Abstract
BACKGROUND:
Malnutrition is common in elderly and is a risk factor for pressure ulcers.
AIM:
The aim of the present study was to determine the prevalence of malnutrition in geriatric and palliative patients hospitalised in long-term care facility, and to examine the influence of nutritional status on the prevalence of pressure ulcers (PU).
MATERIAL AND METHODS:
Descriptive, observational and cross-sectional study including 2099 patients admitted to the Hospital during a 24 month period (January 2013 to December 2014). We recorded: demographic data, body mass index (BMI), Braden score, laboratory parameters of interest (albumin, total protein, RBC count, haemoglobin and iron levels) and presence or absence of malnutrition and pressure ulcers.
RESULTS:
The pressure ulcer prevalence was 12.9% (256 out of 2099). Based on the BMI classification, 61.7% of patients had a good nutritional status, 27.4% were undernourished, and 2.1% were considered malnourished. Nutritional status was statistically significantly different between patients with and without PU (p < 0.0001). This study also showed that hypoproteinemia, hypoalbuminemia, low RBC was positively associated with PU prevalence.
CONCLUSION:
The results highlight the impact of nutritional status on the prevalence of pressure ulcers in hospitalised geriatric and palliative population. It is of paramount importance to correctly evaluate the presence of malnutrition in patients at risk of pressure ulcers.
Keywords: malnutrition, pressure ulcers, geriatric patients, palliative patients, long-term care facility
Introduction
A pressure ulcer (PU) is localised injury to the skin and/or underlying tissue usually over a bony prominence, as a result of pressure or pressure in combination with shear. It leads to ischemia, progressive destruction and necrosis of the underlying soft tissues [1]. Pressure ulcers are debilitating chronic wounds, which occur in people with advanced age, physical or cognitive impairments, and multiple comorbidities. It is a common problem among older adults in all health care settings [2].
The prevalence of PUs in long-term settings ranges from 11 to 29% [3-6]. Development of PU in hospitalised elderly patients is complex and multifactorial. Predisposing factors are classified as intrinsic (e.g. activity or mobility limitation, altered consciousness, abnormalities in nutritional status, comorbidities, ageing skin) or extrinsic (e.g., pressure, friction, shear, incontinence).
Malnutrition is a very common problem that affects approximately 30-50% of hospitalised patients. It is estimated that at least one-third of patients has some degree of malnutrition upon admission to the hospital (7). Additionally, among patients who are not malnourished upon admission, about one third may become malnourished while in the hospital (8). Among the elderly residents of long-term care institutions, the prevalence of in-hospital malnutrition has been estimated to be between 12.5 and 78.9% in different studies [9-11]. Overall, 50% of the residents require an individualised nutritional care plan [9].
Hospital malnutrition is associated with an increase in morbidity, mortality, a higher readmission rate, functional disabilities and physical complications, and, therefore, higher healthcare costs. Malnutrition is closely related to frailty, a clinical syndrome characterised by increased vulnerability to adverse health outcomes including acute illness, the decline in physiological reserve, and increased risk for disability, falls, hospitalisation, need for long-term care, and death [12].
The principal objective of this study was to assess the prevalence of malnutrition in elderly patients hospitalised in the long-term care facility. The secondary objective was to examine the influence of malnutrition on the prevalence of pressure ulcers.
Material and Methods
This observational study was carried out at the Geriatric and Palliative Care Hospital “13 November” in Skopje, Macedonia, the largest specialised geriatric and palliative hospital in the country that attends to patients through the Public Health System. The study design was approved by the Hospital Ethics Committee. Informed consent was waived because of the study’s observational nature.
Consecutive patients admitted to the hospital were enrolled from January 2013 to December 2014. We collected data using a case report form and recorded information about demographics, main diagnosis, BMI, laboratory findings, the presence of PU and PU characteristics.
Body mass index (BMI) was calculated using the formula: weight in kilogrammes/height in meters2. Using BMI classification, patients were classified as severely underweight, underweight, normal weight, overweight, severely obese or morbidly obese.
The Braden scale was used to assess the risk of developing PUs. The total score can range from 6 to 23 with a lower score indicating a higher risk [13].
