National Institutes of Health Stroke Scale explained

The National Institutes of Health Stroke Scale, or NIH Stroke Scale (NIHSS), is a tool used by healthcare providers to objectively quantify the impairment caused by a stroke and aid planning post-acute care disposition, though was intended to assess differences in interventions in clinical trials. The NIHSS was designed for the National Institute of Neurological Disorders and Stroke (NINDS) Recombinant Tissue Plasminogen Activator (rt-PA) for Acute Stroke Trial and was first published by neurologist Dr. Patrick Lyden and colleagues in 2001. Prior to the NIHSS, during the late 1980s, several stroke-deficit rating scales were in use (e.g., University of Cincinnati scale, Canadian neurological scale, the Edinburgh-2 coma scale, and the Oxbury initial severity scale).

The NIHSS is composed of 11 items, each of which scores a specific ability between a 0 and 4. For each item, a score of 0 typically indicates normal function in that specific ability, while a higher score is indicative of some level of impairment.[1]

The individual scores from each item are summed in order to calculate a patient's total NIHSS score. The maximum possible score is 42, with the minimum score being a 0.[2] [3]

Score Stroke severity
0No stroke symptoms
1–4Minor stroke
5–15Moderate stroke
16–20Moderate to severe stroke
21–42Severe stroke

Performing the scale

While administering the NIHSS, it is important that the examiner does not coach or help with the assigned task. The examiner may demonstrate the commands to patients that are unable to comprehend verbal instructions; however, the score should reflect the patient's own ability. It is acceptable for the examiner to physically help the patient get into position to begin the test, but the examiner must not provide further assistance while the patient is attempting to complete the task.

For each item, the examiner should score the patient's first effort, and repeated attempts should not affect the patient's score. An exception to this rule exist in the language assessment (Item 9), in which the patient's best effort should be scored.[1]

Some of the items contain "Default Coma Scores". These scores are automatically assigned to patients that scored a 3 in Item 1a. Note that the NIHSS may fluctuate depending on the time.[4]

1. Level of consciousness (LOC)

Level of consciousness (LOC) testing is divided into three sections. The first LOC items test for the patient's responsiveness. The second LOC item is based on the patient's ability to answer questions that are verbally presented by the examiner. The final LOC sub-section is based on the patient's ability to follow verbal commands to perform simple task.

Although this item is broken into three parts, each sub-section is added to the final score as if it is its own item.[3]

A) LOC responsiveness

Scores for this item are assigned by a medical practitioner based on the stimuli required to arouse patient. The examiner should first assess if the patient is fully alert to his or her surroundings. If the patient is not completely alert, the examiner should attempt a verbal stimulus to arouse the patient. Failure of verbal stimuli indicates an attempt to arouse the patient via repeated physical stimuli. If none of these stimuli are successful in eliciting a response, the patient can be considered totally unresponsive.[3]

ScoreTest results
0Alert; Responsive
1Not alert; Verbally arousable or aroused by minor stimulation to obey, answer, or respond.
2Not alert; Only responsive to repeated or strong and painful stimuli
3Totally unresponsive; Responds only with reflexes or is areflexic

Notes

B) LOC questions

Patient is verbally asked his or her age and for the name of the current month.[3]

ScoreTest results
0Correctly answers both questions
1Correctly answers one question
2Does not correctly answer either question

Notes

C) LOC commands

The patient is instructed to first open and close his or her eyes and then grip and release his or her hand.[3]

ScoreTest results
0Correctly performs both tasks
1Correctly performs 1 task
2Does not correctly perform either task

Notes

2. Horizontal eye movement

Assesses ability for patient to track a pen or finger from side to side only using his or her eyes. This is designed to assess motor ability to gaze towards the hemisphere opposite of injury. This item is tested because conjugated eye deviation (CED) is present in approximately 20% of stroke cases. CED is more common in right hemispheric strokes and typically in lesions affecting the basal ganglia and temporoparietal cortex. Damage to these areas can result in decreased spatial attention and reduced control of eye movements.[5]

ScoreTest results
0Normal; Able to follow pen or finger to both sides
1Partial gaze palsy; gaze is abnormal in one or both eyes, but gaze is not totally paralyzed. Patient can gaze towards hemisphere of infarct, but cannot go past midline
2Total gaze paresis; gaze is fixed to one side

