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International Journal of Clinical Anesthesiology

Clinical Correlates to One Year Mortality Following Tracheostomy of Adult Intensive Care Patients

Research Article | Open Access

  • 1. Department of Anesthesiology, Department of Pulmonary and Critical Care Medicine, and
  • 2. Department of Otolaryngology, Pennsylvania State University College of Medicine, USA
  • 3. Department of Otolaryngology, Thomas Jefferson University, USA
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Corresponding Authors
Sonia Vaida, Department of Anesthesiology, Penn State and Milton S. Hershey Medical Center, 500 University Drive, P.O. Box 850, Mailcode H187, Hershey, Pennsylvania, 17033, USA, Tel: 717-531-8433
Abstract

Background: Tracheostomy is a common surgical procedure performed in the adult intensive care unit (ICU) population etc. Our objective was to identify characteristics associated with one year mortality in adult ICU patients following tracheostomy placement.

Methods: A retrospective chart review was conducted on adult ICU patients admitted at Penn State Hershey Medical Center between January 2004 and December 2009 (n=193) who had a first time tracheostomy. Using univariate statistical analysis with logistic regression and Bonferonni correction, the significance of individual characteristics to one year mortality following tracheostomy was determined. Statistical significance was considered p< 0.05; all p values reported are Bonferonni-corrected values.

Results: Mortality at one year following tracheostomy was 21.2% (41 of 193 patients). A total of nine variables were found to have a statistically significant correlation with patient mortality: one week increase in continuous intravenous sedation length following tracheostomy (p=0.00057), fourteen day increase in total mechanical ventilation length (p=0.00082), hyperglycemia (p=0.00130), continuous intravenous vasopressor medication infusions during tracheostomy (p=0.00222), acute renal failure (p=0.00471), increased age (p=0.00892), continuous intravenous vasopressor medication infusions during ICU stay (p=0.01711), hemodialysis (p=0.02813), and a 10,000 cell/μL increase in peak white blood cell count (p=0.03574).

Conclusions: Clinical factors associated with increased mortality of adult ICU patients one year following tracheostomy were identified. These factors may indicate greater severity of systemic dysfunction in an already critically ill population leading to increased mortality

Citation

Grap SM, Goldenberg M, Huntley C, High K, Wojnar MM, et al. (2014) Clinical Correlates to One Year Mortality Following Tracheostomy of Adult Intensive Care Patients. Int J Clin Anesthesiol 2(4): 1039.

INTRODUCTION

Tracheostomy is a common procedure performed on adult patients in the Intensive Care Unit (ICU) setting and is performed in approximately 10% to 12% of patients requiring mechanical ventilation for >24 hours [1,2]. Patients requiring tracheostomy have a higher hospital survival rate than patients ventilated via endotracheal tube alone [3]. However, tracheostomy is not without associated mortality. A 20% mortality of tracheostomy patients was found at 28 days following the initiation of mechanical ventilation [4]. The reported mortality rate in patients one year following tracheostomy is 36% [5]. Shah et al. [6] have reported a 19.2% national in-hospital mortality of patients receiving tracheostomy.Identified risk factors of inhospital mortality following tracheostomy include: hospital region, non-teaching centers, increased age, and co-existing cardiac conditions [7].

We investigated clinical factors associated with one year mortality in adult ICU patients following tracheostomy. Our primary outcome was mortality at one year following tracheostomy. We sought to identify individual patient characteristics as clinical factors of mortalityafter tracheostomy in adult ICU patients.

MATERIALS AND METHODS

A retrospective chart review of adult ICU patients having undergone a tracheostomy was conducted. Approval was obtained from the Penn State College of Medicine Institutional Review Board. The need for informed consent was waived due to the retrospective study design. Potential subjects included adult patients admitted to the Penn State Hershey Medical Center ICU between January 1, 2004 to December 31, 2009, who had a tracheostomy procedure during the ICU stay. Patients included in the study were ≥18 years of age and did not have a previous tracheostomy prior to admission. Patients who underwent a tracheostomy in addition to surgical procedure were also included in the study. A total of 247 patient charts were reviewed and included in the collection of patient characteristic data.

