Abstract
Background
Aspiration pneumonia is an important cause of morbidity and mortality in Parkinson’s disease (PD). Clinical characteristics of PD patients in addition to specific alterations in swallowing mechanisms contribute to higher swallowing times and impairment in the effective clearance of the airway. These issues may render patients more prone to dysphagia and aspiration events. We aimed to determine the frequency of aspiration events in a hospitalized PD cohort, and to report the number of in-hospital swallow evaluations.
Methods
A retrospective single center chart review of 212 PD patients who had 339 hospital encounters was performed from January 2011 to March 2013. Demographics, clinical characteristics, and reasons for encounters were documented. The number of in-hospital aspiration events and the number of swallowing evaluations and also the implementation of aspiration precautions were recorded.
Results
The cohort had a mean age of 74.1 (SD = 10.1) years with mean disease duration of 6 (SD = 6.3) years. Fifty-two hospital encounters (15.3 %) were related to a pulmonary cause. In-hospital aspiration pneumonia events were reported in 8 (2.4 %) of the total encounters. Swallow evaluations were performed in 25 % of all cases, and aspiration precautions were initiated in 32 % of the encounters. The data revealed that 1/8 patient had swallowing evaluations performed prior to an aspiration event.
Conclusions
In-hospital aspiration pneumonia events were reported in 2.4 % of the hospitalized PD cohort. Preventive measures and precautions were not routinely performed, however rates of aspiration were relatively low. The results highlight the need for more research into screening and monitoring of swallowing problems in PD patients during hospital encounters.
Keywords: Hospitalization, Pneumonia, Dysphagia, Swallow therapy, Prevention
Background
Parkinson’s disease (PD) is a neurodegenerative disorder characterized by the presence of cardinal motor symptoms such as bradykinesia, tremor, rigidity, and loss of postural reflexes [1]. Over the last few decades, there has been an expanded concept recognizing numerous non-motor characteristics of PD beyond the usual motor symptoms, including neuropsychiatric disorders, sleep disturbances, autonomic, sensory, and gastrointestinal symptoms [2]. These non-motor symptoms become more prevalent as the disease advances and have been cited as a major cause of disability. The recognition of these symptoms will likely be critical for improving healthcare for the expanding PD population [3, 4].
Dysphagia in PD has been shown to be associated with aspiration pneumonia, which is one of the potential reasons for PD hospitalization [5, 6]. Swallowing is a sensorimotor process involving automatic and volitional systems, where decreased cough sensitivity and elevation and excursion of the hyolaryngeal complex have been considered important causes of penetration and aspiration in PD patients [7, 8]. PD patients experience higher rates of hospital-based complications, and often suffer substantial clinical deterioration while hospitalized [9, 10]. It has been estimated that PD patients have a 3.8 times increased risk of developing aspiration pneumonia when compared to the general population [11]. Aspiration pneumonia has been reported as the most frequent cause of death in PD patients, and it has been estimated to account for 70 % of the mortality [12]. The recognition of potentially preventable risk factors and interventions to reduce morbidity, mortality, and economic burdens are important and relevant to this population. We aimed to evaluate the frequency of aspiration events in patients with PD during hospital encounters, and we documented the care practices for these patients.
Methods
The University of Florida (UF) Institutional Review Board (IRB) reviewed and approved the study. Patient records were de-identified prior to analysis.
Study design, settings, and population
A dataset of 339 hospital encounters from 212 patients followed at the UF Center for Movement Disorders and Neurorestoration (CMDNR) was used. The dataset included the period from January 2011 to March 2013 and the study was conducted as a retrospective cross-sectional data/chart review. A diagnosis code (International Classification of Diseases, Ninth Revision, Clinical Modification) was used to identify subjects with PD (ICD-9-CM code 332.0) who had a hospital encounter and this was used as criteria for inclusion into the study. A hospital encounter was defined as an emergency room visit with subsequent hospitalization, or any direct admission to the hospital due to any cause with the exception of admission for elective procedures.
