Month: May 2024

Acute Conditions

Asthma Asthma is a disease that is characterised by reversible bronchoconstriction, bronchial hyper-responsiveness, and airway inflammation. Allergens induce a Th2 response which stimulates production of IgE and attracts eosinophils to the airways, leading to airway inflammation. This leads to the release of chemical mediators (such as histamine and leukotrienes) which leads to bronchoconstriction increasing airway resistance.   Risk factors Personal or family history of atopic conditions (allergic rhinitis, eczema) Air pollution Precipitants – cold air, allergens (ask about pets, carpet etc.) Drugs – e.g., aspirin intolerant asthma (usually features nasal polyps) Occupational (baking, factory work) – this classically causes reduced peak

Hypersensitivity

The airways are also prone to being affected by hypersensitivity reactions – these are abnormal immune responses to normal stimuli. These are categorised into 4 different types.   Type 1 This is a rapid allergic reaction due to pre-formed IgE antibody to an exposed antigen. – It eventually leads to a large increase in histamine which can lead to anaphylactic shock.   Histamine is stored in mast cells and is released by calcium-dependent exocytosis: – IgE binds IgE receptor –> increases intracellular IP3 –> increases Calcium – Intracellular cAMP is an antagonist and works to block release of histamine Histamine

Oxygen and CO2

At the lungs, alveolar ventilation is matched with pulmonary blood flow to create a concentration gradient to exchange O2 and CO2 – Oxygen binds to haemoglobin and is transported in the blood. – The dissociation curve is sigmoidal, due to the cooperative binding of oxygen molecules. – This means that it is at first difficult to load the first oxygen molecule onto haemoglobin – However, once the first one binds, this causes a conformational shift which increases haemoglobin’s affinity for oxygen   It is then easier to bind the next oxygen molecules. This causes the steep rise in the oxygen dissociation

Lung Volume and Compliance

We can use spirometry to measure some key volumes of the lungs: Tidal volume = volume of air breathed in and out of the lungs during quiet breathing (500ml)   Inspiratory reserve volume = the maximal volume that can be inhaled from the end-inspiratory level   Expiratory reserve volume = describes the maximal volume of air that can be further exhaled subsequent to the volume achieved at the end of the exhalation phase of quiet breathing   Residual volume (RV) = the volume of air left in the lungs following expiration of the expiratory reserve volume i.e. the maximal exhalation capacity   Inspiratory capacity =

Breathing and Ventilation

The breathing system relies on creating a pressure gradient between the inside and external environment, which needs an intimate relationship between the lungs and chest wall. – Lungs are lined by visceral and parietal pleura, which are separated by a thin layer of fluid.   The volume of thoracic cavity is determined by the outward recoil of chest wall + inward elastic recoil of lungs – These opposing forces are balanced by small negative pleural pressure. Breathing relies on increasing thoracic cage volume which then decreases intrapleural pressure i) At the end of expiration, alveolar pressure (PA) = 0 and

Anatomy of the Thorax

The thorax is divided by a transverse plane at the angle of Louis (T4/5) into the superior and inferior mediastinum. The latter can be subdivided into the anterior, middle and posterior compartments.   Ribs There are a total of 12 ribs: – Ribs 1 to 7 attached to sternum by costal cartilage – “true ribs” – Ribs 8 to 10 attached to the rib above by costal cartilage – “false ribs” – Ribs 11 and 12 are so-called “floating ribs,” as do not articulate with the sternum anteriorly   Airways The airway starts with the trachea which begins, beneath the

Sleep Apnoea

Obstructive Sleep Apnoea This is a condition where the walls of the airway briefly collapse during sleep. This obstructs the airway causing cessation of breathing during sleep (apnoea) followed by partial arousal to regain breath. The patient then falls asleep again and the cycle repeats itself. It can lead to pulmonary hypertension and type II respiratory failure. It is classically seen in middle-aged obese men who complain of loud snoring.   Risk factors Obesity Large tonsils Large tongue (macroglossia) Symptoms Loud snoring Lethargy with daytime napping Morning headache Decreased libido Hypertension Compensated respiratory acidosis   Key tests Epworth sleepiness scale

Acute Conditions

Acute Respiratory Distress Syndrome (ARDS) This refers to widespread inflammation at the alveolar-capillary interface, increasing the permeability of the alveolar capillaries. Fluid moves out of the permeable capillaries, resulting in non-cardiogenic pulmonary oedema that impairs ventilation. ARDS can progress to organ failure and carries a high morbidity and mortality risk. Causes Direct – this is due to direct lung injury (such as smoke inhalation) Indirect – due to conditions which cause inflammation (such as sepsis, shock and acute pancreatitis)   Symptoms Acute onset tachypnoea, dyspnoea Bilateral inspiratory crackles Low oxygen saturations and cyanosis with respiratory distress   Key tests ABG

