Original Article

Indications for percutaneous endoscopic gastrostomy and survival in old adults

Anna Malmgren1, Gunnel Wärn Hede2, Brita Karlström3, Tommy Cederholm4, Per Lundquist1,5, Mikael Wirén1,5 and Gerd Faxén-Irving6*

1Department of Surgical and Medical Gastroenterology and Hepatology, Karolinska University Hospital, Stockholm, Sweden; 2Department of Neurobiology, Care Sciences and Society, Division of Nursing, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden; 3Department of Food, Nutrition and Dietetics, Uppsala University, Uppsala, Sweden; 4Department of Public Health and Caring Sciences, Clinical Nutrition and Metabolism, Uppsala University, Uppsala, Sweden; 5Department of Clinical Sciences, Intervention and Technology (CLINTEC), Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden; 6Department of Neurobiology, Care Sciences and Society, Division of Clinical Nutrition, Karolinska Institutet, and Clinical Nutrition and Dietetics, Karolinska University Hospital, Stockholm, Sweden

Abstract

Background: Many diseases striking old adults result in eating difficulties. Indications for selecting individuals for percutaneous endoscopic gastrostomy (PEG) are unclear and everybody may not benefit from the procedure.

Objective: The aim of this study was to evaluate indications for and survival after PEG insertion in patients older than 65 years.

Design and Methods: A retrospective analysis including age, gender, diagnosis, indication, and date of death was made in 201 consecutive individuals, 94 male, mean age 79±7 years, who received a nutritional gastrostomy.

Results: Dysphagia was present in 86% of the patients and stroke was the most common diagnosis (49%). Overall median survival was 123 days and 30-day mortality was 22%. Patients with dementia and Mb Parkinson had the longest survival (i.e. 244 and 233 days), while those with other neurological diseases, and head and neck malignancy had the shortest (i.e. 75 and 106 days). There was no difference in mortality in patients older or younger than 80 years, except in patients with dementia.

Conclusions: Old age should not be a contraindication for PEG. A high 30-day mortality indicates that there is a need of better criteria for selection and timing of PEG insertion in the elderly.

Keywords: elderly; enteral nutrition; gastrostomy; mortality; PEG; survival

Received: 26 January 2011; Accepted: 23 June 2011; Published: 20 July 2011

Citation: Food & Nutrition Research 2011, 55: 6037 - DOI: 10.3402/fnr.v55i0.6037

Food & Nutrition Research 2011. © 2011 Anna Malmgren et al. This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License (http://creativecommons.org/licenses/by-nc/3.0/), permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.


Introduction

Many older patients have nutritional problems caused by eating difficulties that may be due to somatic diseases, frailty, or fatigue. When oral nutrition no longer is possible or sufficient, enteral nutrition (tube feeding) is an option especially in patients with a functional gastro-intestinal tract. Percutaneous endoscopic gastrostomy (PEG) is the preferential route when the treatment is expected to last for a longer period of time since it is associated with less treatment failures and better nutritional status than nasogastric tube feeding (NGT) (1). Moreover, the risk for complications is less with PEG than with NGT (1, 2). PEG was originally described for pediatric use (3), but is today the most common way of supplying artificial enteral nutrition also in adults including the elderly. The intent by using artificial enteral nutrition may be to increase quality of life or to prolong survival. However, many studies report 30-day mortality figures after placement of PEG of around 20% (48); that is, figures that would be unacceptable for any other surgical procedure both from a patient and a health-economical perspective. There is a need to find clinical variables that may facilitate the decision process in order to find the patients that may benefit most from the procedure. In a review, Mitchell and Tetroe (9) pointed out some factors that were related to increased mortality after PEG in patients older than 65 years, e.g. old age, malignancy, male gender, and hypoalbuminemia. A recent study from Blomberg et al. showed that low albumin, high CRP, age ≥65 years, and body mass index (BMI) <18.5 were associated with increased 30-day mortality after PEG insertion. Patients with a combination of low albumin and high CRP levels had a mortality rate of 20% compared with <3% in patients with normal values (10).

The aim of this study was to examine the indications and survival in a consecutive group of elderly individuals who had received PEG.