Data collection
An electronic health record system (EPIC) was used to obtain the basic demographics and clinical data elements from each subject’s chart at the time of the hospital encounter, including results from swallow evaluations and if aspiration precautions were administered. Additionally, the reason for hospital encounter, length of hospital stay in days, and whether a neurologist was consulted during these encounters were also documented. LED was calculated using the following formula [13]: regular LD dose + LD CR dose × 0.75 + LD × 0.33 if entacapone + pramipexole dose × 100 + ropinirole dose × 20 + rotigotine dose × 30 + pergolide dose × 1 + bromocriptine dose × 10 + selegiline dose × 10 + rasagiline dose × 100 + amantadine dose × 1. The Charlson index score, which has previously been used in studies with PD patients [14] was chosen to evaluate the magnitude of impact of each of the comorbidities on the mortality risk [15]. The Charlson index predicts the ten-year mortality for each patient based on comorbidities. Each condition is assigned a score of 1, 2, 3, or 6, depending on the risk of dying associated with each one. Scores are summed to provide a total score to predict mortality. Conditions screened by the Charlson index are cardiovascular disorders, pulmonary diseases, cerebrovascular diseases, connective tissue diseases, liver and kidney diseases, diabetes, dementia, cancer, and/or AIDS. We further divided patients into subgroups including those with or without alteration in mental status according to the physicians clinical examination note at the time of evaluation. Reasons for hospital encounters were categorized based on the Emergency Severity Index (ESI) triage algorithm [16] which classifieds the documented reasons for hospitalization. According to this algorithm, an ESI 1 and 2 were classified as a high risk for a prolonged length of stay, including falls/fractures, pulmonary causes (such as chronic obstructive pulmonary disease, cancer, pulmonary arterial hypertension, fibrosis, vascular disease, pneumonia), cardiac issues/syncope, genitourinary infections, encephalopathy/drug-induced psychosis, cancer, stroke, and dementia, and an ESI 3–5 was classified as low risk, and was inclusive of general medical conditions (including weakness, pain, bleeding, or anorexia), other medical issues (including seizures, vascular problems, or trauma), and gastrointestinal issues.
Outcome measurements
The primary outcome was the frequency of aspiration pneumonia in a cohort of PD patients during their hospital encounter. Also collected were the circumstances for the aspiration event, including clinical features of the individual and environmental features such as the occurrence of swallow evaluations and aspiration precautions.
To identify subjects who developed aspiration pneumonia during the encounter (in-hospital aspiration) we used a diagnosis code (ICD-9-CM code 507.0, 507.8, and 997.32) and performed a manual chart review of each subject and each hospital encounter in order to identify aspiration pneumonia events that occurred at 48 h or greater after the hospital encounter. The frequency of aspiration pneumonia was calculated by dividing the number of hospital-acquired aspiration pneumonias by the total number of hospital encounters, and this was then multiplied by 100. A brief description of the swallowing evaluations and aspiration precautions is provided in following paragraphs.
Clinical or bedside swallow evaluation (CSE)
The CSE was performed for all patients referred for a swallow evaluation. The assessment included: 1. Patient awake/oriented/able to follow simple commands, 2. Ability to produce sustained phonation and comment on vocal quality, 3. Ability to produce voluntary cough on command, 4. Ability to produce saliva, swallow on command, and observation of hyolaryngeal elevation, 5. Trials of ice-chips: observation of oral bolus manipulation; chew (if present); timeliness of pharyngeal swallow; hyolaryngeal elevation; cough after swallow; voice quality after swallow, and 6. Trials of thin, nectar-thick, honey-thick liquids as deemed appropriate by the speech-language pathologist (SLP): Anterior labial leakage, timeliness of pharyngeal swallow, hyolaryngeal elevation, cough after swallow, and voice quality after swallow.