Lung Cancer

This is a broad term which is most common cancer in the UK, which typically occurs in people of 60 years. It can be broken down into several types of specific types of cancers, which have different histology. Metastases are more common, typically arising from breast, prostate, colon, kidney and uterus. NICE Referral Guidelines   Carcinoma of the bronchus This type of carcinoma is generally divided into 2 main categories:   Small Cell Carcinoma This is a tumour which arises from neuro-endocrine cells in the lungs. It is named “small cell” because the cancerous cells look small when viewed under

Restrictive Conditions

These conditions are characterised by a restrictive pattern of spirometry. They occur due to inflammation which leads to fibrosis (irreversible scarring) of the lungs, meaning they cannot expand fully, reducing the vital capacity. Both the FVC and FEV1 are reduced in restrictive conditions. However, the FEV1/FVC ratio stays constant as both FEV1 and FVC decrease proportionally. Different conditions cause fibrosis predominantly in the upper or lower zones.   Upper Zone Fibrosis (BREASTS) Lower Zone Fibrosis (BRAINS) Berylliosis Bronchiectasis Radiation Rheumatoid Arthritis Extrinsic Allergic Alveolitis Asbestosis Ankylosing spondylitis Idiopathic Pulmonary Fibrosis Silicosis Nitrofurantoin (+ amiodarone, bleomycin, methotrexate) TB Scleroderma Sarcoidosis     Interstitial

Obstructive Conditions

Asthma Asthma is a disease that is characterised by reversible bronchoconstriction, bronchial hyper-responsiveness, and airway inflammation. Allergens induce a Th2 response which stimulates production of IgE and attracts eosinophils to the airways, leading to airway inflammation. This leads to the release of chemical mediators (such as histamine and leukotrienes) which leads to bronchoconstriction increasing airway resistance.   Risk factors Personal or family history of atopic conditions (allergic rhinitis, eczema) Air pollution Precipitants – cold air, allergens (ask about pets, carpet etc.) Drugs – e.g., aspirin intolerant asthma (usually features nasal polyps) Occupational (baking, factory work) – this classically causes reduced peak

LRTIs

Pneumonia This used to describe a lower respiratory tract infection which often occurs when normal defences are impaired It is a blanket term which can be subdivided into a number of types, with different causes and features:   Lobar pneumonia This is characterised by continuous consolidation of a lobe of the lung. It is most frequently due to a bacterial agent, e.g., Streptococcus pneumoniae, Klebsiella pneumoniae, Haemophilus influenzae and Moraxella catarrhalis.   Bronchopneumonia This is characterised by discontinuous areas of consolidation, often bilaterally in the basal lobes, with predominance around the bronchioles. It is usually caused by bacterial agents: Staph

URTIs

Acute epiglottitis This refers to acute inflammation of the epiglottis, which is often caused by the bacteria Haemophilus influenzae type B. It needs to be recognised and treated quickly as it can lead to airway obstruction. It usually presents in children. However, due to the Haemophilus influenzae type B vaccination, its prevalence has decreased.   Symptoms Rapid onset high fever and malaise Drooling of saliva Muffled voice – due to very sore throat Inspiratory stridor (is a high-pitched sound due to turbulent air flow in the upper airway)   Key tests Usually clinical diagnosis, but fibre-optic laryngoscopy may be performed

Head and Neck Conditions

Nasal polyp This is a benign, inflammatory proliferation of the lining of the nose, which usually occurs after recurrent colds (infective sinusitis).   Associations Eosinophilic granulomatosis with polyangiitis Conditions causing poor cilia motility, e.g., cystic fibrosis and primary ciliary dyskinesia (previously known as Kartagener’s syndrome) Samter’s triad – nasal polyps and asthma in conjunction with aspirin sensitivity Symptoms Nasal congestion Rhinorrhoea Changes to taste (ageusia) and smell (anosmia)   Management Steroid spray to reduce size of polyp If remains persistent, refer to ENT for examination and removal   Nasopharyngeal Carcinoma This is a malignant squamous cell tumour of the nasopharynx.

Urinary Tract Infections

This is a general term which describes a bacterial infection anywhere of the urinary tract. It is usually caused by an infection which arises from the enteric bacteria in the gut. It is also classified as uncomplicated (normal renal structure/function) or complicated (producing a structural/functional abnormality of urinary tract)   Risk factors Decreased urine flow – due to dehydration, or obstructions within the urinary tract Increased bacterial entry – due to sexual intercourse, incontinence Higher bacterial growth – diabetes, immunosuppression, catheter use, pregnancy Female – they have a less vertical urethra making bacterial travel easier Key tests Urine dipstick –

Testicular Conditions

Epididymo-orchitis This is inflammation of the epididymis (and the testes)   Causes Bacteria, e.g., chlamydia, gonorrhea, E. coli Viruses, e.g., mumps (in teenage males) Drugs e.g., amiodarone Symptoms Acute onset tender swelling (confined to epididymis) Dysuria, sweats, fever   Management Treat the underlying cause, e.g., antibiotics if due to an STI   Testicular torsion This refers to twisting of the spermatic cord, usually in adolescents It can cut off the blood supply to the testes resulting in ischaemia   Symptoms Acute onset testicular pain Absence of the cremasteric reflex Abdominal pain, nausea and vomiting Prehn’s sign seen (where raising the