Notes

3. Visual field test

Assess the patient's vision in each visual fields. Each eye is tested individually, by covering one eye and then the other. Each upper and lower quadrant is tested by asking the patient to indicate how many fingers the investigator is presenting in each quadrant. The investigator should instruct the patient to maintain eye contact throughout this test, and not allow the patient to realign focus towards each stimulus. With the first eye covered, place a random number of fingers in each quadrant and ask the patient how many fingers are being presented. Repeat this testing for the opposite eye.[3]

ScoreTest results
0No vision loss
1Partial hemianopia or complete quadrantanopia; patient recognizes no visual stimulus in one specific quadrant
2Complete hemianopia; patient recognizes no visual stimulus in one half of the visual field
3Bilateral Blindness, including blindness from any cause

Notes

4. Facial palsy

Facial palsy is partial or complete paralysis of portions of the face. Typically this paralysis is most pronounced in the lower half of one facial side. However, depending on lesion location the paralysis may be present in other facial regions. While inspecting the symmetry of each facial expression the examiner should first instruct patient to show his or her teeth (or gums). Second, the patient should be asked to squeeze his or her eyes closed as hard as possible. After reopening his or her eyes, the patient is then instructed to raise his or her eyebrows.[6]

ScoreTest results
0Normal and symmetrical movement
1Minor paralysis; function is less than clearly normal, such as flattened nasolabial fold or minor asymmetry in smile
2Partial paralysis; particularly paralysis in lower face
3Complete facial Hemiparesis, total paralysis in upper and lower portions of one face side

Notes

5. Motor arm

With palm facing downwards, have the patient extend one arm 90 degrees out in front if the patient is sitting, and 45 degrees out in front if the patient is lying down. If necessary, help the patient get into the correct position. As soon as the patient's arm is in position the investigator should begin verbally counting down from 10 while simultaneously counting down on his or her fingers in full view of the patient. Observe to detect any downward arm drift prior to the end of the 10 seconds. Downward movement that occurs directly after the investigator places the patient's arm in position should not be considered downward drift. Repeat this test for the opposite arm. This item should be scored for the right and left arm individually, denoted as item 5a and 5b.[3]

ScoreTest results
0No arm drift; the arm remains in the initial position for the full 10 seconds
1Drift; the arm drifts to an intermediate position prior to the end of the full 10 seconds, but not at any point relies on a support
2Limited effort against gravity; the arm is able to obtain the starting position, but drifts down from the initial position to a physical support prior to the end of the 10 seconds
3No effort against gravity; the arm falls immediately after being helped to the initial position, however the patient is able to move the arm in some form (e.g. shoulder shrug)
4No movement; patient has no ability to enact voluntary movement in this arm

Notes

6. Motor leg

With the patient in the supine position, one leg is placed 30 degrees above horizontal. As soon as the patient's leg is in position the investigator should begin verbally counting down from 5 while simultaneously counting down on his or her fingers in full view of the patient. Observe any downward leg drift prior to the end of the 5 seconds. Downward movement that occurs directly after the investigator places the patient's leg in position should not be considered downward drift. Repeat this test for the opposite leg. Scores for this section should be recorded separately as 6a and 6b for the left and right legs respectively.[3]

ScoreTest results
0No leg drift; the leg remains in the initial position for the full 5 seconds
1Drift; the leg drifts to an intermediate position prior to the end of the full 5 seconds, but at no point touches the bed for support
2Limited effort against gravity; the leg is able to obtain the starting position, but drifts down from the initial position to physical support prior to the end of the 5 seconds
3No effort against gravity; the leg falls immediately after being helped to the initial position, however, the patient is able to move the leg in some form (e.g. hip flex)
4No movement; patient has no ability to enact voluntary movement in this leg

Notes

7. Limb ataxia

This test for the presence of a unilateral cerebellar lesion, and distinguishes a difference between general weakness and incoordination. The patient should be instructed to first touch his or her finger to the examiner's finger then move that finger back to his or her nose, repeat this movement 3-4 times for each hand. Next the patient should be instructed to move his or her heel up and down the shin of his or her opposite leg. This test should be repeated for the other leg as well.[3]