The risk for PU development was assigned according to the stratification determined by the scale, into four groups; according to the Braden score [13]. The risk of PUs increases in patients with a score ≤ 12 points. The grading system of the EPUAP (European Pressure Ulcer Advisory Panel) was used [1].
Descriptive statistics was used to describe the study population, with continuous outcomes summarised as a mean and range, and categorical outcomes presented as a percentage. Chi-square test was used to analyse categorical variables. Independent t-test was used to analyse continuous variables. P-values < 0.05 were considered statistically significant.
Results
During the study period, two thousand and ninety-nine patients were consecutively admitted. Baseline characteristics of the study population are shown in Table 1. One thousand eight hundred and forty-three patients without PU (724 male and 1119 female, mean age 76.32 years, SD 11.192, range 22-103 years), and 256 patients with PU (86 male and 170 female, mean age 76.38, SD 11.296, range 37-97 years) participated in the study. No statistically significant difference was noted regarding age between the groups (p = 0.80).
Table 1.
Baseline characteristics of patient population, according to the presence/absence of PU
GENDER | AGE | ||||
---|---|---|---|---|---|
N (%) | X̄ | SD | Min.-Max. | ||
PU absent | Male | 724 (39.28) | 74.63 | 11.697 | 25-103 |
Female | 1119 (60.71) | 77.41 | 10.717 | 22-101 | |
Total | 1843 (87.8) | 76.32 | 11.192 | 22-103 | |
PU present | Male | 86 (33.59) | 74.50 | 12.234 | 38-97 |
Female | 170 (66.4) | 77.34 | 10.702 | 37-95 | |
Total | 256 (12.19) | 76.38 | 11.296 | 37-97 | |
Total | 2099 (100) | 76.32 | 11.202 | 22-103 |
Braden score ranged from 6 to 23 (mean 13.64, SD 3.247) and 1948 (92.8%) had a risk for pressure ulcers (Table 2).
Table 2.
Patient’s level of risk for development of PUs according to the Braden Scale (BS)
Level of risk | N | % |
---|---|---|
High (BS ≤ 12) | 913 | 43.5 |
Moderate (BS 13-14) | 478 | 22.8 |
Low risk (BS 15-19) | 557 | 26.5 |
No risk (BS ≥ 20) | 151 | 7.2 |
Total | 2099 | 100 |
Table 3 shows the distribution of patients according to the nutritional status. Based on the BMI classification, 61.7% of patients had a good nutritional status, 27.4% were undernourished, and 2.1% were considered malnourished. Nutritional status was statistically significantly different between patients with and without PU (χ2 = 25.350; p < 0.0001).
Table 3.
Differences in nutritional status between patients with (n = 256) and without a pressure ulcer (n = n=1843)
BMI classification | BMI | PU absent N (%) | PU present N (%) | Total N (%) |
---|---|---|---|---|
Severely underweight | 15-16 | 29 (1.57) | 16 (6.25) | 45 (2.1) |
Underweight | 16-18.5 | 501 (27.18) | 74 (28.9) | 575 (27.4) |
Normal weight | 18.5–24.9 | 1151 (62.45) | 144 (56.25) | 1295 (61.7) |
Overweight | 25.0–29.9 | 102 (5.53) | 12 (4.68) | 114 (5.4) |
Severely obese | 30.0–34.9 | 59 (3.2) | 10 (3.9) | 69 (3.3) |
Morbidly obese | >35 | 1 (0.05) | 0 | 1 (0.05) |
Total | 1843 (87.81) | 256 (12.19) | 2099 |
Table 4 shows nutrition-related laboratory values, according to the presence of PU. We detected a significant difference in presence of hypoalbuminemia (p < 0.0001), hypoproteinemia (p = 0.019), low RBC (p = 0.004) and low hemoglobin levels (p < 0.0001) in patients with PU, compared to patients without PU. Iron and triglyceride levels were not related to the presence of PU.
Table 4.
