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NOTE. Demonstrable organic pathology commensurate with the functional loss will be required. The concentric contraction ratings require contraction within the stated degrees, temporally; the nasal contraction may be less. The alternative ratings are to be employed when there is ratable defect of visual acuity, or a different impairment of the visual field in the other eye. Concentric contraction resulting from demonstrable organic pathology to 5 degrees or less will be considered on a parity with reduction of central visual acuity to 5/200 or less for all purposes including entitlement under subparagraph (1), 38 U.S.C. 314; not, however, for the purpose of subparagraph (k). Entitlement on account of blindness requiring regular aid and attendance, subparagraph (m), will continue to be determined on the facts in the individual case.

20

FUNCTION

NOTE. Correct diagnosis reflecting disease or injury should be cited.

6090 Muscle function, ocular, im

6091

pairment of

Producing diplopia in 19-20

rectangles

Rate as 5/200.

Producing diplopia in 17-18

rectangles

Rate as 10/200.

Producing diplopia in 14-16

rectangles

Rate as 15/200.

Producing diplopia in 12-13

rectangles

Rate as 20/200.

Producing diplopia in 9-11

rectangles

Rate as 20/100.

Producing diplopia in 6-8

rectangles

Rate as 20/70.

Producing diplopia in 3-5

rectangles

Rate as 20/50.

Producing diplopia in 0-2

rectangles

Rate as 20/40.

NOTE. The ratings under diagnostic Code 6090 are to be applied only to the poorer eye if both have ratable impairment of visual acuity or visual field; if only one eye has a ratable impairment, to that eye, but not in combination with any other eye rating.

Symblepharon

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paired efficiency (A, B, C, D, E, or F) will be determined by intersecting the horlzontal row appropriate for percentage of discrimination and the vertical column appropriate to the speech reception decibel loss; thus, with a speech reception decibel loss of 52 db and a percentage discrimination of 72 percent, the literal designation is "D"; if the speech reception decibel loss is 52 db and the percentage discrimination is 70 percent, the literal designation is "E".

(b) The percentage evaluation will be found from table II by intersecting the horizontal row appropriate for the literal designation for the ear having the better hearing and the vertical column appropriate to the literal designation for the ear having the poorer hearing. For example, if the better ear has a literal designation of "B" and the poorer ear has a literal designation of "C," the percentage evaluation is in the second horizontal row from the bottom and in the third vertical column from the right and is 10 percent.

(c) If the results of pure tone audiometry (either pure tone air conduction or Galvanic Skin Response, PGSR) are used, the equivalent literal designation for each ear, separately, will be ascertained from table II, and the percentage evaluation determined in the same manner as for speech reception impairment in paragraph (b) of this section. For example, if the average pure tone decibel loss for the frequencies 500, 1,000, and 2,000 is not more than 45 db and there is no loss more than 60 db for any of these three frequencies, the equivalent literal designation is "C"; if in the other ear, the average is not more than 67 db, and there is no loss more than 80 db, the equivalent literal designation is "D". The percentage evaluation is therefore found in the horizontal row opposite "C", and in the vertical column under "D", and is 20 percent. Note that if in the first instance any of the 3 frequencies has a loss of more than 60 db, or in the second instance more than 80 db, the literal designation will be higher, i.e., further from "A" in the alphabetical series.

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§4.87a Diagnostic codes based upon speech reception impairment literal designation.

6277 Rated Column F, One Ear Row
F, Other Ear Table II

6278 Rated Column F, One Ear Row
E, Other Ear Table II
6279 Rated Column F, One Ear Row
D, Other Ear Table II
6280 Rated Column F, One Ear Row
C, Other Ear Table II
6281 Rated Column F, One Ear Row
B, Other Ear Table II

6291 Rated Column D, One Ear Row
A, Other Ear Table II

6292 Rated Column C, One Ear Row
C. Other Ear Table II
6293 Rated Column C, One Ear Row
B, Other Ear Table II
6294 Rated Column C, One Ear Row
A, Other Ear Table II
6295 Rated Column B, One Ear Row
B, Other Ear Table II
6296 Rated Column B, One Ear Row
A, Other Ear Table II
6297 Rated Column A, One Ear Row
A, Other Ear Table II

§ 4.87b Schedule of ratings other

6282 Rated Column F, One Ear Row A, Other Ear Table II 6283 Rated Column E, One Ear Row E, Other Ear Table II 6284 Rated Column E, One Ear Row D, Other Ear Table II 6285 Rated Column E, One Ear Row C, Other Ear Table II

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6286 Rated Column E, One Ear Row B, Other Ear Table II

6287 Rated Column E, One Ear Row A, Other Ear Table II

6288 Rated Column D, One Ear Row D, Other Ear Table II

6289 Rated Column D, One Ear Row C, Other Ear Table II

6290 Rated Column D, One Ear Row B, Other Ear Table II

NOTE. Anatomical or pathological basis required for the ratings under diagnostic codes 6275 and 6276.

SYSTEMIC CONDITIONS

§ 4.88 Malaria.

In rating disability from malaria, once identified by clinical and laboratory methods, or by clinical methods alone

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Clinically active so as to re-
quire hospital treatment for
a contemplated or elapsed
period of 14 days or more;
or with a combination of
cerebral symptoms, enlarged
spleen, anemia or other se-
vere symptoms---
Clinically active so as to re-

quire intensive treatment;
recently active with 3 or
more relapses over past 6
months; or old cases with
marked general impairment
of health..

Recently active with 2 relapses

in past 6 months; or old cases with anemia..

Recently active with one re

lapse in the past year; or old cases with moderate disability

NOTE (1). The evaluations under Code 6304 are to be assigned on the basis of dates and frequency of recurrences and relapses and severity of significant

100

100

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Rating

residuals, if any, based on the clinical records of the service department or other acceptable evidence relating to the period of service, or on medical evidence relating to the period after discharge, recording sufficient clinical findings, when considered in accordance with all other data of record, to support the conclusion that there exists a compensable or higher degree of disability from malaria. Hereafter, service connection will not be conceded based on notation in service records of history alone furnished by the veteran, nor will compensable ratings be assigned based on the veteran's unsupported claim or statement; however, determinations heretofore made will not be reversed on the basis of this change in policy. The evidence of others under oath may be accepted to establish frequency of relapses or recurrences over a period of 1 year only, from date of last medically confirmed relapse or recurrence in service or subsequently.

NOTE (2). When evaluations are based on frequency of recurrences or relapses only, they will be assigned for a period of 1 year only from date of discharge or date established by medical evidence of record. At the expiration of this period, if medical evidence warranting an extension is not of record, the veteran will be notified that his compensation will be discontinued unless he submits evidence from a physician showing recurrent attacks or other disabling effects of malaria. After a malaria rating has run 24 months, an extension, if warranted, will carry ending date at expiration of 36 months from initial date of compensable rating. When this rating is assigned, veteran will be notified of ending date and of requirement that, to have rating continued or resumed after that date, he must report to Veterans Administration hospital, or outpatient clinic, or to a Veterans Administration fee-basis physician during an actual relapse of the disease. Following the expiration of the 36 months' period and the veteran's compliance with the requirement to report as indicated in this note, a prepared slide of the veteran's blood smear will be read in the

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