Skip to main content
NIHPA Author Manuscripts logoLink to NIHPA Author Manuscripts
. Author manuscript; available in PMC: 2012 Nov 1.
Published in final edited form as: Arch Phys Med Rehabil. 2011 Nov;92(11):1770–1775. doi: 10.1016/j.apmr.2011.05.024

Health, Secondary Conditions, and Life Expectancy after Spinal Cord Injury

James S Krause 1, Lee L Saunders 1
PMCID: PMC3385509  NIHMSID: NIHMS384135  PMID: 22032212

Abstract

Objective

To evaluate the association of health status, secondary health conditions, hospitalizations, and risk of mortality and life expectancy (LE) after spinal cord injury (SCI).

Design

Prospective cohort study.

Setting

Preliminary data were collected from a specialty hospital in the Southeastern United States, with mortality follow-up and data analysis conducted at a medical university.

Participants

A total of 1361 adults with traumatic SCI, all at least 1 year post-injury at the time of assessment, were enrolled in the study. There were 325 deaths. After elimination of those with missing data on key variables, there were 267 deaths and 12,032 person-years.

Interventions

None

Main Outcome Measures

Mortality status was determined by routine follow-up using the National Death Index through December 31, 2008. A logistic regression model was developed to estimate the probability of dying in any given year using person years.

Results

A history of chronic pressure ulcers, amputations, a depressive disorder, symptoms of infections, and being hospitalized within the past year were all predictive of mortality. LE estimates were generated using the example of a male with non-cervical, non-ambulatory SCI. Using 3 age examples (20, 40, 60), the greatest estimated lost LE was associated with chronic pressure ulcers (50.3%), followed by amputations (35.4%), 1 or more recent hospitalizations (18.5%), and the diagnosis of probable major depression (18%). Symptoms of infections was associated with a 6.7% reduction in LE for a 1 standard deviation increase in infectious symptoms.

Conclusion

Several secondary health conditions represent risk factors for mortality and diminish LE after SCI. The presence of 1 or more of these factors should be taken as an indicator of the need for intervention.

Keywords: spinal cord injury, mortality, risk, health, economics, life expectancy


Research over the past 3 decades has documented diminished LE after the onset of SCI, with LE inversely proportional to injury severity.13 Although LE has decreased during the first year post-injury, it appears stable after the first year post-injury.24 Since medical management is no longer improving long-term survival rates, epidemiologic studies are needed to identify risk factors for premature mortality, allowing professionals to apply proven intervention strategies to enhance LE. These studies will be most successful when they systematically address multiple risk factors, allowing for diverse intervention strategies.

Krause5 developed a theoretical risk model [1996] to guide investigations of prediction of LE by accounting for multiple sets of predictive factors including biographic and injury, psychological, socio-environmental, behavioral, and health variables. According to the model, health factors are the most immediate and most important predictors of LE. Health factors may be specific secondary conditions, such as pressure ulcers, or more general indicators of a history of treatment (e.g., hospitalization).6 They mediate the relationships between health behaviors,7 such as smoking and alcohol misuse, with LE. Psychological factors,8 such as personality characteristics, and socio-environmental factors,9 such as poverty or social support, have less direct impact on LE according to the model. Studies of health factors and mortality after SCI are rare, and findings are not typically translated into differential LE. Studies of causes of death have indicated heart disease, external causes, and respiratory complications as the leading causes of death after the first year post-injury,2,10 but they do not fully account for the health factors that may lead to diminished LE. Utilizing data from the NSCISC, a network of facilities in the USA contributing data to a common database, several health factors were identified as risk factors including self-rated health, hospitalizations, and having a grade 3 or 4 PU.4 Another study found having heart disease was predictive of mortality.11 Although other chronic diseases, including diabetes, hypertension, chronic obstructive pulmonary disease, and asthma were not significant predictors of mortality, the sample was small (n=361, 37 deaths). These studies are limited to mostly basic demographic and injury characteristics that do not help clarify the role of diverse sets of variables in relation to mortality and LE.

