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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
Stroke. Author manuscript; available in PMC 2010 April 1.
Published in final edited form as:
PMCID: PMC2742675

Post-acute Re-evaluation may Prevent Dysphagia-Associated Morbidity


Background and Significance

Accurate identification and tailored management of patients with dysphagia is necessary to prevent complications when dysphagia is present and avoid implications of dietary restriction when unnecessary. Methods of dysphagia assessment vary, and a re-assessment in the post-acute period is not an established standard. The aim of this retrospective study was to compare initial dysphagia assessment with dysphagia re-assessment results for stroke patients admitted to our inpatient rehabilitation facility.


We examined medical records of 226 acute stroke patients admitted to our inpatient rehabilitation facility from Dec 2006 to May 2007. We excluded 86 subjects, then noted the presence or absence of dysphagia based upon documentation and prescribed diet and management strategies in the remaining 146 records.


Dysphagia was identified in 94 patients (64%) assessed at our facility. Of these patients, 11% (n=10) were not previously identified in acute care (non-negligible number, p<.0001). Agreement regarding presence or absence of dysphagia occurred in 85%. However, prescribed diet differed in 51% (n=75), with 12% (n=18) requiring diet downgrades upon admission for rehabilitation.


The necessity of dysphagia re-assessment as part of routine post-acute stroke rehabilitation care is not completely established. Our study supports the need for post-acute re-assessment as 11% of patients with dysphagia would not have been identified without re-assessment and 12% required diets more conservative than prescribed in acute care. Prospective research addressing dysphagia specific outcomes is warranted to develop efficient and high quality standards for preventing post-stroke dysphagia associated morbidity.

Keywords: Acute Care, Acute Stroke, Cerebrovascular Accident, Diagnostic Methods, Dysphagia, Organized Stroke Care, Prevention, Quality of Life, Stroke Care, Morbidity, Post-acute Care

Of the 780,000 people in the U.S. per year who suffer a stroke1, between 37 and 78% are estimated to suffer from dysphagia (swallowing disorder), depending on the type of assessment used2. Dysphagia can manifest during any of the three phases (oral, pharyngeal, and esophageal3) of swallowing. Complications of dysphagia include aspiration, which can lead to aspiration pneumonia and increase the risk of death by more than five fold5, and malnutrition, which is associated with poor outcome and slowed rate of recovery3,6,7.

Early evaluation for dysphagia has significantly decreased the incidence of aspiration pneumonia in stroke patients5, however a universal standard protocol for assessment has not been fully defined. The National Clinical Guidelines for Stroke recommend a clinical assessment by a trained specialist, such as a speech and language pathologist (SLP), who should advise an appropriate consistency of solids and fluids for safe swallow6. This clinical assessment, consisting of examination of voluntary movements of the mouth and throat as well as observation of the swallowing of solids and liquids of various consistencies, often occurs at the bedside. However, clinical or bedside assessment alone has been shown to be a poor predictor of pharyngeal dysphagia8,9,10,11,12, and reliance on these assessments without other objective radiographic studies has been said to be ‘unsupportable’13. The videoflouroscopic swallow study (VFSS) or modified barium swallow (MBS), which evaluates the oral, pharyngeal and early esophageal phases of swallowing, is a universally accepted clinical gold standard for assessment of dysphagia14,15,(though some studies have shown variable test-retest reliability16,17). Flexible/fiberoptic endoscopic examination of swallow (FEES), or FEES with added sensory testing (FEESST), may be used for dysphagia assessment at some institutions, but there is not sufficient evidence to support its use as an acceptable alternative gold standard to VFSS18.