Methods

Data for this study was collected between November 2001 and June 2002. Included were all consecutive patients, 65 years or older, that underwent PEG insertion from January 1997 to December 2000 at the Endoscopy Unit at Karolinska University Hospital, Huddinge. A retrospective survey of four different patient chart systems was carried out and the last day for the follow-up was in April 2002. Data on diagnosis, indication for PEG, operating time, removal time, or time of death were collected. The PEG insertion was performed in the endoscopy suite using intravenous conscious sedation and local anesthesia. The pull procedure was used to place a 20 Fr silicon tube with a semirigid inner bumper under endoscopic control. Antibiotic prophylaxis (Cefuroxim) was administered intravenously prior to the procedure. Data of weight and height were not available. Thirteen patients that received their PEG for drainage of an obstruction or for medical supplementation were excluded. For one patient, the time of insertion of the PEG was not noted. In 10 of the remaining 201 patients, the date for removal of the PEG was not retrievable. After these exclusions, the survival analysis was calculated on 191 patients.

Statistics and ethics

Data are presented as mean (±SD) and median with range and 95% confidence intervals. For survival analysis we used the Log-rank test and Kaplan Meier curves (SPSS and Statistica software programs). The study followed local ethic considerations conformed to the Helsinki declaration.

Results

There were 201 patients, 65 years or older, that received a PEG for nutritional support between 1997 and 2000 at the Karolinska University Hospital, Huddinge, 107 males, 94 women with a mean age of 79 years (range 65–95). The patients were categorized into seven diagnosis groups: stroke, dementia, Mb Parkinson, other neurological diseases (mainly amyotrophic lateral sclerosis [ALS]), malignancies with or without dysphagia, and miscellaneous. Moreover, they were categorized into three main groups of indications: dysphagia, inability to eat (as a consequence of extreme weakness, motor and mobility problem, and fatigue due to the illness), and nutritional support (EN was used in combination to oral intake). Many patients had multiple diseases. Diagnoses of the patients and the indications for PEG are shown in Table 1. Stroke was the most common diagnosis (49%) and malignancies with dysphagia were the second most common (16%). In 86% of the patients dysphagia was the indication for PEG.


Table 1. Number of patients, age (±SD), and indications for PEG in the various diagnosis groups
All patients Stroke Dementia Mb Parkinson Other neurology. disorders Malignant esophageal obstruction Other malignancies Miscellaneous No data available
N (%) 201 97 49 16 (8) 12 (6) 13 (6) 33a (16) 5 (2) 23 (12) 2 (1)
Age, years 79±7 81±6 80.5±7 73±5 75±8 74±6 74±4 78±8
Females, n (%) 94 (47) 52 (54) 9 (56) 4 (33) 8 (62) 8 (24) 2 (40) 10 (43)
Indication for PEG (n,%)
Dysfagia 173 (86) 92 (95) 7 (44) 11 (92) 13 (100) 32 (97) 2 (40) 16 (70)
Inability to eat 12 (6) 5 (5) 2 (12.5) 1 (8) 0 0 1 (20) 3 (13)
Nutritional support 8 (4) 0 2 (12.5) 0 0 1 (3) 1 (20) 4 (17)
No data available 8 (4) 0 5 (31) 0 0 0 1 (20) 0 2
aCancer of esophagus (20), lung (3), pharynx (2), larynx (2), tonsils (2), mouth (2), thyroid (1), and vocal cords (1).

Median survival was 123 days with a range of 0–1713 days (Fig. 1). Survival in the various diagnosis groups is shown in Table 2. The 30-day mortality in the total patient population was 22% and the 90-day mortality was 42%. There were 44 and 33% of the patients that were still alive after 6 months and after 12 months, respectively. Patients with Mb Parkinson and dementia had the longest survival while the patients with other neurological diseases and malignant esophageal obstructions had the shortest, with a 1-year mortality of 77% (Table 2).


Fig 1

Fig. 1.  Survival time, all patients, n=191.


