or leisure activities (Fialka-Moser, Crevenna, Korpan, & Quittan, 2003; Ganz et al., 2003; Lehmann et al., 1978). Treating older adults with cancer requires the ability to differentiate between the influences of aging, comorbidities, and the acute and late effects of cancer and cancer treatment (Bond, 2010). Age-related physiological changes not only contribute to the development of cancer in older adults but also affect treatment tolerance and response (Bond, 2010).

Providers do not often offer rehabilitation services for a cancer diagnosis, even though these services seem to be a viable opportunity to optimize functional restoration (Feuerstein, 2009). Lack of referral to physical rehabilitation combined with age and possible multiple comorbidities may combine to foster lower quality of life and functional outcomes for cancer survivors. The loss of independence among older survivors results in rapidly escalating health care costs (Arozullah et al., 2004).

The purpose of this project was to review and describe the characteristics and functional outcomes of people with a primary diagnosis of cancer who receive inpatient physical rehabilitation. There is a need to explore the general use of physical rehabilitation for cancer survivors. A key question is does age affect functional outcomes for this group. Older cancer survivors are at risk for losses in physical function related to aging, cancer, and its treatments and progressive incapacity (Drouin, 2004). This brief report provides a description of the makeup and the functional outcomes of one population of people, by age, who accessed inpatient rehabilitation for a cancer diagnosis.

Method

This is a retrospective review. Retrospective reviews are useful to build a foundation for future prospective research. This methodology can help focus future study questions, clarify hypothesis, and identify feasibility issues for a prospective study (Hess, 2004).

Sample

The charts of adult patients (18 and above), admitted to an inpatient physical rehabilitation hospital within a 5-year period (January 2004 to December 2008) with a primary diagnosis of cancer, were reviewed. Records were excluded (n = 45) from further analysis if the patient had cancer as a secondary diagnosis and/ or if the patient received rehabilitation services other than inpatient rehabilitation (i.e., home health, outpatient). The charts of 215 patients met inclusion criteria and were used in our analysis. Of the 215, 94 (44%) were 65 and older, 121 (56%) were 64 and younger.

Measures

Demographic variables (age, gender), and common comorbidities (COPD, hypertension, diabetes) were recorded for each patient. Length of stay (LOS) and functional status were also collected during the chart review. Functional status was measured at admission and discharge using the Functional Independence Measure (FIM).

The FIM instrument assesses physical and cognitive disability in terms of burden of care. It has been used to monitor patient progress and to assess outcomes of rehabilitation. It is a rating scale applicable to patients of all ages and diagnoses, by clinicians or by nonclinicians, and has been widely adopted by rehabilitation facilities in the United States and Europe. FIM includes items related to self-care (eating, grooming, upper and lower body dressing, and toileting), mobility (bed, chair or wheelchair, toilet, and tub or shower transfers), locomotion (wheelchair skills or ambulation and stair climbing), sphincter control (bowel and bladder management), communication (comprehension and expression), and social cognition (social interaction, problem solving, and memory; Hamilton, Granger, Sherwin, Zielezny, & Tashman, 1987). The FIM is scored on a 7-point scale, from 1 (dependent) to 7 (independent) with a total score ranging from 18 (totally dependent) to 126 (totally independent).

Interrater tests conducted on patients from 25 facilities by physicians, nurses, and therapists produced intraclass correlation (the 4-point rating version) of .86 for 303 pairs of clinical assessments at admission and .88 for 184 pairs at discharge. Kappa indices of agreement for the 18 items averaged .54. The 7-point rating version, intraclass correlations for pairs of clinicians rating 263 patients ranged from .93 (locomotion subscale) to .96 (self-care and mobility). The mean kappa index of agreement between ratings for each items was .71. Alpha coefficients of .93 (admission) and .95 (discharge) were also found in 11,102 rehabilitation patients. The internal consistency of the locomotion subscale was lower, .68 (Granger, 1982; Granger, & McNamara, 1982).