Rehabilitation barium swallow evaluation (RBS)
The decision to perform a RBS was made following a CSE and if the patient exhibited signs or symptoms of an impaired swallowing mechanism. These signs included one or more of the following: weak or absent volitional cough, cough after swallow, voice change after swallow, absent volitional swallow, reduced or delayed hyolaryngeal elevation. The RBS was performed in the fluoroscopy suite of the radiology department. Patients were seated upright in the lateral viewing plane, and multiple boluses of thin, thick, and solid consistencies were presented for evaluation by the SLP.
Aspiration precautions
The recommendation for aspiration precautions was potentially performed before or possibly after the swallow evaluations (whether CSE or RBS). These were typically administered pre-emptively to patients considered by the nurses or physicians to be at-risk for aspiration, but they could also be administered after a swallowing study. The recommendations ranged from nothing by mouth (NPO) in extreme cases of disordered swallowing, or included modifications such as supervision during eating/drinking, sitting upright in a chair, thickened liquids, crushed pills, IV administered pills/medications, or various “dysphagia diets” (i.e., mechanical soft, puree, etc.).
Statistical analysis
A Mann–Whitney U Test was used to compare demographics and continuous variables (age, Charlson index, disease duration, levodopa equivalent dosage, days from admission to swallow evaluations and aspiration precautions, and length of hospital encounter) between those who developed aspiration pneumonia versus those who did not develop aspiration pneumonia. A Chi square test using an Exact Test was performed to compare categorical variables (gender, H&Y stage, and neurology consultation) between populations and to learn whether preventive swallowing measures had an effect on developing aspiration pneumonia during the hospital encounter. Statistical analyses were performed using commercially available statistical software (SPSS, version 19.0; SPSS, Inc., Chicago, Illinois) with a priori alpha levels of ≤ 0.05.
Results
Characteristics of population
Sixty-one percent were male, with a mean age of 74.1 (SD = 10.1) years, and a mean Charlson index of 5.9 (SD = 1.5). The cohort had mean disease duration of 6.4 (SD = 6.3) years and had mean LED of 502.4 (SD = 487.9) mg. A neurologist was consulted in 24.5 % and the mean length of hospital stay was of 6 (SD = 7.1) days. No demographic and clinical significant differences were found when comparing those who developed aspiration pneumonia during hospital encounter versus those who did not develop aspiration pneumonia, as shown in Table 1. A pulmonary reason was the cause leading to a hospital encounter in 52/339 (15.3 %). The reasons for hospital encounters have been described in Table 2.
Table 1.
Demographic and clinical comparison between populations
| Total (n = 339) | Aspiration pneumonia (n = 8) | Non-aspiration pneumonia (n = 331) | P | |
|---|---|---|---|---|
| Age, y (SD) | 74.1 (10.1) | 76.6 (12.4) | 74.1 (10.1) | 0.62a |
| Male, no. (%) | 206 (60.8 %) | 4 (50) | 202 (61) | 0.72b |
| Charlson index, no. (SD) | 5.9 (1.5) | 5.9 (1.1) | 5.9 (1.5) | 0.90a |
| Disease duration, y (SD) | 6.4 (6.3) | 3.8 (2.2) | 6.4 (6.3) | 0.59a |
| Hoehn and Yahr stage IV-V, no. (%) | 165 (48.7) | 4 (50) | 161 (48.6) | 1.00b |
| LED, no. (SD) | 502.4 (487.9) | 716.6 (488.5) | 496.8 (487.5) | 0.15a |
| Neurologist consulted, no. (%) | 83 (24.5) | 1 (12.5) | 82 (24.8) | 0.71b |
| Length of hospital stay, days (SD) | 6 (7.1) | 4.3 (3.6) | 6.0 (7.2) | 0.56a |
| Swallow evaluations or aspiration precautions, no. (%) | 158 (46.6) | 7 (87.5) | 1 (12.5) | 0.03b |
| Days from admission to barium evaluation, no. (SD) | 4.5 (4.3) | 4.3 (4.3) | 4.5 (4.4) | 0.98a |
| Days from admission to clinical evaluation, no. (SD) | 3.5 (4.7) | 4.3 (2.2) | 3.5 (4.8) | 0.13a |
aMann–Whitney U Test
bFisher’s Exact Test
Table 2.