In the first of 2 analyses of data from prospective cohort studies, 5 health factors were significantly related to mortality after controlling for demographic and injury characteristics among a sample of 1265 participants over a 7- to 8-year interval (188 deaths).6 These included days spent in the hospital, amputations or fractures, infections, surgeries for PUs, and PMD. In the second analysis systematically evaluating all components of the full theoretical risk model, 4 health predictors were retained in the model (all except infectious symptoms), along with 2 behavioral factors (prescription medication use, binge drinking days) and 1 environmental factor (low income).12

Only a handful of studies examined LE directly, nearly all of which have used NSCISC data. DeVivo et al.2 reported LE for various ages and injury levels and found the percentage of LE lost ranged from 11.8% for a 20 year old male with a Frankel D injury to 69.5% for a same aged male who was also ventilator dependent. Krause, DeVivo, and Jackson4 subsequently evaluated a broader range of predictors of mortality and LE. Under favorable health assumptions alone, LE was 56.4% for a person age 50 and 64.8% for a person age 25. Although health factors were considered, 2 socioeconomic factors, workers compensation insurance and the economic subscale from the CHART, were the primary factors associated with greater longevity. Strauss et al.13 replicated this analysis after the accrual of time and more deaths, finding less substantial effects of economic factors on LE (workers compensation was no longer significant). However, when using actual family income, rather than the CHART subscale, Krause Saunders, and DeVivo14 found much more substantial effects of economic factors on LE. Two additional studies utilized non-NSCISC data, demonstrating again the importance of familial income15 and risk behaviors with LE.16 For instance, after controlling for demographic and injury characteristics, smoking, binge drinking, use of prescription medication, and less days out of the house were significantly associated with decreases in LE.16

Summary and Purpose

The existing literature, both conceptual and empirical, clearly implicates secondary health conditions as elevating risk of mortality. By definition, these factors would also lead to diminished LE, although these relationships have never been quantified. However, LE has infrequently been reported in the literature and, with 2 exceptions, has been restricted to analysis of NSCISC data. Our purpose was to evaluate the relationship of secondary health conditions and hospitalizations with LE after SCI. All analyses follow the theoretical risk model, which has been the focus of recent research.5 The first set of risk factors within the theoretical risk model (demographic and injury characteristics including age, sex, injury severity) are used as statistical controls, with the primary focus on health factors which are the most important predictors within the risk model. Therefore, health factors are evaluated after controlling for demographic and injury characteristics.

Methods

Participants

After receiving Institutional Review Board approval, participants were identified from records of a specialty hospital in the Southeastern United States. There were 3 inclusion criteria: (1) traumatic SCI with some residual impairment, (2) 18 years or older, and (3) minimum of 12 months post-injury. Of 1929 potential participants, 1386 (72%) completed an assessment related to health and secondary conditions. We excluded 25 participants with questionable diagnoses or no date of injury or age, leaving 1,361 for analysis. Figure 1 summarizes participant inclusion in the final analysis.

Figure 1.

Figure 1

Flowchart of participant inclusion in the final analysis.

Procedures

Cover letters were sent to 1929 potential participants to describe the study and explain informed consent. Materials were sent 4 to 6 weeks later. Non-respondents received 2 follow-up mailings and a follow-up phone call. Additional materials were sent if requested by the participant. Participants (n=1386, 72% response rate) received $20 remuneration, and drawings were conducted totaling $1500. Prospective data were collected between July 1997 and April 1998. Mortality status was assessed as of December 31, 2008, the most recent available data using the NDI.17 Participants who were not found deceased were presumed to be alive as of that date.

Variables and Measures

Demographic and injury variables were included as statistical controls, including sex, age at injury, years since injury, and injury severity. Injury severity was classified into 4 categories using a scheme identical to that used in preliminary studies69,12 and similar to the NSCISC.4 All non-ambulatory participants were classified according to 3 neurologic levels (C1–C4, C5–C8, non-cervical), whereas ambulatory participants were grouped together regardless of neurologic level (ambulatory status is a proxy for ASIA D).