VFSS has advantages beyond identification of aspiration, including the ability to observe the effectiveness of compensatory swallowing strategies (e.g. multiple swallows, chin tuck, etc.) as well as the visualization of swallowing pathology other than aspiration19. Furthermore, Martin-Harris et al found as many as 83% of patients with dysphagia who undergo a VFSS may have a change in at least 1 of 5 clinical variables related to the dysphagia treatment plan including: referral to specialist, swallowing therapy, compensatory swallowing strategies, mode of nutritional intake, and diet19. While errors of inappropriate dysphagia management may occur commonly with clinical swallow assessment alone15, placing post-stroke patients at risk of dysphagia-related morbidity and mortality, one may argue that obtaining a VFSS in the first days following stroke may result in excessive cost in lost time for other diagnostic evaluations to prevent recurrent events. Furthermore, some patients may not be sufficiently alert or otherwise able to cooperate meaningfully with a VFSS in the early acute period. High morbidity and mortality associated with complications of dysphagia as well as time and costs associated with VFSS steer many institutions toward using clinical assessment alone with highly conservative management of symptomatic or high-risk patients. However, restricting patients to diets of altered consistency or prohibiting oral feeding in patients for whom these restrictions are unnecessary is also undesirable. Unnatural feeding can lead to discomfort, distortion of self-image, and severe psychological distress20. If food is less palatable, the pleasure of eating may be reduced, with has been reported to diminish quality of life21. Therefore, accurate identification and tailored management of patients with dysphagia are of utmost importance, due to the need to prevent the complications of dysphagia when present as well as the need to avoid the implications of dietary restriction when such restriction is unnecessary.

Many patients transfer from an acute to post-acute hospital setting during their stroke care. Whether the transition from acute to post-acute inpatient care appropriately includes swallowing re-assessment is undefined. In some post-acute rehabilitation settings, a new decision process regarding dysphagia assessment may not be considered necessary or cost effective. However, documentation of initial dysphagia assessment is not always included in transfer records, even when a modified diet indicates suspected or diagnosed dysphagia. While consensus statements suggest ongoing monitoring and evaluation of swallowing22, specific guidelines for dysphagia re-assessment during inpatient stroke rehabilitation are not available. To manage stroke patients with possible dysphagia efficiently and safely, our institution developed a protocol for clinical re-assessment. A high percentage of these patients go on to have a VFSS. Based on a clinical impression over several years of the effectiveness of dysphagia re-assessment in identifying patients at risk of aspiration, we wished to retrospectively compare initial acute care dysphagia assessment with dysphagia re-assessment results for stroke patients admitted to our inpatient rehabilitation facility. We hypothesized that differences in dysphagia identification and management between initial and re-assessment would exceed those expected as a result of interim natural recovery, and that dysphagia re-assessment would detect dysphagia not identified on initial screening.


Our center, the Kessler Institute for Rehabilitation Saddle Brook facility (KIRSB) is a freestanding inpatient rehabilitation hospital located in Saddle Brook, NJ, which admits stroke patients immediately following the acute care hospitalization. Stroke patients participate in an interdisciplinary rehabilitation program that includes at least 3 hours of therapy a day, 6 days per week for an average of 2 to 3 weeks. Goals include maximizing recovery and functional independence, training of caregivers, and patient and family education.

We retrospectively identified patient records for this study from a list of all patients with a diagnosis of acute stroke admitted to KIRSB from Dec 2006 to May 2007, obtained from eRehab Data, an inpatient rehabilitation outcomes database sponsored by the American Medical Rehabilitation Providers Association (AMRPA). We examined hard copy charts of the first 226 patient records obtained, along with electronic medical records and acute care hospital transfer records. Each subject was de-identified and protected health information was secured according to our institutional guidelines and policies. Information collected for each subject was recorded on a separate case report file.