Content validity has been assessed. A Rasch analysis supported the division into motor and cognitive components; contrasting patterns of responses of different patient groups reflected the types of disability to be expected. Granger examined the predictive validity of the FIM™ in multiple sclerosis patients over a 7-day period. The FIM™ items predicted the time required to provide help for personal care tasks (R2 = .77); correlations for several items exceeded .80; a change of one point on the FIM™ total score represented 3.8 min of care per day. Similar analyses for stroke patients (N = 21) yielded an R2 of .65. Of 11,102 patients, Dodds, Martin, Stolov, and Deyo (1993), found that FIM™ scores improved between admission and discharge and reflected the patients’ destinations. Scores also reflected the presence of coexisting conditions and the severity of impairments.

Burden of care can be approximated using the FIM instrument. An average FIM instrument item rating of 3 or a total-FIM instrument rating of 60 is equivalent to the patient’s needing help from another person for approximately 4 hr per day, each and every day of the year, just to perform basic personal care activities. Generally, a total-FIM instrument rating of 80 to 90 is equivalent to a need for 1 to 2 hr of help each day from another person to perform personal care activities (Granger, Deutsch, Russell, Black, & Ottenbacher, 2007).

The FIM Efficiency Index is a standard outcome measure that has been reported by the Uniform Data System for Medical Rehabilitation (UDSMR) since the 1980s. It is widely reported by researchers in medical rehabilitation (Granger & Hamilton, 1990). FIM efficiency scores are calculated by dividing the total improvement in FIM score by LOS. FIM efficiency is an important calculation that describes compares outcomes with the length of time in therapy that change took (Greenberg, Treger, & Ring, 2006).

Appropriate patients were identified through the hospital database using International Classification of Disease, Ninth Revision (ICD-9) codes. All patients received a comprehensive rehabilitation program, including medical and nursing management and 3 hours a day of physical, occupational, and/or speech therapies. This study was approved by the hospital’s institutional review board.

Statistical Analysis

Data were analyzed using SPSS version 18 for Windows. Descriptive statistics were calculated and univariate statistical analyses were used to determine relationships among variables. Differences in group means were calculated using t tests to determine if there were significant differences (α ≤ .05) between group means for continuous variables. Significant differences in categorical variables were calculated using Pearson chi-square statistics. Functional gains were analyzed using paired t tests to determine if there was a significant improvement in FIM scores from admission to discharge.

Findings

Patient characteristics

Two hundred fifteen patients were discharged after receiving inpatient physical rehabilitation for functional loss resulting from cancer or its treatment from 2004 through 2008.

Characteristics and outcomes of all participants

Table 1 illustrates the data related to the total cancer rehabilitation participant population. The mean age was 61.5 years (SD = 15.8) with a range from 18 to 90 years. Gender was evenly distributed with 109 (51%) females and 106 (49%) male. The mean LOS was 16 days (SD = 1.5) with a range of 2 to 24 days. The most common comorbidities were diabetes (23%), COPD (16%) and hypertension (60%). Often there were multiple comorbidities, with 22% having no comorbidities, 40% having one, 28% with two, and 9% with all three. Significant functional motor gains (p < .0001) were made from admission (mean motor FIM = 34) to discharge (mean motor FIM = 54) as well as cognitively (admission cognitive FIM = 25, discharge FIM = 28, p < .0001). Regardless of age, patients achieved significant functional improvement, as shown by their total FIM scores (t = 23.06, p <.0001), from admission (FIM = 61) to discharge (FIM = 85). Finally the mean LOS efficiency score, average gain in FIM score per day, was 1.9 (SD = 1.5) with a range from –2.6 to 7.4.

Table 1.