We measured 5 indicators of health and secondary conditions, including: (a) PU history, (b) PMD (yes/no), (c) symptoms of infections, (d) amputations, and (e) hospitalization. The OAHMQ was used to measure PMD.18 It is a 22-item measure which was standardized such that scores above the cutoff of 11 indicate PMD. The OAHMQ has been used in previous studies to assess PMD among community dwelling participants with SCI.19 Kemp and Adams31 reported a test-retest coefficient of .87 (p < .001) and alphas were .93 (p < .001). In terms of validity, sensitivity and specificity were reported to be .93 and .87, respectively. A recent study comparing the OAHMQ to the abbreviated version of the Patient Health Questionnaire indicated the OAHMQ produces modestly higher rates of depression.20

Symptoms of infection included fevers, sweats and chills, and urinary tract infections in the 12 months prior to the study. Participants were asked the number of occurrences (0, 1–2, 3–6, 7–12, ≥13). A summary measure (summated score) was created similar to that previously reported in the literature.6 Amputations were defined by having 1 or more upper or lower extremity amputations since SCI onset. Hospitalizations within the last year were dichotomized. PUs was defined as “open sores in pressure areas, such as your tailbone, ischium, heel, elbows.” PU history was self-classified as: 1) never had PU, 2) only immediately after injury, but rarely since, 3) every couple of years, 4) at least 1 PU per year, and 5) always seem to have PU. For data analysis, we collapsed the middle 3 responses leaving: 1) no history of PU; 2) non-chronic PU (categories 2, 3, 4); and 3) chronic PU.

Statistical Considerations

We used a 2 stage hierarchical model building strategy with a logistic regression model and mortality as our outcome. Person-year data was constructed using the time from survey to mortality or to censoring (December 31, 2008). This method treats each follow-up year for each person as a separate observation.21 These methods have been used in previous mortality analyses,4,22 and logistic regression was conducted on the person-year dataset, with mortality as the outcome. This method allows the researcher to take into account varying covariates across time in the calculation of life expectancy.

The first analysis included only demographic and injury characteristics as a baseline model. In stage 2, health variables were added. PU history (reference=none), PMD (reference=no), hospitalizations (reference=0), and amputation (reference=no) were entered as categorical variables and infectious symptoms as a continuous variable. Symptoms of infection was standardized, and the odds of mortality for 1 standard deviation were reported. Hosmer-Lemeshow and global χ2 tests were used to assess goodness-of-fit of the model.23 The C-statistic, measuring area under the Receiver Operating Characteristic curve, was used to assess discriminatory ability.23 A value of 0.5 for the C-statistic represents no better than chance prediction, and C-statistic values approaching 1 represent improved discrimination of the model. ORs with 95% CIs were calculated. We calculated differences in LE by calculating the probability of survival for each year of life through age 100 using methods widely reported in the literature.15,16,21,24 When calculating life expectancy for different health conditions, all other health outcomes were held to their reference level (i.e. when assessing life expectancy for PMD, all other health conditions were kept at their reference level – specified above).

Results

Participant Characteristics

There were 194 participants (14.3%) with missing data on at least 1 variable. Deceased cases were disproportionately represented among those with missing data (17.9% of the deceased had missing data compared with 13.1% of the survivors; p=<.05). Significant differences were also observed for race, as 63.9% of those with missing data were white compared with 76.9% of those with complete data (p<.05). The average age of onset of those with missing data (34.8) was greater than those without missing data (31.3, p<.001).

There were no differences as a function of sex, injury severity, or injury duration. There were 1,167 participants in the final statistical model, of which 267 (22.9%) died. Mean age at injury was 31.1 years (standard deviation=13.5), with an average of 9.6 (standard deviation =6.8) years since injury. 21.5% of participants were ambulatory. The majority were white (76.9%) and male (74.4%).