Reasons for hospital encounters (n = 339)
| Frequency | Percentage | |
|---|---|---|
| Falls/fractures | 61 | 18 |
| Pulmonary | 52 | 15.3 |
| General medical problems | 51 | 15 |
| Other | 48 | 14.2 |
| Gastrointestinal issues | 43 | 12.7 |
| Encephalopathy/drug-induced psychosis | 24 | 7.1 |
| Cardiac issues/syncope | 22 | 6.5 |
| Stroke | 19 | 5.6 |
| Genitourinary infections | 13 | 3.8 |
| Cancer | 6 | 1.8 |
Aspiration pneumonia, swallow evaluations and aspiration precautions
Aspiration pneumonia events were reported in 8 (2.4 %) hospital encounters of 8 individual patients. The reasons for hospital encounters were: 3 due to general medical problems, 2 due falls/fractures, 2 due to other pulmonary causes, and 1 due to other reasons. Seven subjects of the 8 who developed aspiration pneumonia during the hospital encounter were considered as having a high-risk reason of admission, X2 (2) = 2.9, p = 0.09. Two of the 8 subjects had altered mental status at admission and there was no significant difference in the frequency of aspiration events when compared to those without alteration, X2 (2) = 0.36, p = 0.72. Additionally, 6/52 (11.5 %) hospital encounters that were related to pulmonary causes were due to an aspiration pneumonia acquired outside the hospital.
The swallow evaluations were performed in 83/339 (24.5 %) while aspiration precautions were adopted in 116/339 (34.2 %) of the hospital encounters. The mean days from admission until swallow evaluation was of 4.5 (SD = 4.3) for RBS and 3.5 (SD = 4.7) for CSE. A greater percentage of swallow evaluations and aspiration precautions was performed on those who developed in-hospital aspiration pneumonia, 7/8 (87.5 %) vs. 1/8 (12.5 %), X2 (2) = 5.51, p < 0.03. The evaluations and/or precautions were implemented after the occurrence of aspiration pneumonia in 7/8 cases. Two of the 8 in-hospital aspiration pneumonia events developed after an intubation procedure.
Discussion
This retrospective cross-sectional review of 339 hospital encounters revealed a frequency of in-hospital aspiration pneumonia of 2.4 %. Studies have reported an estimated incidence of community-acquired pneumonia in PD patients varying between 11–60 % [17, 18], but there has been a lack of data on hospitalized patients.
This cohort demonstrated a surprisingly low frequency of in-hospital swallowing evaluations and also there was a low amount of education offer in hospital for aspiration precautions. Swallowing evaluations were ordered in less than 25 % of cases, and there was a mean delay from admission of 3–5 days. Aspiration precautions were administered in less than 35 % of the hospital encounters. Swallow evaluations were more frequently implemented following the discovery of hospital-acquired aspiration pneumonia. A closer inspection of the data revealed that two of the eight in-hospital aspiration pneumonia events developed after an intubation procedure.
The original reports of swallowing complications in PD were published in the 1980s [19], and since that time there has been a recent interest in aspiration in this population, and this interest has been magnified by the published associations of aspiration with morbidity and mortality. PD patients without symptoms of dysphagia have prolonged swallowing times [20, 21] and impairments in the ability to effectively clear the airways [7, 22, 23]. These attributes render these patients more prone to developing dysphagia and to subsequent aspiration. Recent studies have also detected microscopic neural degeneration, regenerative changes [24], and deposition of alpha-synuclein in the pharyngeal structures [25], and these could possibly be the pathophysiological underpinnings of swallowing abnormalities in PD.
Interestingly, the demographic, clinical characteristics, or mental status at admission correlated with aspiration events. However, we did observe a tendency for developing aspiration pneumonia in high-risk patients with prolonged length of stay. In the future it will be important to detect high-risk PD patients for aspiration at the time of the hospital admission. Awareness among hospital staff and physicians and the implementation of preventative measures could be a critical change in practice. Whether addressing these issues could decrease the incidence of aspiration remains unknown.