Nutrition-related laboratory values
PU absent | PU present | χ2 | p | |
---|---|---|---|---|
N (%) | N (%) | |||
↓ RBC count | 755 (40.96) | 131 (51.17) | 11.124 | 0.004 |
↓ Hemoglobin level | 1050 (57.36) | 186 (72.94) | 27.156 | <0.0001 |
↓ Iron (serum) | 1 (0.07) | 1 (0.5) | 2.48 | 0.289 |
↓ Total protein | 1194 (71.71) | 197 (78.8) | 5.495 | 0.019 |
↓ Albumin | 704 (48.55) | 175 (70.28) | 40.184 | <0.0001 |
↑Triglyceride level | 220 (14.58) | 34 (14.78) | 0.006 | 0.938 |
Discussion
In this retrospective study involving 2099 geriatric and palliative patients in a long-term setting, the following variables were significantly more frequently documented in patients with PU compared to those without PU: malnutrition measured as BMI, hypoproteinemia, hypoalbuminemia and anaemia (p < 0.05 for all).
Figure 1.
Percentage of patients with altered nutrition-related lab values
Malnutrition is defined as a state of nutrition in which a deficiency or excess of energy, protein and other nutrients causes measurable effects both on tissue/body structure and function [14].
The causes of malnutrition are multiple and complex [15]. In elderly patients, malnourishment may result from a combination of factors, including cardiac failure, difficulty chewing, dysphagia inflammatory illness, respiratory problems, reduced sense of smell and taste, and medications [16]. Furthermore, chronic diseases and cancer cause inflammation and increased cytokine production, which suppresses appetite. Acute and chronic infections, wounds, and hypermetabolism cause increased the need for energy and protein [17, 18]. Monotony of diet in institutional care, the timing of meals, decreased taste thresholds and a loss of olfactory distinction also impact nutritional wellness [19].
Malnutrition has numerous effects, including impaired collagen synthesis, and immune function. Wound healing refers to the complex and dynamic process of restoring cellular structures and tissue layers. In each phase of wound healing, poor nutritional status can delay the healing process or cause inadequate healing when nutritional deficiencies are not corrected [20, 21].
A number of studies have demonstrated that the relationship between malnutrition and pressure ulcers is bidirectional [22-24]. A direct correlation between malnutrition severity and the pressure ulcers has been reported [24].
Patients with chronic PUs - wounds that remain unhealed for more than six weeks - experience a continuous cycle in which they lose protein through excess exudate, resulting in delayed wound healing.
Our results revealed marked hypoproteinemia and hypoalbuminemia in patients with PUs. Protein-energy malnutrition reduces fibroblastic cellular activity and delays angiogenesis in the proliferative stage and reduced collagen synthesis and maturation in the remodelling stage, leading to increased wound dehiscence. Furthermore, proteins are lost in wound exudates, which can contain as much as 100 g of protein per day [25]. A deficiency in serum albumin causes impaired wound perfusion, reducing the osmotic pressure in the intravascular space. This causes interstitial oedema, reducing tissue oxygenation and tissue tolerance to the forces of pressure. Oedema also may be a factor in unidentified malnutrition by masking muscle and fat loss [26].
Older people are at risk of malnutrition if they have a BMI below 24, and malnutrition is indicated by a BMI of less than 20 [27]. The World Health Organization categorises underweight as BMI < 18.5. However, BMI may be unreliable in the presence of confounding factors such as oedema or ascites, and may not identify significant unintentional weight loss if used as a single assessment. Reliable measurement of height can be difficult in the elderly because of vertebral compression, loss of muscle tone and postural changes [28].
Malnutrition in a hospital setting may be prevented by using strategies that include assisting patients into a position conducive to swallowing safely and comfortably; implementing food charts to ensure accurate documentation of intake; and using fluid charts to record input and output to calculate fluid balance [21].
Maintaining nutritional status and preventing malnutrition aims to ensure that energy, protein and other micronutrients are available to prevent pressure ulcer development. No biochemical marker on its own offers a satisfactory screening test for malnutrition. Serum proteins synthesised by the liver have been used as markers of nutrition—albumin, transferrin, retinol-binding protein and thyroxine-binding albumin. Serum albumin has been most widely adopted; however, the long half-life of albumin means that serum albumin does not respond to short-term changes in protein and energy intake.
Nutrition and hydration play an important role in preserving skin and tissue viability and in supporting tissue repair for PU healing [29].