Modeling

In the base logistic regression model including only demographic and injury characteristics, chronologic age, years since injury, and injury severity were significant (table 1). The second stage added health conditions to the base model. Each of the 5 health factors were significant in stage 2 (table 2), although years since injury was no longer significant. Compared with the reference group (ambulatory), there were greater odds of mortality with each successive increase in injury severity. Additionally, odds of mortality increased with increasing age and years since injury.

Table 1.

Odds ratios, 95% confidence intervals, and mortality rates as a function of demographic and injury characteristics.

Demographic/Injury Characteristics Mortality
OR* (95% CI) p-value
Yes (n=267) No (N=900)

Row %
Gender
 Male (n=868) 23.7 76.3 1.17 (0.88–1.68) 0.3841
 Female (n=299) 20.4 79.6 Reference
Injury Severity
 C1–C4 (n=158) 36.7 63.3 7.33 (4.14–12.95) <.0001
 C5–C8 (n=356) 25.3 74.7 3.77 (2.27–6.26)
 Non-cervical (n=402) 20.9 79.1 2.58 (1.58–4.24)
 Ambulatory (n=251) 13.9 86.1 Reference
Years Since Injury 10.4 (7.3) 9.3 (6.6) 1.07 (1.05–1.10) <.0001
Age at Survey 49.7 (15.3) 38.0 (11.4) 1.08 (1.06–1.10) <.0001
*

OR are controlling for all other variables in the table.

Table 2.

Adjusted odds ratios and 95% confidence intervals for the risk variables from the final model.

Variable Final Model
OR* 95% CI p-value
Gender (vs. Female) 0.1442
Male 1.26 0.96–1.83
Age (vs. 18–34) <.0001
35–39 1.74 0.93–3.26
40–44 2.80 1.57–5.01
45–49 2.47 1.35–4.54
50–54 3.77 2.11–6.73
55–59 4.24 2.32–7.75
60–64 6.48 3.46–12.12
65–69 9.60 4.93–18.69
70–74 19.02 10.05–35.99
75–79 28.80 14.37–57.72
80+ 41.94 19.32–91.04
Injury Severity (vs. Ambulatory) <.0001
 C1–C4 3.06 1.90–4.92
 C5–C8 1.86 1.19–2.91
 Non-cervical 1.53 0.98–2.39
Years Since Injury (vs. 10–19) 0.6299
 1–4 1.68 0.98–2.39
 5–9 0.95 0.65–1.37
 20–29 1.11 0.81–1.51
 30+ 1.01 0.60–1.70
Pressure Ulcers (vs. Never get them) <.0001
Non-chronic 1.46 1.08–1.97
Chronic 4.52 2.57–7.94
Probable Major Depression (vs. No) 0.0009
Yes 1.60 1.21–2.11
Hospitalizations (vs. None) 0.0006
1+ 1.63 1.23–2.14
Amputation (vs. No) 0.0018
Yes 2.69 1.44–5.02
Infections** 1.18 1.03–1.36 0.0159
*

controlling for age, gender, years post-injury, injury severity

**

OR reported is for 1 sd change in infectious symptoms

Of the health factors, those who had chronic PUs had 4.52 greater odds of mortality (CI = 2.57, 7.94) and those with non-chronic PUs had a 1.46 greater odds of mortality (CI = 1.08, 1.97). Amputation was associated with a 2.69 greater odds of mortality (CI = 1.44, 5.02). Having been hospitalized at least once in the year prior to the data collection was associated with a 1.63 greater odds of mortality (CI = 1.23, 2.14). A diagnosis of PMD was associated with a greater odds of mortality (OR = 1.60; CI = 1.21, 2.11). Symptoms of infections was also related to mortality, with an increase of 1 standard deviation of infectious symptoms associated with 1.18 greater odds (CI = 1.03–1.36).