ScoreTest results
0Normal coordination; smooth and accurate movement
1Ataxia present in 1 limb; rigid and inaccurate movement in one limb
2Ataxia present in 2 or more limbs: rigid and inaccurate movement in both limbs on one side

Notes

8. Sensory

Sensory testing is performed via pinpricks in the proximal portion of all four limbs. While applying pinpricks, the investigator should ask whether or not the patient feels the pricks, and if he or she feels the pricks differently on one side when compared to the other side.[3]

ScoreTest results
0No evidence of sensory loss
1Mild-to-Moderate sensory loss; patient feels the pinprick, however he or she feels as if it is duller on one side
2Severe to total sensory loss on one side; patient is not aware he or she is being touched in all unilateral extremities

Notes

9. Language

This item measures the patient's language skills. After completing items 1-8, it is likely the investigator has gained an approximation of the patient's language skills; however, it is important to confirm this measurement at this time. The stroke scale includes a picture of a scenario, a list of simple sentences, a figure of assorted random objects, and a list of words. The patient should be asked to explain the scenario depicted in the first figure.

Next, the patient should read the list of sentences and name each of the objects depicted in the next figure. The scoring for this item should be based on both the results from the test performed in this item in addition to the language skills demonstrated up to this point in the stroke scale.[3]

ScoreTest results
0Normal; no obvious speech deficit
1Mild-to-moderate aphasia; detectable loss in fluency, however, the examiner should still be able to extract information from patient's speech
2Severe aphasia; all speech is fragmented, and examiner is unable to extract the figure's content from the patients speech.
3Unable to speak or understand speech

Notes

10. Speech

Dysarthria is the lack of motor skills required to produce understandable speech. Dysarthria is strictly a motor problem, and is not related to the patient's ability to comprehend speech. Strokes that cause dysarthria typically affect areas such as the anterior opercular, medial prefrontal and premotor, and anterior cingulate regions. These brain regions are vital in coordinating motor control of the tongue, throat, lips, and lungs.[7] To perform this item the patient is asked to read from the list of words provided with the stroke scale while the examiner observes the patient's articulation and clarity of speech.[3]

ScoreTest results
0Normal; clear and smooth speech
1Mild-to-moderate dysarthria; some slurring of speech, however the patient can be understood
2Severe dysarthria; speech is so slurred that he or she cannot be understood, or patients that cannot produce any speech

Notes

11. Extinction and inattention (f.k.a. neglect)

Sufficient information regarding this item may have been obtained by the examiner in items 1–10 to properly score the patient. However, if any ambiguity exist the examiner should test this item via a technique referred to as "double simultaneous stimulation".

Double simultaneous stimulation is performed by having the patient close his or her eyes and asking him or her to identify the side on which they are being touched by the examiner. During this time, the examiner is alternating between touching the patient on the right and left side. Next, the examiner touches the patient on both sides at the same time. This should be repeated on the patients face, arms, and legs.

To test extinction in vision, the examiner should hold up one finger in front of each of the patient's eyes and ask the patient to determine which finger is wiggling or if both are wiggling. The examiner should then alternate between wiggling each finger and wiggling both fingers at the same time.[3]

ScoreTest results
0Normal; patient correctly answers all questions
1Inattention on one side in one modality; visual, tactile, auditory, or spatial
2Hemi-inattention; does not recognize stimuli in more than one modality on the same side.

Notes

Usage

The NIHSS was designed to be a standardized and repeatable assessment of stroke patients utilized by large multi-center clinical trials.[8] Clinical researchers have widely accepted this scale due to its high scoring consistency, which has been demonstrated in inter-examiner and in test-retest scenarios.[9] Clinical research use of the NIHSS typically involves obtaining a baseline NIHSS score as soon as possible after onset of stroke symptoms[10] [11] The NIHSS is then repeated at regular intervals or after significant changes in patient condition. This history of scores can then be utilized to monitor the effectiveness of treatment methods and quantify a patient's improvement or decline.[12] [13] The NIHSS has also been used in a prospective observational study, to predict 3 month outcomes of patients with undernutrition during hospital stays directly after a stroke.[14]

NIHSS use in tPA eligibility

NIHSS has gained popularity as a clinical tool utilized in treatment planning. Tissue plasminogen activator (tPA), a type of thrombolysis, is one of the main options for treatment of acute ischemic strokes (the type of stroke caused by blood clots that are preventing blood flow within a cerebral artery).