Data for categorical and continuous patient characteristics were collected during chart review. Data related to patient characteristics included patient sex, race, and age on ICU admission. Other patient variables specific to ICU admission included: body mass index, traumatic motor vehicle accident, traumatic injury excluding motor vehicle accident, respiratory status (spontaneous ventilation, mechanical ventilation, or respiratory distress requiring intubation without mechanical ventilation), Glasgow Coma Scale score, and the adult ICU location (surgical, medical, neuroscience, or heart and vascular units). Surgical procedures, other than tracheostomy, that were performed during hospitalization were included as variables according to specialty (general/colorectal, orthopedic, neurosurgery, otolaryngology for tumor resection, otolaryngology for traumatic injury, vascular, cardiac, and noncardiacintrathoracic.) A tracheostomy performed in conjunction with another surgical procedure was included as a separate individual variable.

Hyperglycemia was defined as two or more consecutive blood glucose measurements>200 mg/dL, during the hospitalization, independent of insulin administration. Acute renal failure during the ICU stay was defined as a creatinine level >2.0 mg/dL or an increase in creatinine >1.0 mg/dL abovebaseline in chronic kidney disease. Hemodialysis during the ICU admission included both intermittent sessions and continuous renal replacement therapy.

The use of vasopressor medication infusions during both the ICU stay and tracheostomy procedure included the continuous administration of one or more of the following intravenous medications: phenylephrine, norepinephrine, dopamine, dobutamine, and epinephrine. Transfusion of blood products included one or more of the following: packed red blood cells, fresh frozen plasma, or pooled donor platelets. The presence of infection was identified by positive culture result, and included respiratory, urinary, and blood samples. Variables specific to the ICU stay included: nadir white blood cell (WBC) count, peak WBC count, admission hemoglobin level, nadir hemoglobin level, nadir platelet count, peak prothrombin time, peak partial prothrombin time, peak international normalized ratio, lowest Glasgow Coma Scale score, and total length of endotracheal intubation prior to tracheostomy. Also included were: the number of days of weaning attempts to endotracheal extubation, wean to extubation failures requiring reintubation, sedation days prior to tracheostomy, sedation days following tracheostomy, length of mechanical ventilation, and length of ICU stay.

Variables specific to the tracheostomy procedure included: the hospitalization day of tracheostomy placement, surgical service performing tracheostomy, percutaneous or surgical tracheostomy, procedure location (in operating room or ICU bedside), WBC count on procedure day, hemoglobin 14 seconds, partial prothrombin time >40 seconds, or international normalized ratio >1.2.

The administration of total parenteral nutrition (TPN), provision of enteral feeding, and ability to ambulate at any time during the hospitalization were included as variables. Hospital discharge characteristics included: the hospitalization length, respiratory support status (decannulated, liberated from mechanical ventilation on room air, tracheostomy collar, continuous positive airway pressure, or synchronous intermittent mechanical ventilation). The patient discharge location was included (rehabilitation hospital, long term acute care hospital, skilled nursing facility, other university or community hospital, hospice, or home).

Statistical analysis

The primary intent was to determine if there is an association between the collected patient characteristics and mortality within one year following tracheostomy placement. A total of 59 patients were excluded from the analysis due to missing follow up status or unknown disposition at one year following tracheostomy. The final analysis included 193 patients. Univariate statistical analysis was conducted for both categorical and continuous patient variables using logistic regression models for the outcome of death at one year. For continuous factors, a linear relationship was assumed between the factor and the outcome. This relationship was checked and verified using methods. Only ICU nadir platelet count showed a significant non-linear trend; therefore a quadratic effect, as suggested by the curvefitting methods, was used for this variable. Odds ratios (OR) and Bonferroni-corrected 95% confidence intervals (CI) for all variables are reported. We assessed 43 variables in total and used the Bonferonni correction to hold the overall type error rate at 5%. Thus, we multiplied eachuncorrected p-value by 43 to obtain the Bonferonni-corrected p-value which is reported. Bonferonni corrected p-values <0.05 were considered significant.SAS system 9.3 software was used to conduct the statistical analysis.

RESULTS

We found a mortality rate of 21.2% (41 out of 193 patients) at one year following tracheostomy.The data for categorical (Tables 1 & 2) and continuous variables (Table 3) are detailed in Tables 1-3.We identified nine patient variables as significantly associated with one year mortality following tracheostomy (p<0.05). Table 4 contains the results from the statistical analysis of all 43 variables tested.Estimated odds ratios for logistic regression of each variable modeled separately, as well as Bonferonni-corrected 95% confidence intervals and p-values are shown.