Life Expectancy

LE calculations were made for each health condition (table 3) using the results from the final model (table 2). We used a male, injured at 19, with a non-cervical, non-ambulatory injury as the example. Three different age examples are provided: 20, 40, and 60 years. Under favorable conditions (no health risk factors), LE was 45.6 years at 20, an additional 28.7 years at 40, and 14.2 years at 60. The projected lost LE associated with each condition increased with age. The greatest average decline in LE was associated with chronic PUs (50.3%), with substantially less reduction for non-chronic (14.6%). Of the dichotomous variables, the greatest percentage of lost LE was for amputation (35.4%), followed by hospitalization (18.5%), then PMD (18%). LE decreased an average of 6.7% for each standard deviation on the symptoms of infections scale. Although the percentage of lost LE is high for some conditions, 29.8% of participants reported no risk factors and 43.4% reported only one risk factor (table 4). Chronic PUs and amputation, associated with the greatest lost LE, were only reported by 2.7% and 2.1% of the participants, respectively.

Table 3.

Life expectancies as a function of health status for a hypothetical case at ages 20, 40, and 60.

Health Condition LE-20YO % LE
LOST*
LE-40YO % LE
LOST*
LE-60YO % LE
LOST*
Avg LE
LOST

No health conditions 45.59 28.67 14.17
Pressure Ulcers
 Non-chronic 40.76 10.6 % 24.72 13.8 % 11.43 19.3 % 14.6%
 Chronic 26.65 41.5 % 14.40 49.8 % 5.72 59.6 % 50.3%
Probable Major Depression 39.58 13.2 % 23.78 17.1 % 10.82 23.6 % 18.0%
1+ Hospitalizations 39.37 13.6 % 23.62 17.6 % 10.72 24.4 % 18.5%
Amputation 33.02 27.6 % 18.83 34.3 % 7.90 44.3 % 35.4%
Infections (>1 s.d.) 43.42 4.8 % 26.87 6.3 % 12.90 9.0 % 6.7%

NOTE: example is for a male, with non-cervical, non-ambulatory SCI

*

Percentage of lost life expectancy due to the presence of the condition.

Table 4.

Percentage of participants affected by specific health factors.

Behaviors Percentage
No conditions 29.82
Pressure Ulcers
 Non-chronic 53.98
 Chronic 2.66
Probable Major Depression 23.48
1+ Hospitalizations 6.86
Amputation 2.14
Infections Symptoms (>1 s.d.) 18.34
Multiple Conditions
 1 condition only 43.44
 2 conditions 18.34
 3 conditions 6.34
 4 conditions 1.97
 5 conditions 0.09
*

sum of the # of conditions.

Discussion

The results underscore the profound effects of secondary health conditions on LE after SCI. Whereas previous research had indicated only a modest effect of health on LE,4,13 the current study suggests substantial lost LE related to several factors. The differences between studies are likely attributable, at least in part, to the data sets utilized. Previous studies were largely based on analysis of NSCISC data, which is limited to a more circumspect number of predictors.

The presence of even a single secondary condition should be considered a threat to LE, with chronic PUs and amputations being particularly problematic. Other secondary health conditions, including infections and clinical depression, are also of concern. The presence of all cause hospitalization was also related to diminished LE, even though the interval between data collection and determination of mortality was 10 years (, i.e., hospitalization in the 12 months prior to data collection predicted mortality 10 years later). The pattern of predictors suggests there is likely an overall pattern of diminished health manifested through several secondary conditions, ultimately leading to a heightened risk of mortality and diminished LE. These findings are generally consistent with the existing literature in terms of risk of mortality. There has been insufficient literature on LE from which to draw comparisons.

Although declines in LE associated with secondary conditions were profound, not all participants reported risk factors (29.8% reported no conditions), and another 43.4% reported only 1 condition. Therefore, risk of diminished LE was focused on a subset of participants. Furthermore, the frequency of occurrence of the most important risk factors was rare, as chronic PUs and amputations were reported by less than 3% of the sample. Although non-chronic PUs were more common (54%), the amount of lost LE was substantially less (14.6%) when compared with chronic PU (50.3%).