In the older population, undernutrition rather than overnutrition is the main cause for concern [30]. Malnourished older people are at increased risk of falls, lengthy hospital stays and rehabilitation, institutionalisation, postoperative complications, infections, pressure ulcers, poor wound healing, impaired muscle and respiratory function and death [31]. Unfortunately, malnutrition continues to be under-recognized in many hospitals [32].
Pressure ulcers are debilitating chronic wounds. Prevention of PUs in hospitalised elderly patients is an important health priority, one that requires clear identification of risk factors. Effective management of malnutrition requires collaboration among multiple clinical disciplines and all members of the clinical team [33].
In conclusion, malnutrition is a problem of high prevalence and impact in geriatric and palliative patients. Given the high prevalence of malnutrition among patients with pressure ulcers, performing a routine nutritional screening should result in early identification of residents with the risk of development of pressure ulcer.
Footnotes
Competing Interests: The authors have declared that no competing interests exist.
References
- 1.European Pressure Ulcer Advisory Panel, National Pressure Ulcer Advisory Panel, Pan Pacific Pressure Injury Alliance. Prevention and Treatment of Pressure Ulcers: Quick Reference Guide. Washington, DC: National Pressure Ulcer Advisory Panel; 2009. [Google Scholar]
- 2.Allman RM. Pressure ulcer prevalence, incidence, risk factors, and impact. Clin Geriatr Med. 1997;13(3):421–36. PMid:9227937. [PubMed] [Google Scholar]
- 3.Horn SD, Bender SA, Ferguson ML, Smout RJ, Bergstrom N, Taler G, Cook AS, Sharkey SS, Voss AC. The National Pressure Ulcer Long-Term Care Study: pressure ulcer development in long-term care residents. J Am Geriatr Soc. 2004;52(3):359–67. doi: 10.1111/j.1532-5415.2004.52106.x. http://dx.doi.org/10.1111/j.1532-5415.2004.52106.x . PMid:14962149. [DOI] [PubMed] [Google Scholar]
- 4.Donini LM, De Felice MR, Tagliaccica A, De Bernardini L, Cannella C. Comorbidity, frailty, and evolution of pressure ulcers in geriatrics. Med Sci Monit. 2005;11(7):CR326–36. PMid:15990690. [PubMed] [Google Scholar]
- 5.Lahmann NA, Halfens RJ, Dassen T. Pressure ulcers in German nursing homes and acute care hospitals: prevalence, frequency, and ulcer characteristics. Ostomy Wound Manage. 2006;52(2):20–33. PMid:16464992. [PubMed] [Google Scholar]
- 6.Neloska L, Damevska K, Nikolchev A, Pavleska L, Petreska-Zovic B, Kostov M. The influence of comorbidity on the prevalence of pressure ulcers in geriatric patients. Glob Dermatol. 2016;3(3):319–322. http://dx.doi.org/10.15761/GOD.1000183 . [Google Scholar]
- 7.Barker LA, Gout BS, Crowe TC. Hospital malnutrition: Prevalence, identification and impact on patients and the healthcare system. Int J Environ Res Public Health. 2011;8(2):514–527. doi: 10.3390/ijerph8020514. http://dx.doi.org/10.3390/ijerph8020514 . PMid:21556200 PMCid: PMC3084475. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Braunschweig C, Gomez S, Sheean PM. Impact of declines in nutritional status on outcomes in adult patients hospitalized for more than 7 days. J Am Diet Assoc. 2000;100(11):1316–22. doi: 10.1016/S0002-8223(00)00373-4. http://dx.doi.org/10.1016/S0002-8223(00)00373-4 . [DOI] [PubMed] [Google Scholar]