Characteristics of All Cancer Participants (N=215)

Admission Discharge P- value
Age 61.5±15.8
Gender
Male 106 (49%)
Female 109 (51%)
MeanLength of Stay 16±9 (2–64)
Mean LOS Efficiency 1.9±1.5 (−2.6–7.4)
Comorbidities
Diabetes 50 (23%)
COPD 34 (16%)
Hypertension 129 (60%)
Multiple Comorbidities
0 47 (22%)
1 85 (40%)
2 61 (28%)
3 19 (9%)
Mean Total FIM Score 61±17 (18–115) 85±22.5(18–122) <.0001
Mean FIM Motor Score 34±12.6(11–75) 54±17(12–81) <.0001
Mean FIM Cognitive Score 25±7.5(5–40) 28±9(5–97) <.0001

NOTE: Note: LOS = length of stay, COPD = Chronic Obstructive Pulmonary Disease, and FIM = functional independence measure. Values are M ± SD (range).

Characteristics and outcomes by age groups

Data from the chart reviews were also analyzed by age group. The findings are presented in Table 2. Stratifying by age, 121 (56%) were 64 and younger, 94 (44%) were 65 and older.

Table 2.

Characteristics of Cancer Rehabilitation Patients Compared by Age

<65 years (N=121) ≥65 years (N=94) P-value
Gender 0.292
Male 64(52.9%) 42(44.7%)
Female 57 (47.1%) 52 (55.3%)
Mean Length of stay 17±10 (2–64) 15±7.9 (2–37) 0.171
LOS Efficiency 1.8±1.5 (−2.6–7.4) 1.9±1.6 (−2.57–6.6) 0.517
Comorbidities
Diabetes 24(19.8%) 26(27.7%) 0.204
COPD 15(12.4%) 19(20.2%) 0.134
Hypertension 62(51.2%) 66(70.2%) 0.005
Multiple Comorbidities
0 34(28.1%) 17(18.1%) 0.025
1 48(39.7%) 45(47.9%) 0.875
2 29(24%) 30(31.9%) 0.124
3 10(8.3%) 2(2.1%) 0.770
Mean Total FIM Admission Score 61±18(18–101) 60±17(27–115) 0.632
Mean Total FIM Discharge Score 85±23(18–116) 85±22(27–122) 0.904
Total FIM Change Score 24±16.5(−27–60) 25±14(−18–60) 0.329
Mean FIM Admission Motor Score 35.2±12.7 (11–62) 34.7±12.5 (12–75) 0.723
Mean FIM Discharge Motor Score 53.8±17.5 (12–81) 55.1±17.2 (12–81) 0.690
Mean FIM Admission Cognitive Score 25.1±8.0 (5–40) 24.5±7.0 (8–40) 0.574
Mean FIM Discharge Cognitive Score 28.3±8.5 (5–67) 27.9±9.6 (8–97) 0.662

Note: LOS = length of stay. Values are M ± SD (range).

There were very few significant differences between the age groups (<65 and ≥65). The only significant differences emerged in the area of comorbidities. As shown in Table 2, there was a significant difference in the number of patients with hypertension by age group (51%, <65, and 70%, ≥5.057, p = .025). The younger group had a significantly higher chance of having no comorbidities as compared with the older group. There was no significant difference between the age groups in terms of those who did have comorbidities by type or number. In addition, there was no significant difference in the FIM admission or discharge scores by age group (Table 2). There were no significant differences in LOS or LOS efficiency. Table 2 shows that both age groups made significant gains in motor, cognitive, and total FIM scores after treatment.

Descriptively, Table 3 shows the outcomes according to the FIM score by functional level. Broken down by age category and as a total of all cancer patients, there were significant gains in functional level in all three categories. The <65 years group had a 33.9% decrease in maximum assistance category, a 13.2% decrease in the moderate assistance category and a 47% increase in minimal to no assistance category (p < .0001). The ≥65 group had a 28.7% decrease in maximum assistance category, a 14.9% decrease in the moderate assistance category, and a 43.6% increase in minimal to no assistance category (p < .0001). In total, all the cancer rehabilitation participants had a 32% decrease in maximum assistance category, a 14% decrease in the moderate assistance category, and a 46% increase in minimal to no assistance category (p < .0001).