The effectiveness and risk of tPA is strongly correlated with the delay between stroke onset and tPA delivery ("door-to-needle time"). Current standards recommend for tPA to be delivered within 4,5 hours of onset, while best results occur when treatment is delivered within 90 minutes of onset.[15]

Since the NIHSS has been established as a quick and consistent quantifier of stroke severity, many physicians have looked to NIHSS scores as indicators for tPA treatment.[16] This rapid assessment of stroke severity is targeted to reduce delay of tPA treatment. While some clinical trials have used minimum and maximum NIHSS scores to determine eligibility for acute treatment such as tPA, guidelines such as those from the American Heart Association / American Stroke Association urge against NIHSS scores being used as the sole reason for declaring a patient as ineligible for tPA treatment.[17]

NIHSS structure

In an effort to produce a complete neurological assessment the NIHSS was developed after extensive research and multiple iterations. The goal of the NIHSS was to accurately measure holistic neurological function by individually testing specific abilities. NIHSS total score is based on the summation of 4 factors. These factors are left and right motor function and left and right cortical function. The NIHSS assesses each of these specific functions by the stroke scale item listed in the chart below.[18]

Left cortical Right corticalRight motorLeft motor
LOC questionsHorizontal eye movementRight arm motorLeft arm motor
LOC commandsVisual fieldsRight legLeft leg
LanguageExtinction and inattentionDysarthria
Sensory

Modified National Institutes of Health Stroke Scale (mNIHSS)

The Modified NIH Stroke Scale (mNIHSS) is a shortened, validated version of the mNIHSS. It has been shown to be equally, if not more, accurate than the longer, older NIHSS. It removes questions 1A, 4, and 7. This makes the mNIHSS shorter and easier to use.

The mNIHSS predicts patients at high risk of hemorrhage if given tissue plasminogen activator (tPA) and which patients are likely to have good clinical outcomes.[19] The mNIHSS has also recently been shown to be taken without seeing the patient, and only using medical records. This potentially improves care while in the emergency room and the hospital, but also facilitates retrospective research.[20]

Accuracy

The National Institutes of Health Stroke Scale has been repeatedly validated as a tool for assessing stroke severity and as an excellent predictor for patient outcomes.[21] [22] [23] Severity of a stroke is heavily correlated with the volume of brain affected by the stroke; strokes affecting larger portions of the brain tend to have more detrimental effects.[24] NIHSS scores have been found to be reliable predictors of damaged brain volume, with a smaller NIHSS score indicating a smaller lesion volume.[25]

Effect of stroke location on NIHSS prediction of stroke severity

The NIHSS places 7 of the possible 42 points on abilities that require verbal skills; 2 points from the LOC questions, 2 points from LOC commands, and 3 points from the Language item. The NIHSS only awards 2 points for extinction and inattention.[26] Approximately 98% of humans have verbal processing take place in the left hemisphere, indicating that the NIHSS places more value on deficits in the left hemisphere. This results in lesions receiving a higher (worse) score when occurring in the left hemisphere, compared to lesions of equal size in the right hemisphere. Due to this emphasis, the NIHSS is a better predictor of lesion volume in the strokes occurring within the left cerebral hemisphere.[17]

NIHSS as predictor of patient outcomes

The NIHSS has been found to be an excellent predictor of patient outcomes. A baseline NIHSS score greater than 16 indicates a strong probability of patient death, while a baseline NIHSS score less than 6 indicates a strong probability of a good recovery. On average, an increase of 1 point in a patient's NIHSS score decreases the likelihood of an excellent outcome by 17%.[27] However, correlation between functional recovery and NIHSS scores was weaker when the stroke was isolated to the cortex.[25]

Other stroke-related scores

References

[28]