Twenty-one subjects were excluded when we determined there was no actual diagnosis of acute stroke (n=17) or for unavailability or the medical records (n=4). Twenty-two charts documented care for patients who were transferred back to the acute care setting and then later readmitted to KIRSB during the above stated timeframe. Subjects with readmissions to our facility were represented only once in our data analysis. Four of these subjects were found to have an additional acute stroke as their reason for transfer, and only data from their first admission was included. The remaining 18 of these subjects were transferred for reasons other than a new acute stroke (e.g. infection). Data from both KIRSB admissions was collapsed in subjects who had been transferred back to acute care early in their post-acute rehabilitation stay (within the first few days) and who completed dysphagia assessment upon return. If the transfer occurred beyond the first few days of rehabilitation, then only our initial admission dysphagia assessment was used. We could not find documentation of dysphagia re-assessment at KIRSB for thirty-seven patients who were also excluded from data analysis.

In the remaining 146 charts, we noted the presence or absence of dysphagia based upon prescribed diet upon transfer to rehabilitation, review of diagnoses listed in transfer records and progress notes when provided (see Figure 1). We considered subjects admitted with NPO status who had no other stated medical reason for such status to have been given a diagnosis of dysphagia in acute care. Also, we considered patients who had been prescribed a diet of altered consistency, such as thickened liquids or pureed food, without other stated reason for such restrictions to have been given a diagnosis of dysphagia in acute care. It should be noted that two subjects had been prescribed a diet of mechanically soft solids due to the fact that they were edentulous. We did not consider these subjects to have a diagnosis of dysphagia. Other information collected included: age at stroke onset; gender; type of stroke; length of time from onset of stroke to rehabilitation admission; type of dysphagia assessment performed in acute care; diet prescribed in acute care; dysphagia strategies and treatment prescribed in acute care; type of dysphagia assessment done at KIRSB; documented findings upon dysphagia assessment at KIRSB; diet prescribed at KIRSB; and dysphagia strategies and treatment prescribed at KIRSB.

Figure 1
Flow chart of records reviewed and included for analysis.

We examined change in diet prescription as a result of KIRSB assessment. Using a chi-square goodness-of-fit test, we compared actual change with predicted change, figures generated from estimates of the proportion of subjects who might be expected to recover, based on published literature regarding the natural history of dysphagia3.


Of 146 qualifying subjects, 46% were women and 54% were men. Age ranged from 28 to 102 years, with a mean age of 72 at the time of admission. Average length of time from onset of stroke to inpatient rehabilitation admission was 11 days. The majority (87%) of subjects suffered ischemic strokes while 11% suffered primary hemorrhages. In three cases (2%), we could not determine stroke type from the records. Table 1 summarizes these general characteristics of our sample.

Table 1
General characteristics of stroke patient sample

Documentation of initial dysphagia assessment during acute hospitalization is summarized in Table 2. In 36% of subjects, there was documentation that some type of dysphagia assessment was performed. “Clinical exam only” was documented in 10%, “VFSS only” in 13%, “clinical exam + VFSS” in 2%, “clinical exam + FEES” in 2%, and in 9% the type of assessment was not specified. In 64% of subjects, we found no documentation about dysphagia assessment in the acute care records provided upon transfer to inpatient rehabilitation. In those patients, we determined whether dysphagia had been identified in acute care based on the prescribed diet upon transfer to rehabilitation, review of diagnoses listed in transfer records, and progress notes when provided.

Table 2
Acute Care Documentation of Dysphagia Assessment

Once admitted to KIRSB, 68% of subjects (n=99) underwent a VFSS as part of our dysphagia re-assessment protocol. The remaining 32% (n= 47) had a clinical examination only to determine presence or absence of dysphagia. Table 3 summarizes dysphagia identification in acute care and KIRSB. Agreement regarding presence or absence of dysphagia occurred in 85% (124/146). Dysphagia was identified in 94 patients (64%) at KIRSB. Of these patients, 86% (n=81) were confirmed by VFSS and 11% (n=10) had not been previously identified in acute care. Twelve patients (8.2%) previously identified with dysphagia in acute care no longer had evidence of dysphagia when admitted for rehabilitation at KIRSB.