Table 3.

FIM Functional Category Outcomes by Age

Total FIM Functional
Score Admission
Total FIM Functional
Score Discharge
% Change P-Value
<65 (N=121) <0.0001
0–60 Max Assist 58(47.9%) 17(14%) ↓33.9%
61–90 Mod Assist 58(47.9%) 42(34.7%) ↓13.2%
91–126 Min to No Assist 5(4.1%) 62(51.2%) ↑47%
≥65(N=94) <0.0001
0–60 Max Assist 41 (43.6%) 14(14.9%) ↓28.7%
61–90 Mod Assist 49 (52.1%) 35(37.2%) ↓14.9%
91–126 Min to No Assist 4 (4.3%) 45(47.9%) ↑43.6%
Total (N=215) <0.0001
0–60 Max Assist 99 (46%) 30 (14%) ↓32%
61–90 Mod Assist 107 (50%) 78(36%) ↓14%
91–126 Min to No Assist 9 (4%) 107(50%) ↑46%

Discussion

Cancer in an inpatient rehabilitation setting is not generally a primary diagnosis in terms of treatment, and little has been written on functional improvement after rehabilitation for cancer patients (Guo, Shin, Hainley, Bruera, & Palmer, 2011; Marciniak, Sliwa, Spill, Heinemann, & Semik, 1996). As of this time, there are no known care pathways for cancer survivors or cancer rehabilitation, although this was a priority set forth by the Institute of Medicine (Hewitt, Greenfield, & Stovall, 2006). This project allows for the description of one population of cancer survivors who received inpatient rehabilitation. Similar to other research findings these patients displayed multiple comorbidities frequently seen in the rehabilitation setting (Lehmann et al., 1978). However, also similar to other studies, this population showed functional gain after receiving inpatient rehabilitation (Deitz, 1969; Phillip, Ayyangar, Vanderbilt, & Gaebler-Spira, 1994).

Previous studies have shown that 40% to 50% of cancer patients who receive rehabilitation do so because of deconditioning, asthenia, or general weakness (Cole, Scialla, & Bednarz, 2000; Tang, Harvey, Park Dorsay, Jiang, & Rathborn, 2007). Brennan and Warfel (1993) evaluated 50 cancer patients referred to rehabilitation, and on average the patients had 1.7 functional impairments. These included deconditioning (56%), central nervous system dysfunction (36%), and peripheral neurological problems (28%).

Although the chart documentation was too variable in this study to quantitatively demonstrate it, it appears that a number of the patients in this project did indeed come to inpatient rehabilitation related to deconditioning and general weakness. Motor dysfunction seemed to be more prevalent, although cognitive issues would emerge in brain cancer cases as well as potentially related to age; again, we cannot say this conclusively. Motor FIM improvement can be linked to improved quality of life and decreased care burden (Granger, Divan, & Fiedler, 1995). Past studies have evaluated patients with neoplastic brain injuries or spinal cord compressions, who reportedly achieved functional gains comparable with those of patients who did not have cancer (Marciniak, Sliwa, Heinemann, & Semik, 2001; McKinley, Huang, & Tewksbury, 2000; Tang et al., 2007). While the outcomes are crucial, there needs to be more focus on potential differences in the actual therapeutic interventions when comparing a cancer rehabilitation patient with non-cancer rehabilitation patient. This is an area for in-depth future research.

A one-point decrease in total FIM score is equivalent to about 4.1 fewer minutes of caregiver help for people with stroke for people with stroke (Granger et al., 1995). The 24-point improvement of the participant group as a whole in this study translates into approximately 98 min of caregiver time saved per day. When looking at the functional categories (0–60 maximum assistance, 61–90 moderate assistance, and 91–126 minimal to no assistance), the potential for even greater cost savings is illustrated. Granger et al. (2007) state that a score of 60 requires a minimum of 4 hr per day help to perform basic personal care activities. A score of 90 drops that to 1 to 2 hr and more than 91 may result in no personal care help being required. If a person’s functional ability increases from the maximum assistance category to the moderate assistance category, there is the potential for savings of approximately US $17,472 a year if the hourly care is valued at US $12 an hour. This is a significant burden of either time or money for care giving. The inpatient rehabilitation clearly helped move the patients up the scale of independence.