Preventative measures have been proposed as fundamental for decreasing aspiration-related morbidity and mortality in PD [26, 27]. Swallowing function usually does not respond to levodopa therapy, however in some cases it may be partially improved [28], non-pharmacological measures [29] such as providing adequate nutrition without sacrificing airway safety are also important. There are no standardized guidelines for the management of the hospitalized PD patients and better management protocols are needed [30, 31].
There were several limitations of this study. The retrospective nature of the data obtained from ER clinical notes could have possibly resulted in missing aspiration cases and inaccurate staging of the disease. Additionally, the cognitive profile was not well documented for all patients. Second, we based the diagnosis of aspiration pneumonia on the physician’s clinical note. The use of microbiological cultures from pulmonary aspirates could have possibly improved diagnostic certainty. Third, the data was culled from a referral center of movement disorders and all patients were followed in an expert PD clinic, which routinely performs swallow evaluations, and this may have biased the low rate of aspiration events. Finally, the use of non-validated stratifying indexes (in PD populations) may have limited the validity of the data. The assessment of length of hospital stay was based on the Charlson index, which consider various comorbidities. We were not able to control for these comorbidities including dementia [32] and to control for stroke or diabetes [33]. These comorbidities can impact risk of aspiration. The comorbidity issue could not be completely addressed due to a lack of statistical power for such an analysis. Finally, the population had a mean disease duration of 6 years, which could have possibly underestimated the incidence, and magnitude of the results.
Conclusions
In summary, though in-hospital aspiration pneumonia events were reported to be low in our PD cohort this should not diminish the importance of these events. Swallowing evaluations and precautions were routinely underutilized. Additional larger prospective studies from a community hospital sample will be necessary to better understand risk factors, preventative strategies, and also longitudinal follow-up of in-hospital aspiration events.
Acknowledgments
We would like to acknowledge the support of the National Parkinson Foundation, Tyler’s Hope and the Bachmann-Strauss Foundation. Also we would like to acknowledge the UF Foundation and the UF INFORM database.
Footnotes
Daniel Martinez-Ramirez and Michael S. Okun contributed equally to this work.
Competing interests
No financial disclosure or conflict of interest concerning the research related to the manuscript. No potential conflicts of interest in the last 5 years for each of the following authors (initials): DMR, LA, JCG, BA, MH, CSL, JPC, CM, AWS, CWH, KWH. MSO serves as a consultant for the National Parkinson Foundation, and has received research grants from NIH, NPF, the Michael J. Fox Foundation, the Parkinson Alliance, Smallwood Foundation, the Bachmann-Strauss Foundation, the Tourette Syndrome Association, and the UF Foundation. Dr. Okun has previously received honoraria, but in the past >48 months has received no support from industry. Dr. Okun has received royalties for publications with Demos, Manson, Amazon, Smashwords, and Cambridge (movement disorders books). Dr. Okun is an associate editor for New England Journal of Medicine Journal Watch Neurology. Dr. Okun has participated in CME activities on movement disorders (in the last 36) months sponsored by PeerView, Prime, and by Vanderbilt University. The institution and not Dr. Okun receives grants from Medtronic and ANS/St. Jude, and the PI has no financial interest in these grants. Dr. Okun has participated as a site PI and/or co-I for several NIH, foundation, and industry sponsored trials over the years but has not received honoraria.
