Loading

Adult scoliosis: classification based on the L3-L5 segment

Research Article | Open Access | Volume 9 | Issue 1

  • 1. Unit, Universitary Hospitalary Complex. Santiago de Compostela, Spain
  • 2. Department of Traumatology, University of Santiago de Compostela, Spain
+ Show More - Show Less
Corresponding Authors
Máximo-Alberto Díez-Ulloa, Servicio de Traumatología y Cirugía Ortopédica, Hospital Clinico Universitario, CHU Santiago de Compostela, Trav da Choupana s/n. 15706 Santiago de Compostela (A Coruna), Spain, Email: maximoalberto.diez@usc.es
ABSTRACT

1.1. Study Design: Retrospective review of a case series.

1.2. Objective: Define objective parameters to differentiate between Adults Degenerative Scoliosis (ADS), and Adult Idiopathic Scoliosis (AdIS). These are at the L3-L5 segment. 1.3.

Methods: A series of 53 adult scoliosis (mean age 55 y.o., median 57 y.o. range: 20-84 y.o.), was studied. Variables: age, curve parameters (Cobb, end vertebra), coronal and sagittal balance, spinopelvic parameters, and L3-L5 parameters (distance from the center of the disc to CSVL, and endplate coronal tilt).

Statistical study: R package software, some variables not normal distribution, non-parametric tests. Approved by the IRB. 1.4.

Results: Distance of L3-L4 disc (18 mm; 2-52) showed a bimodal distribution that also correlated to spinopelvic parameters: if 15mm or less, then PT 22º±8º; if > 15 mm, then PT 32º±17º (p=0.04 U Mann-Whitney). L4 endplate tilt inversely correlates to SS (Pearson -0.3; p<0.01), and positively to PT (Pearson 0.4;p=0.002) L3-L5 segment helps differentiate ADS from AdIS.

1.5. Conclusions: Distance of the center of the disc L3-L4 to the central sacral line is an objective parameter to differentiate ADS from AdIS.

It also correlates with compensatory mechanisms (PT), with statistical differences in PT between types of adult scoliosis.

KEYWORDS

 Spine;

Deformity;

Scoliosis;

Adult Scoliosis;

Idiopathic Scoliosis;

Degenerative Scoliosis;

Balance;

Classification

CITATION

DÍEZ-ULLOA MA, DÍEZ-SANCHIDRIAN E, DOMIGO-RODRIGUEZ L, OTERO-TORRÓN B, PEREIROS-PARADA A, et al. (2022) Adult scoliosis: classification based on the L3-L5 segment. JSM Neurosurg Spine 9(1): 1105.

ABBREVIATIONS

ADS: Adult Degenerative Scoliosis; AdIS: Adult Idiopathic Scoliosis; CSVL: Central Sacral Vertical Line; SVA: Sacral Vertical Axis; PI: Pelvic Incidence; PT: Pelvic Tilt; SS: Sacral Slope

INTRODUCTION

The pathogenesis of adult scoliosis is a deformity from the collapse of the spine that bends due to asymmetrical changes at the vertebral functional units, especially at the facet joints; this type being de novo adult degenerative scoliosis (ADS); or else, the evolution of an adolescent idiopathic curve (AdIS), in which, usually the symptomatic decompensation arises from distal junctional problems. Aebi called the first situation adult scoliosis type I and the second adult scoliosis type II [1]. This differentiation probably has implications on surgical planning, but the quest for criteria to differentiate between both types has not been successful.

It is for granted, on differentiating ADS from AdIS, that ADS has low Cobb angles, involves few vertebral bodies that are not wedge-shaped, and then develops no thoracic compensatory curve [2]. But, in real life, differentiation between both types is not easy. Even more, the intra-observer agreement is moderate to substantial, but the inter-observer one is just fair [3].

So, those theoretical items set to differentiate are of some (not high), value when the same radiographies are evaluated twice by the same observer, but they have hardly any value when different observers classify. This fact makes the problem even bigger as individual observers do not perceive this low reliability unless challenged by the judgment of others.

When you need to evaluate the radiographies of an adult patient with scoliosis with a lumbar curve, the question arises: how did we get to this point? That is, we try to look back at the pathogenesis.

Why the L3-L5 segment?