The FIM efficiency number is a useful tool for comparing rehabilitation outcomes. In past studies, the FIM efficiency score has been reported as 1.5 for people with brain tumors (Greenberg et al., 2006), 1.8 in younger patients with traumatic brain injury (Granger et al., 2010), and 1.6 in older patients who have had a stroke (Granger et al., 2009). Our group of cancer patients had a LOS efficiency number of 1.9, not far off from the other diagnoses.

The LOS, which leads to the analysis of cost of stay and rehabilitation efficiency, was not significantly different between these groups either. Perhaps the most startling similarity of the two age groups was the incidence of comorbidity and the number of comorbidities the patient presented with. The assumption might have been that the older group would potentially be sicker, with more comorbodities which would in turn result in longer lengths of stay and poorer functional outcomes. None of those assumptions held true in the population reviewed in this project. In fact, it can be hypothesized that, in this situation, the people who are referred to inpatient cancer rehabilitation are less healthy younger people and healthier older people. This would be one of many questions surrounding this topic that could be better understood through future research.

While cancer rehabilitation is underused by all, there is a risk that older cancer survivors may receive less rehabilitation due to the mistaken belief that they have less of a chance for functional improvement. This project shows that there was little difference as a whole and no functional difference between those younger than 65 years old and those 65 years old and above. Both age groups improved with rehabilitation care pointing toward the importance of rehabilitation services for cancer survivors regardless of age.

Our study was limited in several ways. First, it was a retrospective study and therefore patients were preselected for admission because they were regarded as likely to benefit from rehabilitation. As a retrospective chart review, the sample is a convenience one. Second, the types of cancer represented in this study do not reflect the distribution of cancer types in the United States. Referral patterns certainly influenced these findings. Finally, there is no follow-up in terms of more long-term functional outcomes, quality of life, and satisfaction with inpatient rehabilitation for patients with a primary diagnosis of cancer. The goal of this project is to bring awareness to cancer rehabilitation and to raise questions for future research.

As this is a retrospective chart review, no conclusions can be made, but questions for future research can be raised. A major consideration is how inpatient rehabilitation treatment affected overall quality of life for these patients, which is a question that cannot be answered from these data but may interact with the need and effect of rehabilitation services regardless of future length of life.

Future research into the quality-of-life impact of inpatient rehabilitation for cancer diagnoses needs to be considered to determine this relationship. A second question that emerges is “who does not receive cancer rehabilitation and why.” A cost-to-benefit ratio also needs to be further evaluated to determine how such services contributed to the survival and quality of life of these patients. In terms of evidence-based practice, much of cancer rehabilitation is in its infancy; without doubt, age is a variable that needs to be further explored and better understood.

Conclusion

In this retrospective chart review, people who receive inpatient rehabilitation for a primary diagnosis of cancer made significant functional improvements. This held true regardless of age. The results of this study have important implications for health care practitioners working with aging cancer survivors. Physical rehabilitation should be on the menu of treatment for appropriate cancer survivors. The connection between oncology and rehabilitation needs to be strengthened. As that partnership is developed, it is important to know that age may not be a factor in whether a cancer survivor is a good candidate for rehabilitation.

Acknowledgments

Funding

The authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This project was funded by the National Cancer Institute (R03-CA136444-01).

Biographies

Elizabeth G. Hunter, PhD, is the Director of Research at Cardinal Hill Rehabilitation Hospital in Lexington, Kentucky. Her research interests include clear health communication, rural health and cancer.

Julie Baltisberger, MS, OTR/L 2, is a faculty member in the Eastern Kentucky University Occupational Therapy department. Her research interest is related to functional performance and cancer survivorship.