Of the variables that significantly correlated with one year mortality following tracheostomy, five demonstrated ORs >4: hemodialysis (OR=5.8), hyperglycemia, continuous vasopressor infusion(s), and vasopressor infusion during the tracheostomy procedure (OR=5.0 for each), and acute renal failure (OR=4.2). The remaining significantly associated variables exhibited ORs between 1.7 and 2.1: age (OR=2.2), a peak WBC count increased by10,000 cells/µL (OR=2.1), total mechanical ventilation increased by 14 days (OR=2.0), and an increase of 1 week for sedation days post-tracheostomy (OR=1.7).

Table 1: Data for categorical and continuous variables before Surgery.

Characteristic Variable Overall N Number Percent age
Sex 193    
Male   133 68.9
Female   60 31.1
       
Race 193    
Caucasian   180 93.3
Hispanic   6 3.1
African American   5 2.6
Asian   1 0.5
Other   1 0.5
       
Admission Respiratory Status 192    
Spontaneous Ventilation   147 76.6
Intubated   44 22.9
Respiratory Distress   1 0.5
       
Admitting ICU 193    
Surgical   183 94.8
Medical   6 3.1
Neuroscience   3 1.6
Heart and Vascular   1 0.5
       
Lowest GCS Score 189    
15   30 15.8
3 (or 3T)   159 83.7
       
Surgical Service Performing Tracheostomy 191    
Emergency General Surgery   113 59.2
Otolaryngology   73 38.2
Other   5 2.6
       
Tracheostomy Type 191    
Open   144 75.4
Percutaneous   47 24.6
       
Tracheostomy Procedure Location 191 144 75.4
Operating Room   47 24.6
Bedside      
       
Respiratory Status on Discharge 174    
Spontaneous Ventilation on Room Air   70 36.3
Tracheostomy Collar   46 23.8
Decannulated   44 22.8
Synchronous Intermittent Mechanical Ventilation   8 4.1
Continuous Positive Airway Pressure   6 3.1
       
Location to Discharge 172    
Rehabilitation Facility   57 29.7
Home   54 28.1
Long Term Acute Care Hospital   48 25.0
Skilled Nursing Facility/Nursing Home   9 4.7
Other University/Community Hospital   4 2.1

Table 2: Data for categorical and continuous variables after Surgery.

Characteristic Variable Overall N Yes No
    N % N %
Admitting Diagnosis - Traumatic Motor Vehicle Accident 193 62 32.1 131 67.9
Admitting Diagnosis - Non Motor Vehicle Accident Traumatic Injury 193 88 45.6 105 54.4
General/Colorectal Surgery Performed 167 56 33.5 111 66.5
Orthopedic Surgery Performed 167 32 19.2 135 80.8
Otolaryngology Surgery (Tumor) Performed 167 38 22.8 129 77.2
Otolaryngology Surgery (Traumatic) Performed 167 18 10.8 149 89.2
Neurosurgery Performed 167 23 13.8 144 86.2
Vascular Surgery Performed 167 11 6.6 156 93.4
Intrathoracic Non-Cardiac Surgery Performed 167 7 4.2 160 95.8
Cardiac Surgery Performed 167 5 3.0 162 97.0
Acute Renal Failure 192 51 26.6 141 73.4
Vasopressor Medication Infusion(s) 185 49 26.5 136 73.5
Hyperglycemia 191 78 40.8 113 59.2
Infection (positive culture) 187 116 62.0 71 38.0
Blood Product Transfusion 181 83 45.9 98 54.1
TPN Administration 193 52 26.9 141 73.1
Enteral Feeding 193 161 83.4 32 16.6
Hemoglobin <8 g/dL on Procedure Day 178 12 6.7 166 93.3
Coagulopathy on Procedure Day 183 74 40.4 109 59.6
Procedural Antibiotics Administered 190 151 79.5 39 20.5
Vasopressor Infusion(s) During Procedure 188 38 20.2 150 79.8
Surgical Procedure Involving Tracheostomy 193 51 26.4 142 73.6

 