Several important methodologic considerations are in this study. First, the health risk factors not only vary in terms of their prevalence and association with LE but also in their nature. For instance, amputations are permanent and likely relate to additional chronic conditions, such as diabetes. Although not truly permanent, chronic PUs was defined by essentially having PUs all the time. This is different than how other variables were measured, such as scores consistent with a diagnosis of depression at the time of the study or hospitalization for symptoms of infection within the previous 12 months. Therefore, the nature of the measurement of the variable itself may affect the LE, with the more permanent or chronic measures associated with more diminished LE. Had we been able to reliably measure depression, hospitalization, and symptoms of infection over time, it is almost certain those with chronic levels of these conditions would report greater diminished LE.

Clinical Implications

There are many ways the current findings can be translated into clinical practices. The identification of the predictorswill allow clinicians from multiple disciplines to assess risk for mortality quickly and efficiently. A minimum intervention for any clinician is to share information with the individual who has SCI. Clinicians may utilize the information on the specific risk factors to develop interventions in their own area of expertise. For instance, rehabilitation psychologists should ensure assessments for depression are routine upon outpatient visits and those at high risk for depression are identified and appropriate follow-up is implemented. Reviewing history of infections upon outpatient visits is also important. Other types of assessment, such as skin integrity, are almost certainly more routine. Interventions need to be developed targeting stakeholders more directly by disseminating information to them which may be utilized to promote self-health. Those with SCI certainly know chronic PUs lead to declining health, but knowing the extent to which they result in diminished LE may be more likely to lead to changes in health behaviors.

Study Limitations

There are several study limitations. First, the participant cohort was drawn after the onset of SCI, so substantial mortality could have occurred prior to enrollment. This may affect the absolute LE but would not likely affect the strength of a predictor factor. If so, it would probably diminish the apparent significance of a predictor. Second, there was a 10-year interval between prospective data collection and determination of mortality status, such that health factors may have changed substantially over time. This also may result in underestimating their relationships with mortality, particularly for variables not measured over time (i.e. depression) or only over a relatively short period of time (i.e. hospitalizations, infections). Third, all data were self-report. Although we do not anticipate this as highly problematic given the basic nature of their reporting of variables, any discrepancy of self-report with real status of the variables would result in an underestimate of the true relationships with mortality, and data from self-report and medical records may produce different results.25 Fourth, we utilized proxy variables for classification of injury severity (use of ambulatory status rather than ASIA grades), and this could have resulted in some differences in absolute LE (i.e., the true relationship of injury severity with mortality may have been underestimated). Fifth, although the NDI is highly accurate, failure to identify any deaths would have artificially inflated LE estimates. However, this would not necessarily result in different patterns of relationships between risk factors and mortality. Sixth, life expectancy estimates are averages. True life expectancy may vary substantially between individuals based on additional characteristics not accounted for in this study. Seventh, the study results are based on data from only one specialty hospital in the Southeastern United States. Lastly, the sample size was large compared with the majority of studies, but still smaller than those using NSCISC data. “Although the initial response rate was high (72%), attrition and enrollment could be selective (e.g., people in poor health less likely to respond).

Future Research

Ongoing research is needed to incorporate more frequent assessments of risk and protective factors and incorporate additional parameters, including biomarkers of stress, age, and vascular health. These assessments should take place over intervals longer than 10 years. Quality of life indicators also need to be incorporated into the model, as they were among the first factors to be identified in association with mortality.2628 We need to identify the underlying mechanisms for the observed findings, as we do not know whether these factors were significant by virtue of being indicators of overall health, or whether the physiologic processes related to amputations actually contribute to premature mortality. Lastly, investigation of an expanded set of risk and protective factors in association with causes of death would dramatically enhance our understanding of premature mortality and guide intervention strategies to promote greater longevity.