Footnotes

Declaration of Conflicting Interests

The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

References

  1. Arozullah AM, Calhoun EA, Wolf M, Finley DK, Fitzner KA, Heckinger EA, Gorby NS, Schumock GT, Bennett CL. The financial burden of cancer: Estimates from a study of insured women with breast cancer. Journal of Supportive Oncology. 2004;2:271–278. [PubMed] [Google Scholar]
  2. Bond SM. Crossing the threshold of cancer and aging. Journal of Gerontological Nursing. 2010;36(2):3–4. doi: 10.3928/00989134-20100108-04. [DOI] [PubMed] [Google Scholar]
  3. Brennan MJ, Warfel BS. Musculoskeletal complications of cancer: A survey of 50 patients. Journal of Back and Musculoskeletal Rehabilitation. 1993;3:1–6. doi: 10.3233/BMR-1993-3204. [DOI] [PubMed] [Google Scholar]
  4. Center for Disease Control and Prevention. The state of aging and health in America, 2002–2007. 2007 Retrieved from http:/www.cdc.gov/aging.
  5. Cheville AL, Troxel AB, Basford JR, Kornblith AB. Prevalence and treatment patterns of physical impairments in patients with metastatic breast cancer. Journal of Clinical Oncology. 2008;26:2621–2629. doi: 10.1200/JCO.2007.12.3075. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Cole RP, Scialla SJ, Bednarz L. Functional recovery in cancer rehabilitation. Archives of Physical Medicine & Rehabilitation. 2000;81:623–627. doi: 10.1016/s0003-9993(00)90046-7. [DOI] [PubMed] [Google Scholar]
  7. Deitz JH. Rehabilitation of the cancer patient. Medical Clinics of North America. 1969;53:607–624. [PubMed] [Google Scholar]
  8. Demark-Wahnefried W, Morey MC, Sloane R, Snyder DC, Cohen HJ. Promoting health lifestyles in older cancer survivors to improve health and preserve function. Journal of the American Geriatrics Society. 2009;57:S262–S264. doi: 10.1111/j.1532-5415.2009.02507.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Dodds TA, Martin DP, Stolov WC, Deyo RA. A validation of the Functional Independence Measurement and its performance among rehabilitation inpatients. Archives of Physical Medicine & Rehabilitation. 1993;74:531–536. doi: 10.1016/0003-9993(93)90119-u. [DOI] [PubMed] [Google Scholar]
  10. Drouin J. Exercise in older individuals with cancer. Topics in Geriatric Rehabilitation. 2004;20(2):81–97. [Google Scholar]
  11. Ershler WB. Biological Interactions of Aging and Anemia: A focus on Cytokines. Journal of the American Geriatrics Society. 2003;51:18–21. doi: 10.1046/j.1532-5415.51.3s.2.x. [DOI] [PubMed] [Google Scholar]
  12. Feuerstein M. Cancer survivors need evidence on how to optimize physical function. Journal of Cancer Survivorship. 2009;3:73–74. doi: 10.1007/s11764-009-0090-5. [DOI] [PubMed] [Google Scholar]
  13. Fialka-Moser V, Crevenna R, Korpan M, Quittan M. Cancer rehabilitation: Particularly with aspects of physical impairments. Journal of Rehabilitation Medicine. 2003;35:153–162. doi: 10.1080/16501970306129. [DOI] [PubMed] [Google Scholar]
  14. Ganz PA, Guadagnoli E, Landrum MB, Lash TL, Rakowski W, Silliman RA. Breast cancer in older women: Quality of life and psychosocial adjustment in the 15 months after diagnosis. Journal of Clinical Oncology. 2003;21:4027–4033. doi: 10.1200/JCO.2003.08.097. [DOI] [PubMed] [Google Scholar]