Once having said that, degenerative changes responsible for ADS usually happen at L3-L4 or else L4-L5 levels, as the L5-S1 (also degenerated), is deep in the pelvis, with L5 tied by iliolumbar ligaments and thus making vertebral rotation not possible; also, from the other pathogenic pathway, the end vertebra in AdIS curves is either L3 or L4, so that junctional issues happen at L3-L4 or else L4-L5 levels. Hence, at the L3-L5 segment in ADS, we will see the apical disc, which is horizontal and away from the central sacral line. On the other hand, in patients of AdIS, we will see the junction, with an end vertebra close to the midline (central sacral vertical line, CSVL), and a slanted disc between theend vertebra and the neutral (sometimes the same as the stable one, see Figures 1 and 2).

Figures 1

Figure 1 Adult Idiopathic Scoliosis.

Figure 1 Adult Idiopathic Scoliosis.

Figure2 

Figure 2 Adult Degenerative Scoliosis.

Figure 2 Adult Degenerative Scoliosis.

Figure 3

Figure 3 Distance L3-L4 to CSVL.

Figure 3 Distance L3-L4 to CSVL.

Figure 4

Figure 4 Distance L3-L4 to CSVL versus Pelvic Tilt.

Figure 4 Distance L3-L4 to CSVL versus Pelvic Tilt.

Hypothesis

At the L3-L5 segment, there are objective data to differentiate between ADS and AdIS.

Secondary hypothesis

These different pathogenetic pathways result in a different balance, the ADS being imbalanced due to that degenerative collapse at the lower lumbar spine.

MATERIALS AND METHODS

A series of 60 patients had surgery for scoliosis affecting the lumbar spine, all by the same surgeon. Seven patients had poor imaging (not possible to see the center of rotation of the hips in lateral radiographies), and had to be left out. So 53 remained and were considered for the study. Seven had had surgery before 45 years of age, all seven with a thoracic curve; besides, another 14 patients had thoracic scoliosis (curve > 10º), and surgery older than 45 years of age. Variables: age, thoracic curve (Cobb, upper and lower limits, and apex), lumbar curve (Cobb, upper and lower limits, and apex), lumbosacral curve (Cobb, upper and lower limits, and apex), T1 and L1 balance both coronal and sagittal (millimeters from CSVL and sacral vertical axis -SVArespectively), spinopelvic parameters (pelvic incidence -PI-, pelvic tilt -PT- and sacral slope -SS-), and L3-L5 parameters (distance of the center of L3-L4 and L4-L5 discs to CSL in AP view; the tilt of each endplate of these discs: inferior endplate L3, superior & inferior endplates L4 and superior endplate L5). Statistics: R package software, non-parametrical tests as non all variables had a normal distribution. This research has got the approval of the Institutional Review Board (Ethical Committee for Clinical Research of the Hospital).

RESULTS

Data from 53 valid patients: age 55y.o. (20-84 y., median 57 y.), thoracic curve (present in 21 out of the 53), 34º (0-91º), lumbar curve (in 48 out of the 53), 32º (0-73º), lumbosacral curve 17º (0- 31º). Spinopelvic parameters: PI 60º (21-90º), SS 34º (7-61º), PT 26º (6-67º). L3- L5 variables: distance L3-L4 disc to CSL 18 mm (2-52 mm) showing a bimodal distribution, distance L4-L5 disc to CSL 8 mm (0-43 mm), tilt L3 inferior endplate 13º (1-32º), tilt L4 superior endplate 13º (0-31º), tilt L4 inferior endplate 13º (0- 32º), tilt L5 superior endplate 8º (0-30º). The results showed a correlation between the endplate tilt at the L3-L5 segment versus the spinopelvic parameters (see Table 1).

Table 1: L3-L5 endplate tilt vs. spinopelvic parameters: Pearson correlation and p values in brackets.

Endplate tilt (º)

SS

PT

Inferior L3

-0.228 (<0.05)

NS

Superior L4

-0.364 (0.007)

0.421 (0.002)

Inferior L4

-0.31 (0.002)

0.41 (0.002)

Abbreviations: PT: Pelvic Tilt; SS: Sacral Slope; NS: not significant.

