From the Editor
......................................................................................................................................................................
Ahmad Husari
Editor, Middle-East
Journal of Internal Medicine
Director, American University of Beirut Sleep
Disorders Center
Director, American University of Beirut outpatient
clinical care services
Assistant Professor
Division of Pulmonary and Critical Care Medicine
American University of Beirut Medical Center
Beirut Lebanon
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This is
the first issue this year of the journal that
has a number of interesting papers dealing with
various subjects of interest. There are three
papers that dealt with Sickle Cell Disease.
Mustafa et al., looked at improving
the outcome of Sickle Cell disease patients in
a resource limited setting Sudan Sickle Cell Anemia
Center (SSCAC). They stressed that it is a promising
and developing experience. In 2010, the percentage
of newborns with SCD in sub-Saharan Africa was
79%, and this proportion is expected to increase
to 88% by 2050. Africa has high mortality rates
ranging from 50 to 90% for those aged less than
5 years. This high mortality is due to the lack
of several facilities like prenatal diagnostic
services, systematic follow-up, and life-saving
measures such as penicillin prophylaxis, vaccination
for common bacterial diseases, and the provision
of disease-modifying treatment with Hydroxyurea,
and Poor access to hematopoietic stem cell transplantation.
Infectious diseases like malaria may also play
a role in increasing the severity and mortality.
The prevalence rate of sickle cell anemia in Sudan
ranging from 2 to 30.4%. The highest prevalence
of SCA in the Sudanese population is found in
Western Sudan residents. Because of this increased
prevalence of SCD in west Sudan, it is of high
importance to improve the quality of care for
sickle cell disease patients in this area. The
authors present their experience at SSCAC.
Helvaci*, et al., tried to understand
the underlying mechanism of pulmonary hypertension
(PHT) in the sickle cell diseases (SCD). All patients
with the SCD were included. The study included
434 patients (212 females) with similar mean ages
in males and females (30.8 versus 30.3 years,
respectively, p>0.05). Smoking (23.8% versus
6.1%, p<0.001) and alcohol (4.9% versus 0.4%,
p<0.001) were higher in males, significantly.
Transfused units of red blood cells (RBC) in their
lives (48.1 versus 28.5, p=0.000), disseminated
teeth losses (<20 teeth present) (5.4% versus
1.4%, p<0.001), chronic obstructive pulmonary
disease (COPD) (25.2% versus 7.0%, p<0.001),
ileus (7.2% versus 1.4%, p<0.001), cirrhosis
(8.1% versus 1.8%, p<0.001), leg ulcers (19.8%
versus 7.0%, p<0.001), digital clubbing (14.8%
versus 6.6%, p<0.001), coronary heart disease
(CHD) (18.0% versus 13.2%, p<0.05), chronic
renal disease (CRD) (9.9% versus 6.1%, p<0.05),
and stroke (12.1% versus 7.5%, p<0.05) were
all higher but not PHT (12.6% versus 11.7%, p>0.05)
in males, significantly. The authors concluded
that SCD are severe inflammatory processes on
vascular endothelium, particularly at the capillary
level since the capillary system is the main distributor
of hardened RBC into the tissues. Although the
higher smoking, alcohol, and disseminated teeth
losses, COPD, ileus, cirrhosis, leg ulcers, digital
clubbing, CHD, CRD, and stroke-like atherosclerotic
consequences in male sex, PHT was not higher in
them in the present study. In another definition,
PHT may not have an atherosclerotic background
in the SCD. Instead, the hardened RBC-induced
capillary endothelial damage, inflammation, edema,
and fibrosis around the alveoli may be the major
underlying cause.
Helvaci*, et al., tried to understand
prevalence of chronic obstructive pulmonary disease
(COPD) in both genders in sickle cell diseases
(SCD).All cases with the SCD in the absence of
smoking and alcohol were included. The study included
368 patients (168 males). Mean ages were similar
in males and females (29.4 versus 30.2 years,
respectively, p>0.05). Mean values of body
mass index (BMI) were similar in males and females,
too (21.7 versus 21.6 kg/m2, respectively, p>0.05).
Interestingly, total bilirubin value of the plasma
(5.2 versus 4.0 mg/dL, p=0.011), transfused units
of red blood cells (RBC) in their lives (46.8
versus 29.2, p=0.002), COPD (20.8% versus 6.0%,
p<0.001), and digital clubbing (13.0% versus
5.5%, p<0.001) were all higher in males. Whereas
painful crises per year (5.0 versus 5.0), pulmonary
hypertension (10.1% versus 12.5%), acute chest
syndrome (2.3% versus 3.5%), mortality (8.3% versus
6.5%), and mean age of mortality (29.0 versus
32.5 years) were similar in males and females,
respectively (p>0.05 for all). The authors
concluded that SCD are severe inflammatory processes
on vascular endothelium particularly at the capillary
level, since capillary system is the main distributor
of hardened RBC into tissues. The capillary endothelial
damage, inflammation, edema, and fibrosis induced
hypoxia may be the underlying cause of COPD in
the SCD. Although the similar BMI and absence
of smoking and alcohol, the much higher prevalence
of COPD may be explained by the dominant role
of male sex in life according to the physical
power that may accelerate systemic atherosclerotic
process in whole body.
Abyad & Hammami in the first
of a series on Frailty discusses frailty. They
stressed Life expectancy continues to rise globally.
However, the additional years of life do not always
correspond to years of healthy life, which may
result in an increase in frailty. Given the rapid
aging of the population, the association between
frailty and age, and the impact of frailty on
adverse outcomes for older adults, frailty is
increasingly recognized as a significant public
health concern. Early detection of the condition
is critical for assisting older adults in regaining
function and avoiding the negative consequences
associated with the syndrome. Despite the critical
nature of frailty diagnosis, there is no conclusive
evidence or consensus regarding whether routine
screening should be implemented. A variety of
screening and assessment instruments have been
developed from a biopsychosocial perspective,
with frailty defined as a dynamic state caused
by deficits in any of the physical, psychological,
or social domains associated with health. All
of these aspects of frailty should be identified
and addressed through the use of a comprehensive
and integrated approach to care. To accomplish
this goal, public health and primary health care
(PHC) must serve as the fulcrum around which care
is delivered, not just to the elderly and frail,
but to all individuals, by emphasizing a life-course
and patient-centered approach centered on integrated,
community-based care. Personnel in public health
should be trained to address frailty not just
clinically, but also in a societal context. Interventions
should take place in the context of the individuals'
environment and social networks. Additionally,
public health professionals should contribute
to community-based frailty education and training,
promoting community-based interventions that assist
older adults and their caregivers in preventing
and managing frailty. The purpose of this paper
is to provide an overview of frailty for a public
health audience in order to increase awareness
of the multidimensional nature of frailty and
how it should be addressed through an integrated
and holistic approach to care.
Questioning and prying into botulinum
toxin after aesthetic treatment
Dr. Elghblawi reported
a case of an allergy to Botox toxin A. that had
arisen shortly after the injection, to be added
to the existing literature. A 41-year-old Philippino
lady experienced a severe localised reaction,
with redness and nodular swelling on her face,
after her second Botox injection. The lady did
not have any prior medical illness. This case
can help in assessment and appraisal of anticipated
Botox allergies and raise awareness of the rare
infrequent incident.
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