  15. Guo Y, Shin KY, Hainley S, Bruera E, Palmer JL. Inpatient rehabilitation improved functional status in asthenic patients with solid and hematologic malignancies. American Journal of Physical Medicine & Rehabilitation. 2011;90:265–271. doi: 10.1097/PHM.0b013e3182063ba6. [DOI] [PubMed] [Google Scholar]
  16. Granger CV. Health accounting-functional assessment of the long-term patient. In: Kottke FJ, Stillwell GK, Lehmann JF, editors. Krusen’s handbook of physical medicine and rehabilitation. 3rd ed. Philadelphia, PA: W.B. Saunders; 1982. pp. 253–274. [Google Scholar]
  17. Granger CV, Deutsch A, Russell C, Black T, Ottenbacher KJ. Modifications of the FIM instrument under the inpatient rehabilitation facility prospective payment system. American Journal of Physical Medicine & Rehabilitation. 2007;86:883–892. doi: 10.1097/PHM.0b013e318152058a. [DOI] [PubMed] [Google Scholar]
  18. Granger CV, Divan N, Fiedler RC. Functional assessment scales: A study of persons after traumatic brain injury. American Journal of Physical Medicine & Rehabilitation. 1995;74:107–113. [PubMed] [Google Scholar]
  19. Granger CV, Hamilton BB. UDS Report: The Uniform Data System for Medical Rehabilitation report for first admissions for 1990. American Journal of Physical Medicine & Rehabilitation. 1990;71:108–113. [PubMed] [Google Scholar]
  20. Granger CV, Markello SJ, Graham JE, Deutsch A, Reistetter TA, Ottenbacker KJ. The uniform data system for medical rehabilitation: Report of patients with stroke discharged from a comprehensive medical program in 2000–2007. American Journal of Physical Medicine & Rehabilitation. 2009;88:961–972. doi: 10.1097/PHM.0b013e3181c1ec38. [DOI] [PubMed] [Google Scholar]
  21. Granger CV, Markello SJ, Graham JE, Deutsch A, Reistetter TA, Ottenbacker KJ. The uniform data system for medical rehabilitation: Report of patients with traumatic brain injury discharged from rehabilitation programs in 2000–2007. American Journal of Physical Medicine & Rehabilitation. 2010;89:265–278. doi: 10.1097/PHM.0b013e3181d3eb20. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Granger CV, McNamara MA. Functional assessment utilization: The Long-Range Evaluation System (LRES) In: Granger CV, Gresham GE, editors. Functional assessment in rehabilitation medicine. Baltimore, MD: Williams and Wilkins; 1982. pp. 99–121. [Google Scholar]
  23. Greenberg E, Treger I, Ring H. Rehabilitation outcomes in patients with brain tumors and acute stroke: Comparative study of inpatient rehabilitation. American Journal of Physical Medicine Rehabilitation. 2006;85:568–573. doi: 10.1097/01.phm.0000223218.38152.53. [DOI] [PubMed] [Google Scholar]
  24. Hamilton BB, Granger CV, Sherwin FF, Zielezny M, Tashman JS. A uniform national data system for medical rehabilitation. In: Fuhrer MH, editor. Rehabilitation outcomes: Analysis and measurement. Baltimore, MD: Paul H Brooks; 1987. pp. 137–147. [Google Scholar]
  25. Hess DR. Retrospective studies and chart reviews. Respiratory Care. 2004;49:1171–1174. [PubMed] [Google Scholar]
  26. Hewitt M, Greenfield S, Stovall E. From cancer patient to cancer survivor: Lost in transition. Washington, DC: National Academies Press; 2006. [Google Scholar]
  27. Kroenke CH, Rosner B, Chen WY, Kawachi I, Colditz GA, Holmes MD. Functional impact of breast cancer by age at diagnosis. Journal of Clinical Epidemiology. 2004;22:1849–1856. doi: 10.1200/JCO.2004.04.173. [DOI] [PubMed] [Google Scholar]