No differentiation could be made based on the stratification of data. The analysis of results showed: a) disc distance from CSL at the L3-L5 segment vs. spinopelvic parameters showed a bimodal distribution at the L3L4 disc with a mean of 17.86 mm and a median of 14.15 mm. If a cut-point of 15 mm is selected, we can differentiate two groups regarding PT, if < 15 mm then PT 22º+8º, but if >15mm then PT 32º+17º (p=0.042; U Mann-Whitney). In the overall analysis of the results, distance L3-L4 to CSL vs. PT had a positive correlation (Pearson 0.32; R-square=0.105, p=0.018) (see Figures 1 and 2).

DISCUSSION

The first question is why classify adult scoliosis. That is not simply an academic action; it has been a must for surgeons, the goals being: systematic categorization, prognostic information based on natural history, correlation with health status, and guiding optimal care [4]. Aside from the descriptive, purely nominal classifications, the rationale is a basis for the management. Sometimes, like the one described by Kuntz [5], many items are considered (up to 17 in the coronal plane and 21 in the sagittal), to focus on the NUSA (neutral upright spinal alignment), which means balance. And balance is the guiding thread in the paper by Nakashima [6], again striving for an energy-sparing environment to avoid unnecessary fatigue. All this becomes especially important in adults, and thus another methodology is evolving from adolescent classification by adding relevant modifiers for the adult deformities setting: the fractional lumbosacral curve and, again, balance, but in the form of a global alignment, a step beyond spinopelvic parameters [7].

Due to its aggressiveness, surgery in adult scoliosis might be fraught with perioperative complications. Then, another classification comes out by Silva and Lenke to design the most overall profitable stepwise approach in surgical planning [8]. And finally, but probably not the last to come, AO Spine proposes a “comprehensive patient evaluation” (quote) instead of a classification [9]. This evaluation comprises general health (both comorbidities and demographics, including social support), spine-specific status (both health, including pain, quality of life, expectations, and previous surgery; and neurologic status), imaging (both radiographies and MRI), and type of deformity.

Type of deformity comes into play as a feature for understanding the patient spine deformity, and the distinction between types (ADS, AdIS), has shown to be an unclear field, mainly because although an acceptable intra-rater agreement exists, that was not the case with inter-rater one [3].

That situation, from our perspective, is a deceptive problem as it is not perceived as such until confronted by peers. And there is a need to define some clear-cut criteria to differentiate among curve types.

When looking for a rationale for this differentiation, we focused on the pathogeny. Then, addressing the problem: on one side, we have a “crack” in the spine at a junction, with rotatory subluxation, canal encroachment, and one mechanically vulnerable point, whereas, on the other, we have spondylosis with huge syndesmophytes, causing neurogenic claudication to the lower limbs sometimes not relieved by sitting [10], and perhaps, a balance problem of the trunk, but not with one unstable vertebral functional unit.

Our results clearly show two different types of lumbar adult scoliotic curves regarding distance to CSVL from the L3-L4 disc, as this variable shows a bimodal distribution with statistically significant differences between them. Besides, this same variable correlates to PT, which is known to be an important compensatory mechanism for sagittal imbalance, with a different mean for PT in any of the two types of the bimodal distribution of the distance L3-L4 disc to CSVL. And, going a step further, the PT value in one of them is below the consensual level for deformity in itself (PT=25, after Schwab)[11] while in the other is quite above; that is, one is pathological versus the other, which is not. Thence, we describe a variable with little margin for error that can give information about the kind (not just type), of deformity we are managing.

And the distinction happens in the L3-L5 segment, where the natural history differs in ADS versus AdIS. Whether these types match may be a question for further debate, but it seems an at least acceptable assumption. It seems clear also that there are different pathogenic pathways to get to a twisted spine in an adult patient, the two main groups being: a) those already scoliotic patients since adolescence in which, due to the degeneration of discs and then the spine, an asymptomatic situation becomes symptomatic; b) another one would be those patients in which without any previous curve, a whole degenerative collapse brings about the deformity [1]. As we said before, research to distinguish ADS patients from AdIS patients with standard variables obtained no positive outcome [3].