- 9.Pezzana A, Cereda E, Avagnina P, Malfi G, Paiola E, Frighi Z, Capizzi I, Sgnaolin E, Amerio ML. Nutritional Care Needs in Elderly Residents of Long-Term Care Institutions: Potential Implications for Policies. J Nutr Health Aging. 2015;19(9):947–54. doi: 10.1007/s12603-015-0537-5. http://dx.doi.org/10.1007/s12603-015-0537-5 . PMid:26482698. [DOI] [PubMed] [Google Scholar]
- 10.Lelovics Z. [Nutritional status and nutritional rehabilitation of elderly people living in long-term care institutions] Orv Hetil. 2009;150(44):2028–36. doi: 10.1556/OH.2009.28723. http://dx.doi.org/10.1556/OH.2009.28723 . PMid:19861289. [DOI] [PubMed] [Google Scholar]
- 11.Lou MF, Dai YT, Huang GS, Yu PJ. Nutritional status and health outcomes for older people with dementia living in institutions. J Adv Nurs. 2007;60(5):470–7. doi: 10.1111/j.1365-2648.2007.04442.x. http://dx.doi.org/10.1111/j.1365-2648.2007.04442.x . PMid:17973710. [DOI] [PubMed] [Google Scholar]
- 12.Gielen E, Verschueren S, O’Neill TW, Pye SR, O’Connell MD, Lee DM, et al. Musculoskeletal frailty: a geriatric syndrome at the core of fracture occurrence in older age. Calcif Tissue Int. 2012;91(3):161–77. doi: 10.1007/s00223-012-9622-5. http://dx.doi.org/10.1007/s00223-012-9622-5 . PMid:22797855. [DOI] [PubMed] [Google Scholar]
- 13.Bergstrom N, Braden B, Kemp M, Champage M, Ruby E. Predicting pressure ulcer risk: a multisite study of the predictive validity of the Braden Scale. Nurs Res. 1998;47:261–9. doi: 10.1097/00006199-199809000-00005. http://dx.doi.org/10.1097/00006199-199809000-00005 . PMid:9766454. [DOI] [PubMed] [Google Scholar]
- 14.Abbasi AA, Rudman D. Observations on the prevalence of protein-calorie undernutrition in VA nursing homes. J Am Geriatr Soc. 1993;41(2):117–21. doi: 10.1111/j.1532-5415.1993.tb02043.x. http://dx.doi.org/10.1111/j.1532-5415.1993.tb02043.x . [DOI] [PubMed] [Google Scholar]
- 15.Saunders J, Smith T. Malnutrition: causes and consequences. Clin Med (Lond) 2010;10(6):624–7. doi: 10.7861/clinmedicine.10-6-624. http://dx.doi.org/10.7861/clinmedicine.10-6-624 . [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Brownie S. Why are elderly individuals at risk of nutritional deficiency? Int J Nurs Pract. 2006;12(2):110–8. doi: 10.1111/j.1440-172X.2006.00557.x. http://dx.doi.org/10.1111/j.1440-172X.2006.00557.x . PMid:16529597. [DOI] [PubMed] [Google Scholar]
- 17.Norman K, Pichard C, Lochs H, Pirlich M. Prognostic impact of disease-related malnutrition. Clin Nutr. 2008;27(1):5–15. doi: 10.1016/j.clnu.2007.10.007. http://dx.doi.org/10.1016/j.clnu.2007.10.007 . PMid:18061312. [DOI] [PubMed] [Google Scholar]
- 18.Donini LM, Savina C, Cannella C. Eating habits and appetite control in the elderly: the anorexia of aging. Int Psychogeriatr. 2003;15(1):73–87. doi: 10.1017/s1041610203008779. http://dx.doi.org/10.1017/S1041610203008779 . PMid:12834202. [DOI] [PubMed] [Google Scholar]
- 19.Harris CL, Fraser C. Malnutrition in the institutionalized elderly: the effects on wound healing. Ostomy Wound Manage. 2004;50(10):54–63. PMid:15509882. [PubMed] [Google Scholar]
- 20.Todorovic V. Food and wounds: nutritional factors in wound formation and healing. Br J Community Nurs. 2002;43-4:46. doi: 10.12968/bjcn.2002.7.sup2.12981. 48 passim. http://dx.doi.org/10.12968/bjcn.2002.7.Sup2.12981 . PMid:12362158. [DOI] [PubMed] [Google Scholar]
- 21.Smoliner C, Norman K, Scheufele R, Hartig W, Pirlich M, Lochs H. Effects of food fortification on nutritional and functional status in frail elderly nursing home residents at risk of malnutrition. Nutrition. 2008;24(11-12):1139–44. doi: 10.1016/j.nut.2008.06.024. http://dx.doi.org/10.1016/j.nut.2008.06.024 . PMid:18789649. [DOI] [PubMed] [Google Scholar]