  28. Lehmann JF, Delisa JA, Warren CG, deLateur BJ, Bryant PLS, Nicholson CG. Cancer rehabilitation: Assessment of need, development, and evaluation of model of care. Archives of Physical Medicine & Rehabilitation. 1978;59:410–419. [PubMed] [Google Scholar]
  29. Marciniak CM, Sliwa JA, Heinemann AW, Semik PE. Functional outcomes of persons with brain tumors after inpatient rehabilitation. Archives of Physical Rehabilitation Medicine. 2001;82:457–463. doi: 10.1053/apmr.2001.21862. [DOI] [PubMed] [Google Scholar]
  30. Marciniak CM, Sliwa JA, Spill G, Heinemann AW, Semik PE. Functional outcome following rehabilitation of the cancer patient. Archives of Physical Medicine Rehabilitation. 1996;77:54–57. doi: 10.1016/s0003-9993(96)90220-8. [DOI] [PubMed] [Google Scholar]
  31. McKinley WO, Huang ME, Tewksbury MA. Neoplastic vs. traumatic spinal cord injury: An inpatient rehabilitation comparison. American Journal of Physical Medicine & Rehabilitation. 2000;79:138–144. doi: 10.1097/00002060-200003000-00005. [DOI] [PubMed] [Google Scholar]
  32. Movsas SB, Chang VT, Tunkel RS, Shah VV, Ryan LS, Millis SR. Rehabilitation needs of an inpatient medical oncology unit. Archives of Physical Medicine and Rehabilitation. 2003;84:1642–1646. doi: 10.1053/s0003-9993(03)00345-9. [DOI] [PubMed] [Google Scholar]
  33. Nomori H, Watanabe K, Ohtsuka T, Naruke T, Suemasu K. Six-minute walking and pulmonary function test outcomes during the early period after lung cancer surgery with special reference to patients with chronic obstructive pulmonary disease. Japanese Journal of Thoracic and Cardiovascular Surgery. 2004;52:113–119. doi: 10.1007/s11748-004-0126-8. [DOI] [PubMed] [Google Scholar]
  34. Phillip PA, Ayyangar R, Vanderbilt J, Gaebler-Spira DJ. Rehabilitation outcome in children after treatment of primary brain tumor. Archives of Physical Medicine and Rehabilitation. 1994;75:36–38. [PubMed] [Google Scholar]
  35. Ries L, Melbert D, Krapcho M, Mariotto A, Miller BA, Feuer EJ, Edwards BK. SEER Cancer Statistical Review, 1975–2004. Bethesda, MD: National Cancer Institute; 2007. [Google Scholar]
  36. Schrag D, Cramer LD, Bach PB, Begg CB. Age and adjuvant chemotherapy use after surgery for stage III colon cancer. Journal of the National Cancer Institute. 2001;93:850–857. doi: 10.1093/jnci/93.11.850. [DOI] [PubMed] [Google Scholar]
  37. Smith BD, Smith GL, Hurria A, Hortobagyi GN, Buchholz TA. Future of cancer incidence in the United States: Burdens upon an aging, changing nation. Journal of Clinical Oncology. 2009;27:2758–2765. doi: 10.1200/JCO.2008.20.8983. [DOI] [PubMed] [Google Scholar]
  38. Tang V, Harvey D, Park Dorsay J, Jiang S, Rathborn MP. Prognostic indicators in metastatic spinal cord compression: Using Functional Independence Measure and Tokuhashi scale to optimize rehabilitation planning. Spinal Cord. 2007;45:671–677. doi: 10.1038/sj.sc.3102024. [DOI] [PubMed] [Google Scholar]
  39. Vargo MM. The oncology–rehabilitation interface: Better systems needed. Journal of Clinical Oncology. 2008;26:2610–2611. doi: 10.1200/JCO.2008.16.6850. [DOI] [PubMed] [Google Scholar]
  40. Warfel BS, Lachmann E, Nagler W. Physiatric evaluation of the cancer patient. Journal of Back and Musculoskeletal Rehabilitation. 1993;3:60–68. doi: 10.3233/BMR-1993-3210. [DOI] [PubMed] [Google Scholar]

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