Notes and References

  1. National Institutes of Health, National Institute of Neurological Disorders and Stroke. Stroke Scale. https://www.ninds.nih.gov/sites/default/files/documents/NIH-Stroke-Scale_updatedFeb2024_508.pdf.
  2. NIH Stroke Scale Training, Part 2. Basic Instruction. Department of Health and Human Services, National Institute of Neurological Disorders and Stroke. The National Institute of Neurological Disorders and Stroke (NINDS) Version 2.0
  3. Hage V . 2011 . The NIH stroke scale: a window into neurological status . Nursing Spectrum . 24 . 15. 44–49 .
  4. Web site: Costalat . Doctor . 13 October 2021 . 2021 . 13 October 2021 . SLICE Worldwide 2021 - Failed Thrombectomy . Master & Fellows . English . 13 October 2021.
  5. Singer O, Humpich M, Laufs H, Lanfermann H, Steinmetz H, Neumann-Haefelin T . 2006 . Conjugate eye deviation in acute stroke: incidence, hemispheric asymmetry, and lesion pattern . Stroke . 37 . 11. 2726–2732 . 10.1161/01.str.0000244809.67376.10 . 17008621. free .
  6. Schimmel M, Leemann B, Christou P, Kiliaridis S, Herrmann F, Muller F. Quantitative assessment of facial muscle impairment in patients with hemispheric stroke. Journal of Oral Rehabilitation [serial online]. n.d.;NOV, 2011, 38.11, p800-p809, 10p.
  7. Okuda B, Kawabata K, Tachibana H, Sugita M . 1999 . Cerebral blood flow in pure dysarthria: role of frontal cortical hypoperfusion . Stroke . 30 . 1. 109–113 . 10.1161/01.str.30.1.109. 9880397 .
  8. Brott T, Adams HP, Olinger CP, etal . 1989 . Measurements of acute cerebral infarction—a clinical examination scale . Stroke . 20 . 7. 864–70 . 10.1161/01.str.20.7.864. 2749846 .
  9. Goldstein LB, Bartels C, Davis JN . 1989 . Interrater reliability of the NIH Stroke Scale . Arch Neurol . 46 . 6. 660–662 . 10.1001/archneur.1989.00520420080026. 2730378 .
  10. Clark WM, Wissman S, Albers GW, Jhamandas JH, Madden KP, Hamilton S . 1999 . Recombinant tissue-type plasminogen activator (alteplase) for ischemic stroke 3 to 5 hours after symptom onset: the ATLANTIS study: a randomized con- trolled trial . JAMA . 282 . 21. 2019–2026 . 10.1001/jama.282.21.2019. 10591384 .
  11. Del Zoppo GJ, Higashida RT, Furlan AJ, Pessin MS, Rowley HA, Gent M . 1998 . PROACT: a phase II randomized trial of recombinant pro-urokinase by direct arterial delivery in acute middle cerebral artery stroke . Stroke . 29 . 1. 4–11 . 10.1161/01.str.29.1.4. 9445320 . free .
  12. Furlan A, Higashida R, Wechsler L, Gent M, Rowley H, Kase C, Pessin M, Ahuja A, Callahan F, Clark WM, Silver F, Rivera F . 1999 . Intra-arterial prourokinase for ischemic stroke: the PROACT II study: a randomized controlled trial . JAMA . 282 . 21. 2003–2011 . 10.1001/jama.282.21.2003. 10591382 .
  13. Lewandowski CA, Frankel M, Tomsick TA, Broderick J, Frey J, Clark W, Starkman S, Grotta J, Spilker J, Khoury J, Brott T . 1999 . Combined intra- venous and intra-arterial r-TPA versus intra-arterial therapy of acute ischemic stroke. Emergency Management of Stroke (EMS) Bridging Trial . Stroke . 30 . 12. 2598–2605 . 10.1161/01.str.30.12.2598. 10582984 . free .
  14. 18195138 . 2008 . Yoo . SH . Kim . JS . Kwon . SU . Yun . SC . Koh . JY . Kang . DW . Undernutrition as a Predictor of Poor Clinical Outcomes in Acute Ischemic Stroke Patients. . 65 . 1 . 39–43 . Archives of Neurology . 10.1001/archneurol.2007.12.
  15. Eissa A, Krass I, Bajorek B. "Optimizing the management of acute ischaemic stroke: a review of the utilization of intravenous recombinant tissue plasminogen activator (tPA). Journal of Clinical Pharmacy & Therapeutics December 2012;37(6):620-629.