Authors’ contributions
DMR made contributions to conception and design, acquired, analyzed, and interpreted data, drafted the manuscript, gave final approval of the version to be published, and agreed to be accountable for all aspects of the work. LA acquired and interpreted data, drafted the manuscript, gave final approval of the version to be published, and agreed to be accountable for all aspects of the work. JCG acquired and interpreted data, drafted the manuscript, gave final approval of the version to be published, and agreed to be accountable for all aspects of the work. BA acquired and interpreted data, drafted the manuscript, gave final approval of the version to be published, and agreed to be accountable for all aspects of the work. MH acquired and interpreted data, drafted the manuscript, gave final approval of the version to be published, and agreed to be accountable for all aspects of the work. CSL acquired and interpreted data, drafted the manuscript, gave final approval of the version to be published, and agreed to be accountable for all aspects of the work. JPC acquired and interpreted data, drafted the manuscript, gave final approval of the version to be published, and agreed to be accountable for all aspects of the work. CM acquired and interpreted data, drafted the manuscript, gave final approval of the version to be published, and agreed to be accountable for all aspects of the work. AWS interpreted data, drafted the manuscript, gave final approval of the version to be published, and agreed to be accountable for all aspects of the work. CWH interpreted data, drafted the manuscript, gave final approval of the version to be published, and agreed to be accountable for all aspects of the work. KWH acquired and interpreted data, drafted the manuscript, gave final approval of the version to be published, and agreed to be accountable for all aspects of the work. MSO made contributions to conception and design, analyzed and interpreted data, drafted the manuscript, gave final approval of the version to be published, and agreed to be accountable for all aspects of the work.
Author’s information
DMR, LA, JCG, MH, AWS, CWH, and MSO are movement disorders trained physicians working at the UF Center for Movement Disorders and Neurorestoration. KWH is a postdoctoral graduate from the UF with research interest in speech and swallow of PD patients. BA is a physician currently working at our Center. CSL, JPC, and CM are medical students who did a research summer in movement disorders at our Center.
Contributor Information
Daniel Martinez-Ramirez, Email: Daniel.Martinez-Ramirez@neurology.ufl.edu.
Leonardo Almeida, Email: l.almeida@ufl.edu.
Juan C. Giugni, Email: juancgiugni@gmail.com
Bilal Ahmed, Email: Bilal.Ahmed@neurology.ufl.edu.
Masa-aki Higuchi, Email: masa.higuchi.29@gmail.com.
Christopher S. Little, Email: chris08@ulf.edu
John P. Chapman, Email: parkerchap@ufl.edu
Caroline Mignacca, Email: cmignacca@ufl.edu.
Aparna Wagle Shukla, Email: aparna.shukla@neurology.ufl.edu.
Christopher W. Hess, Email: christopher.hess@neurology.ufl.edu
Karen Wheeler Hegland, Email: kwheeler@ufl.edu.
Michael S. Okun, Email: okun@neurology.ufl.edu
References
- 1.Lees AJ, Hardy J, Revesz T. Parkinson's disease. Lancet. 2009;373(9680):2055–66. doi: 10.1016/S0140-6736(09)60492-X. [DOI] [PubMed] [Google Scholar]
- 2.Chaudhuri KR, Schapira AH. Non-motor symptoms of Parkinson's disease: dopaminergic pathophysiology and treatment. Lancet Neurol. 2009;8(5):464–74. doi:10.1016/S1474-4422(09)70068-7. [DOI] [PubMed]
- 3.Martinez-Martin P, Schapira AH, Stocchi F, Sethi K, Odin P, MacPhee G, et al. Prevalence of nonmotor symptoms in Parkinson's disease in an international setting; study using nonmotor symptoms questionnaire in 545 patients. Mov Disord. 2007;22(11):1623–9. doi: 10.1002/mds.21586. [DOI] [PubMed] [Google Scholar]