DISCUSSION

We found a one year mortality of 21.2% following tracheostomy in adult ICU patients. This is consistent with previous reports [3-6]. Esteban, et al. [4], demonstrated a one year mortality of 36% following hospital discharge and a 28 day mortality of 20% in patients who underwent a tracheostomy.4 A prospective cohort study of patients receiving mechanical ventilation found a lower overall hospital mortality in patients with a tracheostomy (13.7% mortality) in comparison to those ventilated with an endotracheal tube (26.4% mortality) [3]. findings show that an of one week of continuous intravenous sedation following tracheostomy placement results in higher one year mortality. Deep sedation has been previously correlated with higher ICU mortality within 28 days and increased mortality at six months following ICU discharge [7]. Spontaneous awakening and breathing trials have also been shown to improve overall one year survival in ICU patients, suggesting that decreased sedation time may be beneficial [8].Interestingly, the number of sedation days prior to tracheostomy was not found to be significant to mortality in our study. This may suggest that patients requiring prolonged deep levels of sedation post-tracheostomy have more comorbidities than those patients who do not, thus leading to increased mortality.

We found that a 14 day increase of total mechanical ventilation, with either an endotracheal tube or tracheostomy, was a predictor of one year mortality following tracheostomy (OR=2.0). Previous studies also suggest that mechanical ventilation for an extended period of several weeks is associated with increased patient mortality [9]. However, we did not find that the length of mechanical ventilation with an endotracheal tube prior to tracheostomy was a significant factor of mortality. Consistent with previous reports, we did not find a significant correlation between hospital or ICU patient mortality and timing of tracheostomy placement [10,11].

In this study, hyperglycemia during the ICU stay was found to be a significant risk factor for one year mortality following tracheostomy (OR=5.0). Previous studies have suggested that hyperglycemia is positively associated with poor ICU outcomes [12-15]. ICU patients have an increased risk of developing hyperglycemia, especially with elevated baseline blood glucose levels in both diabetic and non-diabetic patients [16]. Hyperglycemia is correlated with increased organ dysfunction, suggesting detrimental systemic effects leading to increased mortality [15].

Use of vasopressor medication infusions, both during the ICU stay and tracheostomy procedure, was independently associated with one year mortality following tracheostomy in our study. Vasopressor medication use during mechanical ventilation has previously been associated with patient mortality [4]. Shah et al. [6], have reported a higher in-hospital mortality of tracheotomy patients with cardiac conditions, including myocardial infarction, congestive heart failure, and cardiomyopathy.This supports our finding of increased mortality with vasopressor usage during tracheostomy procedure and ICU stay, since the use of vasopressor medication infusions is often due to acute cardiovascular collapse and instability.

We found acute renal failure to be a clinical risk factor of one year mortality following tracheostomy (OR=4.2). Acute renal failure was previously found to be a risk factor for increased ICU patient mortality [14-17]. Previous studies have shown that renal dysfunction is more prevalent in elderly patients requiring mechanical ventilation [5] and elderly tracheostomy patients [18]. New onset renal dysfunction was found to be the most prevalent risk factor for mortality in patients having tracheostomy for respiratory failure [5]. Additionally, we found that hemodialysis during the ICU stay conferred a 5.8 times increased risk of mortality at one year following tracheostomy. Previous research has found a higher mortality among ICU patients requiring hemodialysis for the development of acute renal failure and acute kidney injury, suggesting an increased severity of disease [19,20].

Increased age has been shown to be a significant risk factor for mortality in patients with either mechanical ventilation or tracheostomy [2,4–6,9,18]. Several previous studies have been limited to elderly age groups ≥65 years [5,18]. Our study included ICU patients 18 years of age or older and we also found that increased age (defined as) is a significant risk factor for mortality at one year following tracheostomy. Other studies have found increased age as a risk factor for mortality during mechanical ventilation [4,9] and during a hospital stay during which tracheostomy is performed [6]. Lowest survival rates for patients requiring mechanical ventilation have been reported for patients age >70 years [2]. Previous postulates for increased mortality among the elderly were the presence of more comorbidities and traumatic injuries in comparison to a younger population [18]. However, in our study, the presence of traumatic injuries was not a significant factor for one year mortality following tracheostomy.