Table 2. Median survival in days and 1-,3-, 6-, and 12-month mortality for various diagnostic groups, n=191
Mortality (%)
Median survival in days (95% CI) Days
30 90 180 365
Dementia (n=16) 244 (49–439) 25 37 37 58
Mb Parkinson (n=11) 233 (0–660) 9 18 36 55
Miscellaneous (n=19) 130 (45–215) 17 39 61 61
Stroke (n=95) 119 (15–223) 22 46 55 67
Malignant obstruction (n=31) 106 (63–149) 23 42 68 77
Other neurological diseases (n=13) 75 (15–135) 23 54 62 77
Other malignancy (n=4)
No data available (n=2)
All patients (n=191) 123 (74–172) 22 42 56 67

When patients were dichotomized according to age over and under 80 years there was no difference in 1-year mortality in the whole group, i.e. 70 and 64%, respectively (ns). Except for patients with dementia, where the corresponding figure for 1-year mortality was 33 and 73%, respectively (p=0.025) there was no age-related difference in the various diagnostic subgroups (data not shown).

Twenty patients had their PEG removed after a mean of 300 days and a median of 200 days. Thirteen of these 20 patients were still alive at the time of the last follow-up in the year 2002.

Discussion

This retrospective survey over older patients that received PEG for nutritional treatment found a just stroke to be the most common diagnosis and dysphagia to be responsible for around 90% of the indications. Median survival was around 4 months.

Most studies on this subject include adults of all ages and the mean age is usually around 65 years. We report data from patients above 65 years. In the literature there seems to be little agreement on whether to report indication or diagnosis for a decision to place a PEG. The prognosis, treatment effect, and survival differed between the diagnoses. There were different indications for PEG insertion within each diagnoses and knowing the indication seems important for planning of medical and nursing resources needed after the hospital stay. In this study both indications and diagnoses are reported. Several of the findings confirm what others have reported regarding underlying disease, survival, and mortality. Neurological disease was the dominating cause for PEG insertion followed by malignancies in the upper GI tract (5, 11). In the study by Callahan on 150 elderly patients, 41% suffered from stroke, 35% had neuro-degenerative disorders, and 13% had cancer.

When it comes to survival it appears that results from the present study deviates from previous reports. This may reflect different treatment strategies. Not only the decision to start nutritional support by PEG, but also the timing of this decision in relation to the patients clinical status is of great importance for the survival outcome. In our study the median survival time was 123 days, which is shorter than usually presented. For example, in the study by Fisman et al. (6) the median survival was 210 days in 175 patients, all above 65 years of age. The 95 patients with stroke had a median survival of 119 days, which is less than half of the median survival time of 305 days reported by James et al. (12) in 126 patients with stroke and dysphagia and a similar mean age of 80 years. Such differences may reflect a tendency to decide on PEG insertion later in the disease process, rather than variations in the care of the patients after the surgical procedure. The effect of timing and method of enteral feeding for dysphagic stroke patients was studied in the FOOD trial (13). The authors concluded that early tube feeding might reduce case fatality but at the expense of increasing the proportion surviving with poor outcome. Therefore early initiation of PEG feeding was not supported (13). Since only those patients were enrolled in whom the responsible clinician was uncertain of the best feeding practice, the results from this multicentre trial have to be interpreted with caution.

The results from the FOOD trial and other studies on EN in stroke patients with dysphagia are reviewed and analyzed in the ESPEN guidelines on enteral nutrition for geriatric patients. Treatment with EN is recommended as soon as possible unless there are compelling reasons against it in patients with neurological dysphagia. For long-term nutritional support PEG should be preferred to NGT, since it is associated with less treatment failures and better nutritional status (1). Studies on the natural course of dysphagia after stroke show that spontaneous remission of the swallowing difficulty occurs 7–14 days after the acute event in 73%–86% of the patients (4, 14, 15). Intensive swallowing therapy is also recommended to accompany the treatment (1).

Requests for PEG in order to facilitate care are prevalent; that is, the staff in geriatric and elderly care institutions tend to prefer PEG to a temporary naso-gastric tube or to the time-consuming oral feeding. It has been reported that one-third of patients received a PEG due to demands from the community (16). Considerations like this may have implications for the survival length in populations with PEG.