- 4.Seppi K, Weintraub D, Coelho M, Perez-Lloret S, Fox SH, Katzenschlager R, et al. The Movement Disorder Society Evidence-Based Medicine Review Update: Treatments for the non-motor symptoms of Parkinson's disease. Mov Disord. 2011;26(Suppl 3):S42–80. doi: 10.1002/mds.23884. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Fernandez HH, Lapane KL. Predictors of mortality among nursing home residents with a diagnosis of Parkinson's disease. Med Sci Monit. 2002;8(4):CR241–6. [PubMed] [Google Scholar]
- 6.Torres A, Peetermans WE, Viegi G, Blasi F. Risk factors for community-acquired pneumonia in adults in Europe: a literature review. Thorax. 2013;68(11):1057–65. doi: 10.1136/thoraxjnl-2013-204282. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Troche MS, Brandimore AE, Okun MS, Davenport PW, Hegland KW. Decreased cough sensitivity and aspiration in Parkinson disease. Chest. 2014;146(5):1294–9. doi: 10.1378/chest.14-0066. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Troche MS, Okun MS, Rosenbek JC, Musson N, Fernandez HH, Rodriguez R, et al. Aspiration and swallowing in Parkinson disease and rehabilitation with EMST: a randomized trial. Neurology. 2010;75(21):1912–9. doi: 10.1212/WNL.0b013e3181fef115. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Gerlach OH, Winogrodzka A, Weber WE. Clinical problems in the hospitalized Parkinson's disease patient: systematic review. Mov Disord. 2011;26(2):197–208. doi: 10.1002/mds.23449. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Gerlach OH, Broen MP, van Domburg PH, Vermeij AJ, Weber WE. Deterioration of Parkinson's disease during hospitalization: survey of 684 patients. BMC Neurol. 2012;12:13. doi: 10.1186/1471-2377-12-13. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Pepper PV, Goldstein MK. Postoperative complications in Parkinson's disease. J Am Geriatr Soc. 1999;47(8):967–72. doi: 10.1111/j.1532-5415.1999.tb01292.x. [DOI] [PubMed] [Google Scholar]
- 12.Mehanna R, Jankovic J. Respiratory problems in neurologic movement disorders. Parkinsonism Relat Disord. 2010;16(10):628–38. doi: 10.1016/j.parkreldis.2010.07.004. [DOI] [PubMed] [Google Scholar]
- 13.Tomlinson CL, Stowe R, Patel S, Rick C, Gray R, Clarke CE. Systematic review of levodopa dose equivalency reporting in Parkinson's disease. Mov Disord. 2010;25(15):2649–53. doi: 10.1002/mds.23429. [DOI] [PubMed] [Google Scholar]
- 14.Driver JA, Kurth T, Buring JE, Gaziano JM, Logroscino G. Parkinson disease and risk of mortality: a prospective comorbidity-matched cohort study. Neurology. 2008;70(16 Pt 2):1423–30. doi: 10.1212/01.wnl.0000310414.85144.ee. [DOI] [PubMed] [Google Scholar]
- 15.Charlson ME, Pompei P, Ales KL, MacKenzie CR. A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis. 1987;40(5):373–83. doi: 10.1016/0021-9681(87)90171-8. [DOI] [PubMed] [Google Scholar]
- 16.Gilboy N, United States . Agency for Healthcare Research and Quality. Emergency severity index. Version 4 implementation handbook. 2012 ed. AHRQ publication no. 12–0014. Rockville, MD: Agency for Healthcare Research and Quality; 2012. [Google Scholar]
- 17.Robbins J, Gensler G, Hind J, Logemann JA, Lindblad AS, Brandt D, et al. Comparison of 2 interventions for liquid aspiration on pneumonia incidence: a randomized trial. Ann Intern Med. 2008;148(7):509–18. doi: 10.7326/0003-4819-148-7-200804010-00007. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Leibson CL, Maraganore DM, Bower JH, Ransom JE, O'Brien PC, Rocca WA. Comorbid conditions associated with Parkinson's disease: a population-based study. Mov Disord. 2006;21(4):446–55. doi: 10.1002/mds.20685. [DOI] [PubMed] [Google Scholar]