A 10,000 cell/µL increase in WBC count during the ICU stay was found to significantly correlate with higher mortality at one year following tracheostomy. Previous authors have shown that the presence of infection in adult ICU patients is a significant risk factor for both increased ICU mortality and overall hospital mortality [21]. Increased ICU mortality has been associated with both leukopenic and exaggerated leukemoid responses (WBC count >25,000cells/µL) [22]. Interestingly, in our study, the presence of infection determined by positive respiratory, urinary, and/or blood cultures was not significant to mortality. This may be due to severe disease marked by a leukemoid response independent of the presence of infection, in which cultures may not have been obtained. We propose that patients with higher peak WBC counts may have more systemic illness causing increased mortality risk.

We have identified several clinical factors associated with one year mortality following tracheostomy in adult ICU patients. These factors may independently represent increased disease severity in an already critically ill patient population. This may contribute to increased mortality in these patients following tracheostomy. Although we have identified these clinical factors in association to mortality following tracheostomy, several of these factors have also been individually correlated to increased ICU patient mortality [14,16,17]. Perhaps the individual factors we have found to be associated with one year mortality following tracheostomy are markers for systemic organ dysfunction and disease severity leading to patient mortality.

We included all adult ICU patients receiving a first time tracheostomy, whereas previous studies have been limited to only those patients with respiratory failure [5,4]or elderly populations [2,18]. We aimed to include all adult age groups in order to have a patient demographicrepresentative of that found across both surgical and medical ICUs.

A limitation to this study is the retrospective design of the chart review. Although we have identified multiple clinical factors with significant association to one year mortality following tracheostomy, the retrospective design makes it difficult to distinguish if the associations are a direct cause or markers for mortality. Further studies will be necessary to clarify this issue. risk factors associated with post-tracheostomy related mortality may contribute to increased patient safety.

Table 3 Data for Characteristic Variable.

Characteristic Variable Overall N Mean (SD) Median Range
Age at admission (years) 193 51 (19) 52 18-97
Admitting Body Mass Index (kg/ m2 ) 170 28.9 (9.0) 27 14-67
Admitting GCS Score 191 11.8 (5.0) 15 3.0-15.0
Peak WBC Count (thousands of cells/µL) 185 21.1 (9.1) 19.2 7.0-83.9
Nadir WBC Count (thousands of cells /µL) 185 7.7 (3.3 0 7.1 0.2-22.3
Nadir Hemoglobin (g/dL) 185 8.2 (1.8) 7.8 3.9-14.7
ICU Admission Hemoglobin (g/ dL) 184 11.8 (2.2) 11.6 5.4-17.4
Nadir Platelet (thousands of cells /µL) 185 120.1 (64.8) 114.0 7.0- 319.0
Peak Prothrombin Time (seconds) 153 17.9 (11.6) 13.4 10.4- 79.5
Peak International Normalized Ratio 153 1.8 (1.4) 1.3 1.0-13.2
Peak Partial Thromboplastin Time (seconds) 149 59.3 (39.4) 41.0 2.3- 150.0
Hospitalization Day of Tracheostomy 193 9.5 (9.3) 7.0 1.0-60.0
Pre-Tracheostomy Sedation Days 189 7.4 (7.0) 6.0 0.0-28.0
Post-Tracheostomy Sedation Days 180 9.1 (13.8) 4.0 0.0-86.0
Wean Attempts Pre Tracheostomy 184 1.4 (1.1) 1.0 0.0-5.0
Wean to Extubation Failures Pre-Tracheostomy 184 0.6 (0.9) 0.0 0.0-4.0
Total Mechanical Ventilation Days 180 16.0 (17.5) 12.0 0.0- 101.0
Total Days of Intubation Pre Tracheostomy 190 7.2 (7.0) 6.0 0.0-28.0
Total ICU Days 134 31.3 (26.4) 25.0 4.0- 207.0
Total Hospitalization Days 174 31.3 (26.4) 25.0 4.0- 207.0

Table 4: Results of Statistical Analysis of Patient Variables in Association with One Year Mortality Following Tracheostomy