Of note is that, probably due to the rib cage and, besides, the biomechanical environment with higher loads and demands in the lumbar spine, adult scoliosis is a problem of the lumbar spine, the thoracic spine especially being concomitantly affected by aging and kyphosis, which adds to the lumbar issues sometimes. Symptoms in patients with adult scoliosis arise in the lumbar spine, whether directly (root compression), or indirectly (trunk imbalance). And this trunk imbalance has two main components: spine deformity and sarcopenia, which makes the body unable to maintain proper balance. Once having said that, now the second question is whether surgical planning is affected by this different pathogenesis. And we think it should: on the one hand, given there is a definite unstable short area, it is possible to address only this segment in some patients, with aggressive work in the disc space and facets; on the other, a multilevel degeneration problem is more prone to cause a disbalance of the trunk, or else, canal stenosis in a more stable biomechanical environment in which localized decompressions without fusion or short fusions (one or two levels), could be the best planning for one specific patient. Besides, be a need for a global realignment, the L4-L5 disc usually has to be addressed as part of the restoration of lordosis, but the L3-L4 disc might also need it if there is a junctional subluxation; otherwise, a weak point in the anterior column could act as a stress riser and facilitate pseudoarthrosis. In the same line of reasoning, it seems not advisable to plan a pure decompressive procedure on an unstable level, but it could be wise to do an instrumented fusion of that single level.

All this reasoning goes in the same line as the paper of Li [12], which addresses the anterior column in a more aggressive way LLIF), may change the planning. Thus, as a result of our research, sometimes the L3-L4 disc needs stable anterior support, not necessary for lordosis, which usually lies in L4-S1, but just for further stabilization of the segment. We could spare the L5-S1 segment fusion after a thorough anterior reconstruction by LLIF L3-L4.

We propose some such parameters, the distance to CSVL and endplate tilt, both at the L3-L5 segment, which are not usually measured when planning for these patients, are capable of differentiating two kinds of adult scoliosis. And, for sure, a classification after them, due to their simplicity (a distance and a tilt), will have high intra-observer reliability and a much better interobserver than in other series [3].

Although we did not formally address intra-observer and interobserver reliabilities in our series, there was a group of radiographies (the 20 patients that were the first to be measured), in which we repeated the measurements (disregarding the 20 initial values). That served both as training and a way to diminish this intra-observer variability.

Nevertheless, the initial values showed almost identical results compared to the repeated ones. Besides, most measurements were done collectively and by on-site consensus, so there was no role for interobserver variability. The objective was not a classification to be validated but to find objective parameters to foster interobserver reliability in the existing ones [1,9].

CONCLUSIONS

1) We have found a criterion to differentiate two groups in adult scoliosis patients regarding PT: distance from the center of the L3-L4 disc to CSL.

2) L4 endplates tilt correlates with compensation mechanisms (SS vs. PT).

ACKNOWLEDGEMENTS

Paper presented at the Spanish Spine Society (GEER) National Meeting 2019.

CONFLICT OF INTEREST

The authors declare no conflict of interest related to the topic of the manuscript or any conflict of interest exists.

REFERENCES

1. Aebi M. The Adult Scoliosis. Eur Spine J. 2005;14: 925-948.

2. York PJ, Kim HJ. Degenerative Scoliosis. Curr Rev Musculoskeletal Med. 2017; 10: 547-558.

3. Guler UO, Yuksel S, Domingo-Sabat M, Pellise F, Pérez-Grueso FJS, Obeid I, et al. Analysis of the Reliability of the Surgeons Ability to Differentiate between Idiopathic and Degenerative Spinal Deformity in Adults Radiologically. What Descriptive Parameters Help Them Decide? Eur Spine J. 2016; 25: 2401-2407.

4. Lowe T, Berven SH, Schwab FJ, Bridwell KH. The SRS classification for adult spinal deformity: building on the King/Moe and Lenke classifications systems. Spine (Phila Pa 1976). 2006; 31: S119-S125.

5. Kuntz C, Shaffrey CI, Ondra SL, Durrani AA, Mummaneni PV, Levin LS, et al. Spinal deformity: a new classification derived from neutral upright spinal alignment measurements in asymptomatic juvenile, adolescent, adult, and geriatric individuals. Neurosurgery. 2008; 63: 25-39.

6. Nakashima H, Kawakami N, Ohara T, Saito T, Tauchi R, Imagama S. A new global spinal balance classification based on individual pelvic anatomical measurements in patients with adult spinal deformity. Spine (Phila Pa 1976). 2020; 46: 223-231.