Table 3
Dysphagia Identification in acute care and at KIRSB

Table 4 highlights changes in diet upon admission to KIRSB. Agreement in prescribed diet occurred in only 49% (n=71). The KIRSB dysphagia assessment resulted in a diet upgrade in 36% (n=53) and a downgrade in 12% (n=18). Four patients (3%) had either an upgrade in solids with concomitant downgrade in liquids (or the reverse) or a change in diet that could not be classified secondary to a liquid consistency prescribed in acute care that was less specific than the categories used at KIRSB (e.g. “thickened liquids”, not otherwise specified). We predicted the proportion of patients in whom recovery would be expected based on published literature regarding the natural history of dysphagia2. The 18 patients who had diet downgrades upon admission to KRISB were in statistically significant excess over the hypothesized count of 1 patient using the exact chi-square goodness-of-fit test for one-way tables (p<.0001).

Table 4
Changes in diet upon admission to KIRSB


Dysphagia was common (64%) in this post-stroke patient sample and was present in a proportion consistent with the upper limit of published statistics for the acute stroke period2. Little has been published about the natural history of post-stroke dysphagia, and current references may underestimate its prevalence during the time period corresponding to inpatient rehabilitation. Overall characteristics of our sample seem to be representative of the general population of patients with stroke entering the post-acute rehabilitation setting. Further research may be needed to ensure that the need for care of stroke survivors with dysphagia is appropriately estimated.

Based on the clinical assumption of the necessity for dysphagia re-assessment at our center and others, and the lack of empiric objective data to support this assumption, we wished to examine a body of existing data to see if re-assessment in the post-acute period is indeed important in stroke care. We chose to employ a retrospective design to accomplish this aim, despite the fact that several confounds affect the objectivity of the medical record. Retrospective design is limited by the quality and completeness of the medical record data available, and therefore we did not expect this information to determine utility of dysphagia re-assessment conclusively. Additionally, variability in timing between initial and re-assessments, inability to employ a standardized tool for dysphagia assessments, and biases resulting from the fact the post-acute evaluators were not blinded to acute care assessment results may also potentially limit the validity of the study conclusions.

Documentation of initial acute care dysphagia assessment is not reliably included in transfer records for inpatient rehabilitation hospitals. In our study, transfer records for the majority of subjects (64%) did not include documentation of acute care dysphagia assessment. Adequate description of the dysphagia care plan is needed during transitions from acute settings to provide the highest quality care, especially since specific guidelines for dysphagia assessment during stroke rehabilitation do not exist, and re-assessment of stroke patients may not be considered necessary or cost-effective in some post-acute rehabilitation settings. At KIRSB, the majority of stroke patients are re-assessed via clinical examination, a high percentage of which are confirmed via VFSS. If patient assessment during acute care were sufficient to identify dysphagia, then we should see differences between results of acute and KIRSB assessments only if accounted for by natural recovery. Likewise, prescribed diet at KIRSB should be either the same as that prescribed in acute care or upgraded if recovery has taken place. We refer to these differences as ‘disagreement,’ recognizing that agreement between acute and post-acute assessments is not expected since dysphagia status is expected to change over time. However, new identification of dysphagia or downgrading of prescribed diet on admission to acute rehabilitation may reflect a failure to adequately detect dysphagia in the acute care setting. While it is possible that patients who suffer from mild strokes that evolve over time may not show signs of dysphagia in the acute period, this only further supports re-assessment in the post-acute phase. In our study, 11% of patients with dysphagia would not have been identified without reassessment. This suggests that both initial assessment and later re-assessment may be necessary for optimal care for dysphagia.

