Program to Diagnose Probability of Aspiration Pneumonia in Patients with Ischemic Stroke
Program to Diagnose Probability of Aspiration Pneumonia in Patients with Ischemic Stroke
Autores:
ARTIGO ORIGINAL
International Archives of Otorhinolaryngology
versão impressa ISSN 1809-9777versão On-line ISSN 1809-4864
Int. Arch. Otorhinolaryngol. vol.18 no.3 São Paulo 2014
http://dx.doi.org/10.1055/s-0034-1374646
Introduction
Stroke is a major cause of death and disability worldwide, with a strong economic and social impact. Approximately 40% of patients show motor, language, and swallowing disorders.1
Stroke causes neurogenic oropharyngeal dysphagia (NOD) that, besides limiting food intake, carries a greater risk of malnutrition and tracheal aspiration and triples the incidence of aspiration pneumonia.2 3 4 5 6 This higher risk is due to several factors, such as possibility of silent aspiration (without cough reflex) or microaspiration; motor dysfunction of the pharynx; delayed swallow initiation; presence of pharyngeal residues at epiglottic valleculae, pyriform sinuses, and/or posterior wall of the pharynx; and impairment of the laryngeal closure mechanism. The detection of such risks, in many situations, may require an alternative route for nutrition and hydration.7 NOD occurs in ∼25 to 90% of strokes,8 9 10 similar to the acute phase, when 45% of patients have swallowing disorders, often with tracheal aspiration.11
Tracheal aspiration is defined as the passage of saliva, fluid, or food in the subglottic region below the vocal folds.12 13 It is estimated that 50% of patients with tracheal aspiration will develop aspiration pneumonia.14
Attempting to help physicians better manage dysphagia after stroke, this study used a computer program, Nética Shell (Norsys, Vancouver, Canada),15 which uses Bayesian networks as a tool and shows results in a probabilistic form. Thus, the aim of this research is to evaluate the use of software to infer the probability of pneumonia in patients with ischemic stroke.
Methods
This was a prospective and cross-sectional study of 52 patients after ischemic stroke who were examined from March 2010 to August 2012, with 23 (44.2%) women and 29 (55.8%) men, with mean age of 62.05 ± 13.88 years. Patients were recruited in the emergency room at a university hospital in Curitiba and evaluated by a neurologist of the Neurology Department from the same institution. The diagnosis of ischemic stroke was confirmed clinically and by computed axial tomography.
The study included patients of both genders 18 years of age and older who had ischemic stroke according to clinical assessment and imaging study, confirmed by a neurologist, and who underwent clinical and instrumental evaluations of swallowing within the first 72 hours of onset of symptoms of ischemic stroke. The exclusion criteria were patients with a prior history of head and neck surgery, patients with structural abnormalities of oropharynx and larynx, those with a lowered level of consciousness with score less than 10 on the Glasgow Coma Scale,16 those clinically unstable, and patients who refused to sign the informed consent form.
The research consisted of two phases performed on the same day using clinical and flexible endoscopic evaluation of swallowing (FEES),17 18 with protocols used by the institution. During clinical swallow evaluation, the patient remained seated in reach of a cup, tablespoon, plastic syringe, and straw. The patient was then offered 5 mL, 10 mL, and free sip of each food consistency following American Dietetic Association standard without interruption between them.19 Then the Functional Oral Intake Scale (FOIS) was administered.18
For FEES,17 the consistencies offered were similar to those used in the preceding phase, but with the addition of aniline blue dye to contrast with pink mucosa. During FEES,17 patients were offered the same sequence of swallows as in the clinical swallow evaluation. In the presence of swallowing difficulty, laryngeal penetration, or tracheal aspiration, consistencies began to be arranged progressively or the examination stopped. The test was discontinued if the patient showed nausea, vomiting, or any clinical instability.
The data collected during the test included laryngeal sensitivity, presence of premature spillage, pharyngeal residue (posterior pharyngeal wall, epiglottic valleculae, pyriform sinuses), pharyngeal clearance (after three swallows), and laryngeal penetration or tracheal aspiration (with or no cough reflex). The Severity Scale for Dysphagia—Penetration Aspiration Scale was administered.20
Based on the findings of clinical and instrumental assessments (FEES),17 speech therapy guidance was conducted for the patient, caregiver, and/or family.