7. Lin JD, Osorio JA, Baum GR, Menger RP, Reid PC, Dyrszka MD, et al. A new modular radiographic classification of adult idiopathic scoliosis as an extension of the Lenke classification of adolescent idiopathic scoliosis. Spine Deform. 2021; 9: 175-183.

8. Silva FE, Lenke LG. Adult degenerative scoliosis: evaluation and management. Neurosurg Focus. 2010; 28: E1.

9. Naresh-Babu J, Kwan KYH, Wu Y, Yilgor C, Alanay A, Cheung KMC, et al. AO Spine adult spinal deformity patient profile: a paradigm shift in comprehensive patient evaluation in order to optimize treatment and improve patient care. Global Spine J. 2021.

10.Grubb SA, Lipscomb HJ, Coonrad RW. Degenerative Adult Onset Scoliosis. Spine. 1988; 13: 241-245.

11.Schwab F, Ungar B, Blondel B, Buchowski J, Coe J, Deinlein D, et al. Scoliosis Research Society-Schwab Adult Spine Deformity Classification: a validation study. Spine (Phila Pa 1976). 2012; 37: 1077-1082.

12.Li H, Xu Z, Li F, Chen Q. Does Lateral Lumbar Interbody Fusion Decrease the Grading of Lenke-Silva Classification and Determine the Optimal Fusion Level in Severe Adult Degenerative Scoliosis? World Neurosurg. 2020; 139: e335-e344

DÍEZ-ULLOA MA, DÍEZ-SANCHIDRIAN E, DOMIGO-RODRIGUEZ L, OTERO-TORRÓN B, PEREIROS-PARADA A, et al. (2022) Adult scoliosis: classification based on the L3-L5 segment. JSM Neurosurg Spine 9(1): 1105.