Conclusions

Several secondary health conditions represent risk factors for mortality and diminished LE after SCI. Health care providers should take the presence of 1 or more of these factors as an indicator of the need for intervention. Early intervention could potentially lengthen LE.

Acknowledgments

Sponsorship: The contents of this publication were developed under grants from the Department of Education, NIDRR grant numbers H133G050165, H133N50022, and H133B090005, and the National Institutes of Health, grant number 1R01 NS 48117. However, those contents do not necessarily represent the policy of the Department of Education or NIH, and you should not assume endorsement by the Federal Government.

We certify that no party having a direct interest in the results of the research supporting this article has or will confer a benefit on me or on any organization with which we are associated AND, if applicable, we certify that all financial and material support for this research (eg, NIH or NHS grants) and work are clearly identified in the title page of the manuscript.

List of Abbreviations

ASIA

American Spinal Injury Association

CHART

Craig Handicap Assessment Reporting Technique

CI

confidence interval

LE

life expectancy

NDI

National Death Index

NSCISC

National Spinal Cord Injury Statistical Center

OAHMQ

Older Adult Health and Mood Questionnaire

OR

odds ratio

PMD

probable major depression

PU

pressure ulcer

SCI

spinal cord injury

Footnotes

Reprints are not available from this author.

Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

References

  • 1.NSCISC. Annual Statistical Report. Birmingham, AL: University of Alabama; Nov, 2009. [Google Scholar]
  • 2.DeVivo MJ, Krause JS, Lammertse DP. Recent trends in mortality and causes of death among persons with spinal cord injury. Arch Phys Med Rehabil Nov. 1999;80(11):1411–1419. doi: 10.1016/s0003-9993(99)90252-6. [DOI] [PubMed] [Google Scholar]
  • 3.Strauss DJ, DeVivo MJ, Paculdo DR, Shavelle RM. Trends in life expectancy after spinal cord injury. Arch Phys Med Rehabil. 2006;87:1079–1085. doi: 10.1016/j.apmr.2006.04.022. [DOI] [PubMed] [Google Scholar]
  • 4.Krause JS, DeVivo MJ, Jackson AB. Health status, community integration, and economic risk factors for mortality after spinal cord injury. Arch Phys Med Rehabil. 2004;85:1764–1773. doi: 10.1016/j.apmr.2004.06.062. [DOI] [PubMed] [Google Scholar]
  • 5.Krause JS. Secondary conditions and spinal cord injury: A model for prediction and prevention. Top Spinal Cord Inj Rehabil. 1996;2(2):217–227. [Google Scholar]
  • 6.Krause JS, Carter RE, Pickelsimer E, Wilson D. A prospective study of health and risk of mortality after spinal cord injury. Arch Phys Med Rehabil. 2008;89:1482–1491. doi: 10.1016/j.apmr.2007.11.062. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Krause JS, Carter RE, Pickelsimer E. Behavioral risk factors of mortality after spinal cord injury. Arch Phys Med Rehabil. 2009;90(1):95–101. doi: 10.1016/j.apmr.2008.07.012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Krause JS, Carter R, Zhai Y, Reed K. Psychologic factors and risk of mortality after spinal cord injury. Arch Phys Med Rehabil. 2009;90(4):628–633. doi: 10.1016/j.apmr.2008.10.014. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Krause JS, Carter RE. Risk of mortality after spinal cord injury: relationship with social support, education, and income. Spinal Cord. 2009;47(8):592–596. doi: 10.1038/sc.2009.15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Lidal I, Snekkevik H, Aamodt G, Hjeltnes N, Biering-Sorensen F, Stanghelle J. Mortality after spinal cord injury in Norway. J Rehabil Med. 2007;39(2):145–151. doi: 10.2340/16501977-0017. [DOI] [PubMed] [Google Scholar]