This research used the safe mode of Bayesian network Nética Shell (Norsys, Vancouver, Canada),15 available on the Internet without charge, and the variables were created based on a previous study.21 The following findings were used as variables: clinical swallow evaluation (oral diet, tube feeding, tracheostomy, level of consciousness, gag reflex, spontaneous swallow, larynx elevation, wet voice, and voluntary cough) and FEES (laryngeal sensitivity, premature spillage, pharyngeal residue and tracheal aspiration). Thereafter, the Bayesian network was used with the findings of phases 1 and 2 (Fig. 1) to investigate the probability of the patient developing aspiration pneumonia. Results were then divided into groups by percentage.
Fig. 1 Bayesian model (Gomes21).
All patients were followed by the author and the attending physician of the patient during the hospitalization period and fortnightly for 3 months.22
Statistical analysis was performed using descriptive methods, chi-square and difference in proportions tests, with a significance level of 0.05 (5%).
The study was approved by the Ethics Committee in Research of HC-UFPR under the number 2098.265/2009-11.
Results
Among the 52 patients, in the clinical swallow evaluation, 30 (57.5%) showed no clinical signs of tracheal aspiration such as coughing, wet voice, and dyspnea,23 and in instrumental evaluation FEES,17 34 (65.4%) showed no tracheal aspiration. There was no significant difference between the clinical swallow evaluation and FEES for the presence of tracheal aspiration (p = 0.4201),17 as shown in Table 1.
Table 1 Comparison of clinical and instrumental swallow evaluations for tracheal aspiration
| Tracheal aspiration | Evaluations | p | |
|---|---|---|---|
| Clinical | FEES | ||
| Absent | 30 (57.5%) | 34 (65.4%) | 0.4201 |
| Present | 22 (42.5%) | 18 (34.6%) | |
| Total | 52 (100.0%) | 52 (100.0%) | |
Abbreviation: FEES, flexible endoscopic evaluation of swallowing.
Of the 18 patients (34.6%) who had aspirated food consistencies during the examination, 14 patients (66.6%) had tracheal aspiration of pudding consistency, 12 (57.1%) of honey consistency, 13 (61.9%) of nectar consistency, and 17 (80.9%) of liquid consistency.
Regarding FOIS,24 13 (25.0%) of the patients were at level 1 (nothing by mouth), 1 (1.7%) patient was at level 2 (tube-dependent with minimal attempts of food or liquid), 1 (1.7%) patient was at level 3 (tube-dependent with consistent oral intake of food or liquid), 2 (4.0%) patients were at level 4 (total oral diet of a single consistency), 5 (9.5%) patients were at level 5 (total oral diet with multiple consistencies, but requiring special preparation or compensations), 2 (4.0%) patients were at level 6 (total oral diet with multiple consistencies without special preparation, but with specific food limitations), and 28 (53.9%) patients were at level 7 (total oral diet with no restrictions), as shown in Table 2.
Table 2 Distribution of patients in FOIS scale
| FOIS | Number of patients |
|---|---|
| 1 | 13 (25.0%) |
| 2 | 1(1.7%) |
| 3 | 1 (1.7%) |
| 4 | 2 (4.0%) |
| 5 | 5 (9.5%) |
| 6 | 2 (4.0%) |
| 7 | 28 (53.9%) |
| Total | 52 (100.0%) |
Abbreviation: FOIS, Functional Oral Intake Scale.
The Rosenbeck Scale20 showed no significant relationship between the scale and the presence or absence of pneumonia (p = 0.2293; Table 3).
Table 3 Relation between Rosenbek scale and aspiration pneumonia
| Aspiration pneumonia | Rosenbek scale | p | |||||||
|---|---|---|---|---|---|---|---|---|---|
| 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | ||
| Present | 0 | 0 | 1 | 0 | 0 | 0 | 1 | 1 | 0.2293 |
| Absent | 30 | 1 | 1 | 1 | 0 | 0 | 4 | 12 | |
To allow the difference in proportions test, groups were considered in two categories: 0 to 49% and 50 to 100%. Thus, difference in proportions test, with level of significance of 0.05, resulted in p < 0.001, that is, the proportion of patients in category 0 to 49% was significantly higher than in the category of 50 to 100% (Table 4).