Received : 08 May 2022
Accepted : 26 May 2022
Published : 30 May 2022
Journals
Annals of Otolaryngology and Rhinology
ISSN : 2379-948X
Launched : 2014
JSM Schizophrenia
Launched : 2016
Journal of Nausea
Launched : 2020
JSM Internal Medicine
Launched : 2016
JSM Hepatitis
Launched : 2016
JSM Oro Facial Surgeries
ISSN : 2578-3211
Launched : 2016
Journal of Human Nutrition and Food Science
ISSN : 2333-6706
Launched : 2013
JSM Regenerative Medicine and Bioengineering
ISSN : 2379-0490
Launched : 2013
JSM Spine
ISSN : 2578-3181
Launched : 2016
Archives of Palliative Care
ISSN : 2573-1165
Launched : 2016
JSM Nutritional Disorders
ISSN : 2578-3203
Launched : 2017
Annals of Neurodegenerative Disorders
ISSN : 2476-2032
Launched : 2016
Journal of Fever
ISSN : 2641-7782
Launched : 2017
JSM Bone Marrow Research
ISSN : 2578-3351
Launched : 2016
JSM Mathematics and Statistics
ISSN : 2578-3173
Launched : 2014
Journal of Autoimmunity and Research
ISSN : 2573-1173
Launched : 2014
JSM Arthritis
ISSN : 2475-9155
Launched : 2016
JSM Head and Neck Cancer-Cases and Reviews
ISSN : 2573-1610
Launched : 2016
JSM General Surgery Cases and Images
ISSN : 2573-1564
Launched : 2016
JSM Anatomy and Physiology
ISSN : 2573-1262
Launched : 2016
JSM Dental Surgery
ISSN : 2573-1548
Launched : 2016
Annals of Emergency Surgery
ISSN : 2573-1017
Launched : 2016
Annals of Mens Health and Wellness
ISSN : 2641-7707
Launched : 2017
Journal of Preventive Medicine and Health Care
ISSN : 2576-0084
Launched : 2018
Journal of Chronic Diseases and Management
ISSN : 2573-1300
Launched : 2016
Annals of Vaccines and Immunization
ISSN : 2378-9379
Launched : 2014
JSM Heart Surgery Cases and Images
ISSN : 2578-3157
Launched : 2016
Annals of Reproductive Medicine and Treatment
ISSN : 2573-1092
Launched : 2016
JSM Brain Science
ISSN : 2573-1289
Launched : 2016
JSM Biomarkers
ISSN : 2578-3815
Launched : 2014
JSM Biology
ISSN : 2475-9392
Launched : 2016
Archives of Stem Cell and Research
ISSN : 2578-3580
Launched : 2014
Annals of Clinical and Medical Microbiology
ISSN : 2578-3629
Launched : 2014
JSM Pediatric Surgery
ISSN : 2578-3149
Launched : 2017
Journal of Memory Disorder and Rehabilitation
ISSN : 2578-319X
Launched : 2016
JSM Tropical Medicine and Research
ISSN : 2578-3165
Launched : 2016
JSM Head and Face Medicine
ISSN : 2578-3793
Launched : 2016
JSM Cardiothoracic Surgery
ISSN : 2573-1297
Launched : 2016
JSM Bone and Joint Diseases
ISSN : 2578-3351
Launched : 2017
JSM Bioavailability and Bioequivalence
ISSN : 2641-7812
Launched : 2017
JSM Atherosclerosis
ISSN : 2573-1270
Launched : 2016
Journal of Genitourinary Disorders
ISSN : 2641-7790
Launched : 2017
Journal of Fractures and Sprains
ISSN : 2578-3831
Launched : 2016
Journal of Autism and Epilepsy
ISSN : 2641-7774
Launched : 2016
Annals of Marine Biology and Research
ISSN : 2573-105X
Launched : 2014
JSM Health Education & Primary Health Care
ISSN : 2578-3777
Launched : 2016
JSM Communication Disorders
ISSN : 2578-3807
Launched : 2016
Annals of Musculoskeletal Disorders
ISSN : 2578-3599
Launched : 2016
Annals of Virology and Research
ISSN : 2573-1122
Launched : 2014
JSM Renal Medicine
ISSN : 2573-1637
Launched : 2016
Journal of Muscle Health
ISSN : 2578-3823
Launched : 2016
JSM Genetics and Genomics
ISSN : 2334-1823
Launched : 2013
JSM Anxiety and Depression
ISSN : 2475-9139
Launched : 2016
Clinical Journal of Heart Diseases
ISSN : 2641-7766
Launched : 2016
Annals of Medicinal Chemistry and Research
ISSN : 2378-9336
Launched : 2014
JSM Pain and Management
ISSN : 2578-3378
Launched : 2016
JSM Women's Health
ISSN : 2578-3696
Launched : 2016
Clinical Research in HIV or AIDS
ISSN : 2374-0094
Launched : 2013
Journal of Endocrinology, Diabetes and Obesity
ISSN : 2333-6692
Launched : 2013
Journal of Substance Abuse and Alcoholism
ISSN : 2373-9363
Launched : 2013
JSM Neurosurgery and Spine
ISSN : 2373-9479
Launched : 2013
Journal of Liver and Clinical Research
ISSN : 2379-0830
Launched : 2014
Journal of Drug Design and Research
ISSN : 2379-089X
Launched : 2014
JSM Clinical Oncology and Research
ISSN : 2373-938X
Launched : 2013
JSM Bioinformatics, Genomics and Proteomics
ISSN : 2576-1102
Launched : 2014