Agreement in prescribed diet between acute care and rehabilitation occurred in only 49%, suggesting a great need to repeat dysphagia assessments in the rehabilitation setting. A disturbing number of patients (12%, n=18) required diets for swallowing safety more conservative than those prescribed in acute care. This proportion of diet downgrades upon admission to KIRSB was a statistically significant excess over the <1% hypothesized using the exact chi-square goodness-of-fit test for one-way tables (p<.0001). Using published literature regarding the natural history of dysphagia3, we predicted the proportion of patients who would be expected to show recovery (36%). As predicted, diet levels were upgraded upon admission for rehabilitation in 36%. This proportion of diet upgrades likely represents changes due to interim natural recovery, though overly conservative management in acute care, perhaps due to inability of patients to cooperate with advanced diagnostic procedures, is also a possible explanation. Whether this trend represents recovery or overly conservative management is a question requiring prospective examination so that unnecessary dietary restriction can be avoided, especially since implications of such restriction can include malnutrition, discomfort, distortion of self-image, psychological distress, reduced pleasure of eating and diminished quality of life3,20,21.


A high percentage of stroke patients entering the post-acute setting suffer from dysphagia, which is associated with great morbidity. A considerable proportion of these patients may not have been diagnosed during the acute hospitalization. Patients diagnosed with dysphagia in the acute period who have recovered substantially by the post-acute period may be receiving unnecessary dietary restrictions, which also contribute to morbidity. The currently recommended process of swallow assessment is not standardized, and a complete swallow evaluation may appropriately include both initial and re-assessment stages. Acute care clinicians should outline the request for dysphagia re-assessment along with any other follow up instructions to be included upon transfer to post-acute settings as part of quality continuity of post-stroke care. Clinicians treating stroke patients in post-acute inpatient settings should not consider results of prior dysphagia assessment to be conclusive. Our results support the need for re-assessment upon admission for post-acute inpatient rehabilitation. We recommend prospective investigation of an assessment/re-assessment protocol, which would include an initial acute assessment occurring within the first 14 days followed by a post-acute re-assessment conducted between weeks 2–8. Future research qualifying dysphagia severity and characteristics, severity of subjects’ neurologic deficits, and addressing dysphagia specific outcomes will be necessary to develop efficient and high quality standards for preventing post-stroke dysphagia associated morbidity.

Supplementary Material


1. This research was conducted in conjunction with the Stroke Rehabilitation Fellowship program sponsored by the University of Medicine and Dentistry of New Jersey, the Kessler Medical Rehabilitation Research and Education Center, and the Henry H. Kessler Foundation. The above institutions sponsor the Stoke Rehabilitation Fellow, Kimberly Heckert, who conducted the research without additional specific funding sources. The work was also supported by the National Institutes of Health, National Institute of Neurological Disorders and Stroke (K02NS97099, Barrett).

2. The authors are grateful for the helpful suggestions for improvement of this manuscript provided by 3 anonymous reviewers, one of whom suggested we specifically recommend a standardized protocol for dysphagia assessment in the acute and post-acute phases to be tested in future prospective investigation. The authors wish to acknowledge Dr. Bruce Pomeranz for assistance with administrative resources, Michael Slifer and Joan Alverzo for critically assisting with identification of records for review, the Medical Records Staff at Kessler Institute for Rehabilitation Saddle Brook Facility for assistance with record retrieval, and Marita Delmonico and Eileen Kirk for assistance with information resources.

Contributor Information

Kimberly D. Heckert, Kessler Medical Rehabilitation Research and Education Center, University of Medicine and Dentistry of New Jersey.

Eugene Komaroff, Director, Biostatistics and Clinical Trials, Kessler Medical Rehabilitation Research and Education Center, Associate Professor of Physical Medicine & Rehabilitation, University of Medicine and Dentistry of New Jersey, New Jersey Medical School.

Uri Adler, Assistant Professor of Physical of Medicine and Rehabilitation, University of Medicine and Dentistry of New Jersey, New Jersey Medical School, Director, Stroke Services, Kessler Medical Rehabilitation Research and Education Center.

Anna M. Barrett, Associate Professor, Physical Medicine and Rehabilitation, Neurology and Neurosciences, University of Medicine and Dentistry of New Jersey, New Jersey Medical School, Director, Stroke Rehabilitation Research, Kessler Medical Rehabilitation Research and Education Center.


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