  16. Mishra . NK . Lyden . P . Grotta . JC . Lees . KR . 2010 . Thrombolysis Is Associated With Consistent Functional Improvement Across Baseline Stroke Severity: A Comparison of Outcomes in Patients From the Virtual International Stroke Trials Archive (VISTA) . Stroke . 41 . 6 . 2612–2617 . 10.1161/strokeaha.110.589317 . 20947852 . free.
  17. Fink JN, Selim MH, Kumar S, etal . 2002 . Is the association of National Institutes of Health Stroke Scale scores and acute magnetic resonance imaging stroke volume equal for pa- tients with right- and left-hemisphere ischemic stroke? . Stroke . 33 . 4 . 954–8 . 10.1161/01.str.0000013069.24300.1d . 11935043 . free.
  18. Lyden P, Lu M, Jackson C, Marler J, Kothari R, Brott T, Zivin J . 1999 . Underlying structure of the National Institutes of Health Stroke Scale: results of a factor analysis . Stroke . 30 . 11. 2347–2354 . 10.1161/01.str.30.11.2347. 10548669 .
  19. Lyden PD, Lu M, Levine SR, Brott TG, Broderick J, NINDS rtPA Stroke Study Group. . 2001 . A modified National Institutes of Health Stroke Scale for use in stroke clinical trials: preliminary reliability and validity.. Stroke . 32 . 6 . 1310–7 . 11387492 . 10.1161/01.str.32.6.1310. free .
  20. Kasner SE, Cucchiara BL, McGarvey ML, Luciano JM, Liebeskind DS, Chalela JA . 2003 . Modified National Institutes of Health Stroke Scale can be estimated from medical records. . Stroke . 34 . 2 . 568–70 . 12574577 . 10.1161/01.str.0000052630.11159.25. free .
  21. Muir KW, Weir CJ, Murray GD, Povey C, Lees KR . 1996 . Comparison of neurological scales and scoring systems for acute stroke prognosis . Stroke . 27 . 10. 1817–1820 . 10.1161/01.str.27.10.1817. 8841337 .
  22. Frankel MR, Morgenstern LB, Kwiatkowski T, Lu M, Tilley BC, Broderick JP, Libman R, Levine SR, Brott T . 2000 . Predicting prognosis after stroke: a placebo group analysis from the National Institute of Neurological Disorders and Stroke rt-PA Stroke Trial . Neurology . 55 . 7. 952–959 . 10.1212/wnl.55.7.952. 11061250 . 39939549 .
  23. Dehaan R, Horn J, Limburg M, etal. 1993 . A comparison of 5 stroke scales with measures of disability, handicap, and quality-of-life . Stroke . 24 . 8. 1178–81 . 10.1161/01.str.24.8.1178. 8342193 . free .
  24. Weimar C, Konig I, Kraywinkel K, Ziegler A, Diener H . 2004. Age and national institutes of health stroke scale score within 6 hours after onset are accurate predictors of outcome after cerebral ischemia - Development and external validation of prognostic models . Stroke . 35 . 1. 158–162 . 10.1161/01.str.0000106761.94985.8b . 14684776. free .
  25. Glymour M, Berkman L, Ertel K, Fay M, Glass T, Furie K . 2007 . Lesion characteristics, NIH Stroke Scale, and functional recovery after stroke . American Journal of Physical Medicine & Rehabilitation . 86 . 9. 725–733 . 10.1097/phm.0b013e31813e0a32. 17709996 . 29378035 .
  26. Woo D, Broderick JP, Kothari RU, Lu M, Brott T, Lyden PD, Marler JR, Grotta JC . 1999 . Does the National Institutes of Health Stroke Scale favor left hemisphere strokes? . Stroke . 30 . 11. 2355–2359 . 10.1161/01.str.30.11.2355. 10548670 . free .
  27. Adams H, Davis P, Hansen M, etal . 1999. Baseline NIH Stroke Scale score strongly predicts outcome after stroke - A report of the Trial of Org 10172 in Acute Stroke Treatment (TOAST) . Neurology . 53 . 1. 126–131 . 10.1212/wnl.53.1.126. 10408548. 20176582.
  28. 3426834 . 20828876 . 10.1016/j.annemergmed.2010.06.564 . 57 . 1 . Zero on the NIHSS does not equal the absence of stroke . 2011 . Ann Emerg Med . 42–5 . Martin-Schild S, Albright KC, Tanksley J, Pandav V, Jones EB, Grotta JC, Savitz SI .