JSM Chemistry
ISSN : 2334-1831
Launched : 2013
Journal of Trauma and Care
ISSN : 2573-1246
Launched : 2014
JSM Surgical Oncology and Research
ISSN : 2578-3688
Launched : 2016
Annals of Food Processing and Preservation
ISSN : 2573-1033
Launched : 2016
Journal of Radiology and Radiation Therapy
ISSN : 2333-7095
Launched : 2013
JSM Physical Medicine and Rehabilitation
ISSN : 2578-3572
Launched : 2016
Annals of Clinical Pathology
ISSN : 2373-9282
Launched : 2013
Annals of Cardiovascular Diseases
ISSN : 2641-7731
Launched : 2016
Journal of Behavior
ISSN : 2576-0076
Launched : 2016
Annals of Clinical and Experimental Metabolism
ISSN : 2572-2492
Launched : 2016
Clinical Research in Infectious Diseases
ISSN : 2379-0636
Launched : 2013
JSM Microbiology
ISSN : 2333-6455
Launched : 2013
Journal of Urology and Research
ISSN : 2379-951X
Launched : 2014
Journal of Family Medicine and Community Health
ISSN : 2379-0547
Launched : 2013
Annals of Pregnancy and Care
ISSN : 2578-336X
Launched : 2017
JSM Cell and Developmental Biology
ISSN : 2379-061X
Launched : 2013
Annals of Aquaculture and Research
ISSN : 2379-0881
Launched : 2014
Clinical Research in Pulmonology
ISSN : 2333-6625
Launched : 2013
Journal of Immunology and Clinical Research
ISSN : 2333-6714
Launched : 2013
Annals of Forensic Research and Analysis
ISSN : 2378-9476
Launched : 2014
JSM Biochemistry and Molecular Biology
ISSN : 2333-7109
Launched : 2013
Annals of Breast Cancer Research
ISSN : 2641-7685
Launched : 2016
Annals of Gerontology and Geriatric Research
ISSN : 2378-9409
Launched : 2014
Journal of Sleep Medicine and Disorders
ISSN : 2379-0822
Launched : 2014
JSM Burns and Trauma
ISSN : 2475-9406
Launched : 2016
Chemical Engineering and Process Techniques
ISSN : 2333-6633
Launched : 2013
Annals of Clinical Cytology and Pathology
ISSN : 2475-9430
Launched : 2014
JSM Allergy and Asthma
ISSN : 2573-1254
Launched : 2016
Journal of Neurological Disorders and Stroke
ISSN : 2334-2307
Launched : 2013
Annals of Sports Medicine and Research
ISSN : 2379-0571
Launched : 2014
JSM Sexual Medicine
ISSN : 2578-3718
Launched : 2016
Annals of Vascular Medicine and Research
ISSN : 2378-9344
Launched : 2014
JSM Biotechnology and Biomedical Engineering
ISSN : 2333-7117
Launched : 2013
Journal of Hematology and Transfusion
ISSN : 2333-6684
Launched : 2013
JSM Environmental Science and Ecology
ISSN : 2333-7141
Launched : 2013
Journal of Cardiology and Clinical Research
ISSN : 2333-6676
Launched : 2013
JSM Nanotechnology and Nanomedicine
ISSN : 2334-1815
Launched : 2013
Journal of Ear, Nose and Throat Disorders
ISSN : 2475-9473
Launched : 2016
JSM Ophthalmology
ISSN : 2333-6447
Launched : 2013
Journal of Pharmacology and Clinical Toxicology
ISSN : 2333-7079
Launched : 2013
Annals of Psychiatry and Mental Health
ISSN : 2374-0124
Launched : 2013
Medical Journal of Obstetrics and Gynecology
ISSN : 2333-6439
Launched : 2013
Annals of Pediatrics and Child Health
ISSN : 2373-9312
Launched : 2013
JSM Clinical Pharmaceutics
ISSN : 2379-9498
Launched : 2014
JSM Foot and Ankle
ISSN : 2475-9112
Launched : 2016
JSM Alzheimer's Disease and Related Dementia
ISSN : 2378-9565
Launched : 2014
Journal of Addiction Medicine and Therapy
ISSN : 2333-665X
Launched : 2013
Journal of Veterinary Medicine and Research
ISSN : 2378-931X
Launched : 2013
Annals of Public Health and Research
ISSN : 2378-9328
Launched : 2014
Annals of Orthopedics and Rheumatology
ISSN : 2373-9290
Launched : 2013
Journal of Clinical Nephrology and Research
ISSN : 2379-0652
Launched : 2014
Annals of Community Medicine and Practice
ISSN : 2475-9465
Launched : 2014
Annals of Biometrics and Biostatistics
ISSN : 2374-0116
Launched : 2013
JSM Clinical Case Reports
ISSN : 2373-9819
Launched : 2013
Journal of Cancer Biology and Research
ISSN : 2373-9436
Launched : 2013
Journal of Surgery and Transplantation Science
ISSN : 2379-0911
Launched : 2013
Journal of Dermatology and Clinical Research
ISSN : 2373-9371
Launched : 2013
JSM Gastroenterology and Hepatology
ISSN : 2373-9487
Launched : 2013
Annals of Nursing and Practice
ISSN : 2379-9501
Launched : 2014
JSM Dentistry
ISSN : 2333-7133
Launched : 2013
Author Information X