Table 4 Number of patients by percentage groups of probability of pneumonia aspiration
| Software | p | |
|---|---|---|
| Groups by % probability of pneumonia | Number of patients | |
| 0–19% | 32 (61.7%) | |
| 20–49% | 5 (9.5%) | |
| 50–79% | 3 (5.7%) | <0.001 |
| 80–100% | 12 (23.1%) | |
| Total | 52 (100.0%) | |
Table 5 demonstrates the presence and absence of aspiration pneumonia within the group of patients with odds > 80% of having aspiration pneumonia and software variables. In the 3-month follow-up, only three patients had aspiration pneumonia; Table 6 shows the outcome shown since the stroke.
Table 5 Relation between aspiration pneumonia and patients with probability >80% for pneumonia
| Pneumonia | Probability 80–100% |
|---|---|
| Present | 3 (25.0%) |
| Absent | 9 (75.0%) |
| Total | 12 (100.0%) |
Table 6 Distribution of the outcome of three patients stricken by pneumonia
| n | Gender | Age (y) | FOIS | Rosenbek scale | FEES | Software % | Upshot |
|---|---|---|---|---|---|---|---|
| 1 | F | 86 | 7 | 3 | Laryngeal penetration | 85.20 | Decreased consciousness, pneumonia and death |
| 2 | M | 83 | 4 | 7 | Tracheal aspiration | 98.41 | Sepsis, pneumonia and death |
| 3 | M | 74 | 1 | 8 | Tracheal aspiration | 99.50 | Decreased consciousness, pneumonia, and death |
Abbreviations: FEES, flexible endoscopic evaluation of swallowing; FOIS, Functional Oral Intake Scale.
Discussion
The present study implemented software to assess the probability of aspiration pneumonia in patients with acute ischemic stroke. It is not noted in the literature that any software can predict aspiration pneumonia in this population.
Studies have shown that NOD with risk of tracheal aspiration is present in up to half of patients after acute ischemic stroke.9 10 25 This finding is similar to the one obtained in the present study, in which 22 (42.5%) had oropharyngeal dysphagia in clinical swallow evaluation and 18 (34.6%) in the instrumental evaluation. The difference in values between assessments is probably due to the fact that in the clinical swallow evaluation, some patients showed signs of tracheal aspiration such as coughing, wet voice, and dyspnea,23 which was not confirmed in the instrumental evaluation.
Importantly, often the clinical swallow evaluation is used to determine the next procedure with the patient in the acute phase of ischemic stroke—that is, if oral diet is or not safe for the patient.18 26 Some authors recommend a clinical swallow evaluation initially followed by an instrumental evaluation as a complementary test.26 In this study, all patients also submitted to the instrumental assessment, and the prevalence of tracheal aspiration was tested in liquid consistency. A recent study indicated that food in a liquid consistency is more likely to induce laryngeal penetration and that increased viscosity of food reduces the possibility of tracheal aspiration.27 28
After the instrumental evaluation, patients were classified by the Severity Scale20; nothing was found in the literature correlating the scale with aspiration pneumonia. Nevertheless, in our study the three patients with aspiration pneumonia scored 3, 7, and 8 in the Rosenbeck Scale,20 resulting in death, agreeing with the authors that patients with tracheal aspiration can have aspiration pneumonia leading to morbidity and mortality of patients.9 29
Our goal was to introduce clinical and instrumental swallow evaluation data in the software using the same variables present in a previous study.21 After analysis, the probability of each patient to develop aspiration pneumonia was assessed in percentages. It is noteworthy that the small number of cases of aspiration pneumonia in this study do not invalidate the variables used in the software, as they are consistent with aspiration pneumonia.
It is also important to mention that all patients, including the caregiver and the family, received speech therapy guidelines regarding posture, proper use of dental prosthesis, speed during feeding, amount of food to be chewed, preparation of bolus, food consistency, and head posture to prevent tracheal aspiration and consequently the nondevelopment of pneumonia. These positive results in our study are similar to other studies that show a reduction in clinical complications with preventive and therapeutic measures in acute stroke patients.26
Teamwork of a multidisciplinary unit with a speech therapist ensures patient safety during feeding and avoids the risks of tracheal aspiration.
Conclusion
The software is indicative of the probability of the patient having aspiration pneumonia, but the sample was not sufficient. A larger sample size is required, along with continuity of this study.