Dementia is a diagnosis where the benefits of placing a PEG are questioned. The decision to place a PEG in a patient with dementia must be taken with ethical considerations (11, 1721). ESPEN guidelines do not recommend enteral nutrition to persons with severe dementia due to more risks than benefits for persons with severe dementia and only occasionally in early and moderate dementia to ensure adequate energy and nutrient supply and to prevent undernutrition (22). A Cochrane review by Sampson et al. confirmed this and concluded that there is insufficient evidence to suggest that enteral nutrition is beneficial in patients with advanced dementia (23). The 244 days of median survival does not support previous observations of a worsened prognosis for patients with dementia and this may reflect a tendency for selecting mainly mildly demented otherwise healthy patients for PEG insertion. The tripled short-term mortality in patients combining dementia and age above 80 years indicate that high age should be a precaution for the decision of PEG even in patients with milder forms of dementia.

A limitation in this survey is that we have no information about the patients’ cognitive status at the time when the PEG insertion took place. Further, our data do not allow any conclusions about quality of life for the patients that received PEG. To our knowledge no studies so far have addressed this question.

In accordance with previous reports, a diagnosis of malignancy carried a higher risk of short survival (6, 9, 24). However, the difference was less accentuated in the present study (106 vs. 130 days), when for example compared to a study by Fisman et al. (6) that reported a survival of 137 days in patients with malignant disease versus 321 days in patients with non-malignant disease. It should be acknowledged that PEG insertion due to malignant esophageal obstruction could be justified by palliative reasons even when survival is expected to be short.

Patients with ALS usually present with a long survival after PEG insertion (9, 25). In our study the 13 patients with ‘other neurological diseases’ (12 with ALS) had the shortest survival time of all. However, the current patients were notably older (75±8 years) compared to those presented by Mitchell and Tetroe (9) and Chio et al. (25) (60 and 62 years).

Not unexpectedly, patients older than 80 had a slightly worse prognosis than those younger than 80, i.e. in line with other reports (4, 2628). This age effect was most pronounced in the patients with dementia. Otherwise the age effect appeared so small that it would not be advisable to identify age as a clear unfavorable factor for PEG in this unselected consecutive group of elderly patients.

The overall 30-day mortality of 22% is well in accordance with published data (6, 29), whereas there are reports on even higher mortality figures of up to 28% (11, 30). The high short-term mortality in this elderly population may not be due to procedure-related complications, but rather to the decisions of PEG placement taken late in the disease course. The 90-day mortality of 42% and 180 day figure of 56% also corresponds well to published data of 44 and 52% (11). In the review by Tetroe and Mitchell (9) the 1-year mortality was 62%, well in line with our figure of 67% and other reports of 61 and 66% (9, 6, 30). Callahan et al. showed a 1-year mortality of 50% (5).

We may conclude that there is a major variability in survival after PEG insertion in elderly patients that suffer from various diseases. The high 30-day mortality of 22% in this study is in accordance with published data, but median survival time appeared to be shorter than previously reported. Dementia was not found to be a negative prognostic factor for survival in this population, especially not in those below the age of 80 years. However, the limited access to patient data, such as disease severity and nutritional state, does not allow a deeper analysis on which clinical variables, which would be discriminative for selecting patients, would benefit most from the procedure. According to the recent study by Blomberg et al., it should not be recommended to make PEG insertion in patients with CRP levels and low albumin indicating ongoing inflammation (10).

There is still an urgent need for developing ways to decide the risk/benefit ratio in the individual patient in order to optimize the timing and route of nutritional support. Especially in this field, ethical consideration is a challenge for the scientific approach, but such efforts would need prospective randomized controlled studies, which most likely are not accepted due to ethical considerations. However, future studies that include questions regarding quality of life are possible to perform and are needed to elucidate the ethical aspects of enteral nutrition treatment in geriatric patients.

Conflict of interest and funding

The authors have not received any funding or benefits from industry or elsewhere to conduct this study.

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*Gerd Faxen-Irving
Karolinska University Hospital
Huddinge
SE-141 86 Stockholm, Sweden
Tel: +(46) 8 58586071
Fax: +(46) 8 58580540
Email: gerd.faxen.irving@ki.se