- 22.Günes ÜY, Efteli E. Predictive validity and reliability of the Turkish version of the risk assessment pressure sore scale in intensive care patients: results of a prospective study. Ostomy Wound Manage. 2015;61(4):58–62. PMid:25853378. [PubMed] [Google Scholar]
- 23.Fossum M, Ehnfors M, Svensson E, Hansen LM, Ehrenberg A. Effects of a computerized decision support system on care planning for pressure ulcers and malnutrition in nursing homes: an intervention study. Int J Med Inform. 2013;82(10):911–21. doi: 10.1016/j.ijmedinf.2013.05.009. http://dx.doi.org/10.1016/j.ijmedinf.2013.05.009 . PMid:23827767. [DOI] [PubMed] [Google Scholar]
- 24.Park KH. A retrospective study using the pressure ulcer scale for healing (PUSH) tool to examine factors affecting stage II pressure ulcer healing in a Korean acute care hospital. Ostomy Wound Manage. 2014;60(9):40–51. PMid:25211606. [PubMed] [Google Scholar]
- 25.Russell L. The importance of patient’s nutritional status in wound healing. B J Nurs. 2001;10(6S):S42–49. doi: 10.12968/bjon.2001.10.Sup1.5336. http://dx.doi.org/10.12968/bjon.2001.10.Sup1.5336 . PMid:12070399. [DOI] [PubMed] [Google Scholar]
- 26.James J. Optimal wound healing: a comprehensive approach through metabolic, anabolic and nutritional interventions. Involuntary weight loss and its effect on the body to heal. WOUNDS. 2002;14(9):4–8. [Google Scholar]
- 27.Mathus-Vliegen EM. Old age, malnutrition, and pressure sores: an ill-fated alliance. J Gerontol A Biol Sci Med Sci. 2004;59(4):355–60. doi: 10.1093/gerona/59.4.m355. http://dx.doi.org/10.1093/gerona/59.4.M355 . PMid:15071079. [DOI] [PubMed] [Google Scholar]
- 28.Balcombe NR, Ferry PG, Saweirs WM. Nutritional status and well being. Is there a relationship between body mass index and the well-being of older people? Curr Med Res Opin. 2001;17:1–7. http://dx.doi.org/10.1185/03007990152005397 . PMid:11464440. [PubMed] [Google Scholar]
- 29.Posthauer ME, Banks M, Dorner B, Schols JM. The role of nutrition for pressure ulcer management: national pressure ulcer advisory panel, European pressure ulcer advisory panel, and pan pacific pressure injury alliance white paper. Adv Skin Wound Care. 2015;28(4):175–88. doi: 10.1097/01.ASW.0000461911.31139.62. http://dx.doi.org/10.1097/01.ASW.0000461911.31139.62 . PMid:25775201. [DOI] [PubMed] [Google Scholar]
- 30.Elia M, editor. Development and use of the ‘Malnutrition Universal Screening Tool’ (‘MUST’) for Adults. BAPEN; 2003. Screening for Malnutrition: A Multidisciplinary Responsibility. [Google Scholar]
- 31.Milne AC, Potter J, Avenell A. Protein and energy supplementation in elderly people at risk from malnutrition. Cochrane Database Syst Rev. 2005 Apr 18;(2):CD003288. doi: 10.1002/14651858.CD003288.pub2. Review. Update in: Cochrane Database Syst Rev 2009;(2): CD003288. PMid:19370584. [DOI] [PubMed] [Google Scholar]
- 32.Kirkland LL, Kashiwagi DT, Brantley S, Scheurer D, Varkey P. Nutrition in the hospitalized patient. J Hosp Med. 2013;8(1):52–58. doi: 10.1002/jhm.1969. http://dx.doi.org/10.1002/jhm.1969 . PMid:23065968. [DOI] [PubMed] [Google Scholar]
- 33.Tappenden KA, Quatrara B, Parkhurst ML, Malone AM, Fanjiang G, Ziegler TR. Critical role of nutrition in improving quality of care: an interdisciplinary call to action to address adult hospital malnutrition. J Parenter Enteral Nutr. 2013;37(4):482–97. doi: 10.1177/0148607113484066. http://dx.doi.org/10.1177/0148607113484066 . PMid:23736864. [DOI] [PubMed] [Google Scholar]