  • 11.Garshick E, Kelley A, Cohen SA, et al. A prospective assessment of mortality in chronic spinal cord injury. Spinal Cord. 2005;43(7):408–416. doi: 10.1038/sj.sc.3101729. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Krause JS, Zhai Y, Saunders LL, Carter RE. Risk of mortality after spinal cord injury: an 8-year prospective study. Arch Phys Med Rehabil. 2009;90(10):1708–1715. doi: 10.1016/j.apmr.2009.04.020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Strauss D, DeVivo M, Shavelle R, Brooks J, Paculdo D. Economic factors and longevity in spinal cord injury: a reappraisal. Arch Phys Med Rehabil. 2008;89(3):572–574. doi: 10.1016/j.apmr.2007.11.025. [DOI] [PubMed] [Google Scholar]
  • 14.Krause JS, Saunders LL, DeVivo M. Income and risk of mortality after spinal cord injury. Arch Phys Med Rehabil. doi: 10.1016/j.apmr.2010.09.032. in press. [DOI] [PMC free article] [PubMed]
  • 15.Krause JS, Saunders LL. Life expectancy estimates in the life care plan: Accounting for economic factors. J Life Care Plan. 2010;9(2):15–28. [PMC free article] [PubMed] [Google Scholar]
  • 16.Krause JS, Saunders LL. Risk of mortality and life expectancy after spinal cord injury: The role of health behaviors and participation. Top Spinal Cord Inj Rehabil. 2010;16(2):53–60. doi: 10.1310/sci1602-53. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17. [Accessed September 28, 2007.];National Death Index. http://www.cdc.gov/nchs/ndi.htm.
  • 18.Kemp BJ, Adams BM. The Older Adult Health and Mood Questionnaire: A measure of geriatric depressive disorder. J Ger Psychiat Neuro. 1995;8(3):162–167. doi: 10.1177/089198879500800304. [DOI] [PubMed] [Google Scholar]
  • 19.Craig A, Tran Y, Middleton J. Psychological morbidity and spinal cord injury: a systematic review. Spinal Cord. 2009;47(2):108–114. doi: 10.1038/sc.2008.115. [DOI] [PubMed] [Google Scholar]
  • 20.Krause JS, Saunders LL, Reed KS, Coker J, Zhai Y, Johnson E. Comparison of the Patient Health Questionnaire and the Older Adult Health and Mood Questionnaire for self-reported depressive symptoms after spinal cord injury. Rehabil Psychol. 2009;54:440–448. doi: 10.1037/a0017402. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Strauss D, Shavelle R, DeVivo MJ, Day S. An analytic method for longitudinal mortality studies. J Ins Med. 2000;32:217–225. [PubMed] [Google Scholar]
  • 22.Shavelle RM, DeVivo MJ, Strauss DJ, Paculdo DR, Lammertse DP, Day SM. Long-term survival of persons ventilator dependent after spinal cord injury. J Spinal Cord Med. 2006;29(5):511–519. doi: 10.1080/10790268.2006.11753901. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Hosmer DW, Lemeshow S. Applied logistic regression. 2. New York, New York: John Wiley and Sons; 2000. [Google Scholar]
  • 24.DeVivo MJ. Estimating life expectancy for use in determining lifetime costs of care. Top Spinal Cord Inj Rehabil. 2002;7(4):49–58. [Google Scholar]
  • 25.Jones MP, Bartrop R, Dickson HG, Forcier L. Concordance between sources of morbidity reports: Self-reports and medical records. Frontiers in Pharmacology. 2011:2. doi: 10.3389/fphar.2011.00016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Krause JS, Crewe NM. Prediction of long-term survival of persons with spinal cord injury: An 11 year prospective study. Rehabil Psychol. 1987;32:205–213. [Google Scholar]
  • 27.Krause JS, Saari JM, Dykstra D. Quality of life and survival after spinal cord injury. SCI Psychosocial Process. 1990;3:4–8. [Google Scholar]
  • 28.Krause JS. Survival following spinal cord injury: A fifteen-year prospective study. Rehabil Psychol Sum. 1991;36(2):89–98. [Google Scholar]

RESOURCES