Characteristic Variable OR 95% CI* p-value*
ICU Admission variables      
Age 2.16 1.10-4.23 0.00892
Sex 0.48 0.15-1.59 1.0000
BMI 0.82 0.39-1.72 1.0000
Spontaneous ventilation 1.28 0.31-5.35 1.0000
GCS Score, Increase of 1 1.00 0.89-1.12 1.0000
Hemoglobin level, increase of 1g/dL 0.86 0.67-1.12 1.0000
Diagnosis of trauma (non-MVA) 0.48 0.14-1.60 1.0000
Diagnosis of traumatic MVA 0.44 0.11-1.77 1.0000
Surgical Procedure(s) During Hospitalization (Other than tracheostomy)
Otolaryngology for tumor resection 0.40 0.06-2.58 1.0000
Otolaryngology for traumatic injury 0.22 0.01-6.49 1.0000
Orthopedic 0.52 0.08-3.37 1.0000
Neurosurgery 1.52 0.28-8.31 1.0000
General surgery/colorectal 1.38 0.37-5.07 1.0000
Hospitalization Stay Variables      
Hyperglycemia 4.98 1.43-17.4 0.00130
TPN administration 2.36 0.71-7.91 0.86612
Enteral feeding 1.20 0.24-5.95 1.00000
Hospitalization day of ambulation, increase of 1 day 0.96 0.90-1.05 1.00000
ICU Stay Variables      
Sedation days pre-tracheostomy; increase of 1 week 1.46 0.84-2.53 1.00000
Sedation days post-tracheostomy; increase of 1 week 1.66 1.14-2.41 0.00057
Total mechanical ventilation days;increase of 14 days 2.02 1.19-3.47 0.00082
Number of wean attempts, increase of 1 day 1.14 0.69-1.91 1.00000
Number of wean to extubation failures; increase of 1 day 1.54 0.86-2.73 0.69485
Acute renal failure 4.24 1.26-14.2 0.00471
Continuous vasopressor infusion(s) 4.96 1.37-18.0 0.00222
Hemodialysis 5.76 1.08-30.7 0.02813
Infection (positive culture results) 2.52 0.65-9.64 1.00000
Peak WBC count; increase of 10,000 cells/µL 2.08 1.02-4.26 0.03574
Nadir WBC count; increase of 1 K/µL 1.00 0.83-1.19 1.00000
Peak PT;increase of 10 seconds 1.46 0.90-2.40 0.48471
Peak INR; increase of 1 1.42 0.89-2.29 0.61134
Peak PTT; increase of 50 seconds 1.50 0.71-3.12 1.00000
Nadir platelet count; 68 vs. 157 (quadratic trend) 1.86 0.73-4.76 1.00000
Nadir hemoglobin level; increase of 1 g/dL 0.80 0.55-1.19 1.00000
Blood product transfusion 0.76 0.23-2.57 1.00000
Lowest GCS Score; 3 (or 3T) vs. 15 2.84 0.36-22.4 1.00000
Tracheostomy Procedure Variables      
Hospitalization day of tracheostomy; increase of 1 day 1.06 0.99-1.12 0.18239
Tracheostomy combined with other surgical procedure 0.58 0.22-1.55 1.00000
Percutaneous tracheostomy (vs. open) 1.42 0.39-5.13 1.00000
Surgical antibiotics prior to tracheostomy 2.12 0.40-11.4 1.00000
Vasopressor infusions during tracheostomy 4.96 1.37-18.0 0.00222
Coagulopathy on day of tracheostomy 1.44 0.45-4.67 1.00000
WBC count on day of tracheostomy; ≥10,000 cells/µL vs. <10,000 cells/µL 1.76 0.47-6.61 1.00000
Emergency general surgery service performing tracheostomy (vs. Otolaryngology and other) 1.82 0.52-6.27 1.00000
*Estimated odds ratios (OR) for logistic regression for each variable 
modeled separately. Bonferonni-corrected 95% confidence intervals 
(CI) and p-values are shown. Abbreviations: ICU=Intensive Care 
Unit, BMI=Body Mass Index, GCS=Glasgow Coma Scale, MVA=Motor 
Vehicle Accident, TPN=Total Parenteral Nutrition, WBC=White Blood 
Cell, PT=Prothrombin Time, INR=International Normalized Ratio, 
PTT=Partial Thromboplastin Time.

 

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Received : 09 Aug 2014
Accepted : 01 Nov 2014
Published : 03 Nov 2014
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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
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