- 19.Cooper RG, Carroll N, Belchetz PE. Aspiration of oral contents in Parkinson's disease. A case report. S Afr Med J. 1985;68(5):344–5. [PubMed] [Google Scholar]
- 20.Bird MR, Woodward MC, Gibson EM, Phyland DJ, Fonda D. Asymptomatic swallowing disorders in elderly patients with Parkinson's disease: a description of findings on clinical examination and videofluoroscopy in sixteen patients. Age Ageing. 1994;23(3):251–4. doi: 10.1093/ageing/23.3.251. [DOI] [PubMed] [Google Scholar]
- 21.Lin CW, Chang YC, Chen WS, Chang K, Chang HY, Wang TG. Prolonged swallowing time in dysphagic Parkinsonism patients with aspiration pneumonia. Arch Phys Med Rehabil. 2012;93(11):2080–4. doi: 10.1016/j.apmr.2012.07.010. [DOI] [PubMed] [Google Scholar]
- 22.Hegland KW, Okun MS, Troche MS. Sequential voluntary cough and aspiration or aspiration risk in Parkinson's disease. Lung. 2014;192(4):601–8. doi: 10.1007/s00408-014-9584-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Ebihara S, Saito H, Kanda A, Nakajoh M, Takahashi H, Arai H, et al. Impaired efficacy of cough in patients with Parkinson disease. Chest. 2003;124(3):1009–15. doi: 10.1378/chest.124.3.1009. [DOI] [PubMed] [Google Scholar]
- 24.Mu L, Sobotka S, Chen J, Su H, Sanders I, Adler CH, et al. Altered pharyngeal muscles in Parkinson disease. J Neuropathol Exp Neurol. 2012;71(6):520–30. doi: 10.1097/NEN.0b013e318258381b. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Mu L, Sobotka S, Chen J, Su H, Sanders I, Adler CH, et al. Alpha-synuclein pathology and axonal degeneration of the peripheral motor nerves innervating pharyngeal muscles in Parkinson disease. J Neuropathol Exp Neurol. 2013;72(2):119–29. doi: 10.1097/NEN.0b013e3182801cde. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Logemann JA, Gensler G, Robbins J, Lindblad AS, Brandt D, Hind JA, et al. A randomized study of three interventions for aspiration of thin liquids in patients with dementia or Parkinson's disease. J Speech Lang Hear Res. 2008;51(1):173–83. doi: 10.1044/1092-4388(2008/013). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Pitts T, Troche M, Mann G, Rosenbek J, Okun MS, Sapienza C. Using voluntary cough to detect penetration and aspiration during oropharyngeal swallowing in patients with Parkinson disease. Chest. 2010;138(6):1426–31. doi: 10.1378/chest.10-0342. [DOI] [PubMed] [Google Scholar]
- 28.Sutton JP. Dysphagia in Parkinson's disease is responsive to levodopa. Parkinsonism Relat Disord. 2013;19(3):282–4. doi: 10.1016/j.parkreldis.2012.11.007. [DOI] [PubMed] [Google Scholar]
- 29.van Hooren MR, Baijens LW, Voskuilen S, Oosterloo M, Kremer B. Treatment effects for dysphagia in Parkinson's disease: a systematic review. Parkinsonism Relat Disord. 2014;20(8):800–7. doi: 10.1016/j.parkreldis.2014.03.026. [DOI] [PubMed] [Google Scholar]
- 30.Gerlach OH, Rouvroije VJ, Weber WE. Parkinson's disease and hospitalization: the need for guidelines. Parkinsonism Relat Disord. 2011;17(6):498. doi: 10.1016/j.parkreldis.2011.04.004. [DOI] [PubMed] [Google Scholar]
- 31.Aminoff MJ, Christine CW, Friedman JH, Chou KL, Lyons KE, Pahwa R, et al. Management of the hospitalized patient with Parkinson's disease: current state of the field and need for guidelines. Parkinsonism Relat Disord. 2011;17(3):139–45. doi: 10.1016/j.parkreldis.2010.11.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Cereda E, Cilia R, Klersy C, Canesi M, Zecchinelli AL, Mariani CB, et al. Swallowing disturbances in Parkinson's disease: a multivariate analysis of contributing factors. Parkinsonism Relat Disord. 2014;20(12):1382–7. doi: 10.1016/j.parkreldis.2014.09.031. [DOI] [PubMed] [Google Scholar]
- 33.Hamidon BB, Nabil I, Raymond AA. Risk factors and outcome of dysphagia after an acute ischaemic stroke. Med J Malaysia. 2006;61(5):553–7. [PubMed] [Google Scholar]