Urinary Cancers

Renal Cell Carcinoma (RCC) This refers to a malignant proliferation of kidney cells. It can be sporadic which is associated with increased age, but it is also seen in young children (genetic causes). The most common form is a clear cell carcinoma as the cells look clear on histology   Symptoms Triad of painless hematuria, loin mass and lumbar pain Systemic symptoms e.g., weight loss, fever Paraneoplastic syndromes – due to hormone release, e.g., ACTH, renin, PrPTH Can cause a left-sided varicocele as the tumour may compress the left renal vein   Key tests Ultrasound and CT scan show a

Prostate Conditions

Acute prostatitis This is acute inflammation of the prostate, which usually occurs in infection   Causes Young adults – Chlamydia trachomatis, Neisseria gonorrhoeae Older Adults – E. coli   Symptoms Dysuria, urinary frequency, and suprapubic pain Can cause urinary retention leading to pain and haematospermia Systemic symptoms, e.g., fevers   Key tests DRE gives tender prostate and secretions reveal bacteria   Management Antibiotics e.g. levofloxacin (Quinolone) or Trimethoprim   Benign prostatic hyperplasia (BPH) This refers to hyperplasia of the prostate which occurs with age and is common. It does not increase the risk of cancer, as it is the central

Genetic Conditions

Polycystic kidney disease This is a genetic condition which leads to the development of multiple cysts on the kidneys. It exists as both autosomal dominant and recessive forms:   Autosomal dominant This occurs due to a mutation in the genes PKD1 (Chr 16), or PKD2 (Chr 4) Symptoms Clinically silent initially but gives symptoms in early adulthood  Hypertension (due to renin release), hematuria, cyst infection and kidney failure   Associations Liver cysts (most common extra-renal manifestation) Berry aneurysms in the brain Cardiovascular abnormalities (mitral valve prolapse, valve issues, aortic dissection)   Key tests Abdominal ultrasound is used to detect cysts

Nephrotic Syndrome

This refers to a group of signs and symptoms secondary to glomerular disease. It encompasses damage to the glomerular capillary wall due to a podocyte pathology, leading to abnormal function or podocyte injury/death. It increases permeability to plasma proteins, resulting in albumin loss in the urine. Symptoms Frothy urine – due to loss of protein in urine (>3 g/24 h) Oedema (in ankles, periorbital and scrotum) – this occurs secondary to hypoalbuminemia resulting in decreased oncotic pressure High risk of thrombosis – this is due to loss of endogenous anticoagulants (e.g., antithrombin III) and can give rise to complications including

Nephritic Syndrome

This refers to a group of signs and symptoms secondary to glomerular disease. It reflects inflammatory damage to the glomerulus which increases the permeability to proteins and blood causing proteinuria and haematuria. Left untreated, it can progress to end-stage renal failure. Symptoms Haematuria Less proteinuria (< 3.5 g/24 h) Hypertension and blurred vision Oliguria – low urine output Azotemia – high urea/creatinine Can progress onto renal failure   Key tests Kidney biopsy    There are many specific conditions which give rise to nephritic syndrome, which have specific treatments:   IgA nephropathy This is most common cause of nephritic syndrome, called

Obstructive Renal Conditions

Renal Stones (Nephrolithiasis) This is the presence of a stone which can get lodged somewhere in the urinary tract. It usually in one of the 3 natural points of constriction – pelviureteric junction (PUJ), pelvic brim or vesicoureteric junction (VUJ). There are different types of stones Types of Kidney Stones Risk Factors Dehydration – this increases ion concentration of the urine Recurrent UTIs and foreign bodies which stagnate flow, e.g., stents/catheters Diet – may cause hypercalcaemia and certain foods also increase oxalate levels Underlying metabolic conditions (e.g., hyperparathyroidism)   Symptoms Writhing (colicky) pain which travels from “loin” to groin with

Renal Failure

Acute Kidney Injury (AKI) This is a term which describes a rapid deterioration in renal function, which leads to increased serum urea and creatinine combined with a low urine output. It is very common, occurring in 50% of patients in intensive care units.   There are many different definitions of AKI but the widely used KDIGO criteria are: Rise in creatinine > 26 uM within 48 hours Rise in creatinine > 1.5 Å~ baseline value within 1 week Urine output < 0.5 ml/kg/h for more than 6 consecutive hours   Causes These can be divided into 3 categories: pre-renal, renal

Urinary Cancers

Renal Cell Carcinoma (RCC) This refers to a malignant proliferation of kidney cells. It can be sporadic which is associated with increased age, but it is also seen in young children (genetic causes). The most common form is a clear cell carcinoma as the cells look clear on histology   Symptoms Triad of painless hematuria, loin mass and lumbar pain Systemic symptoms e.g., weight loss, fever Paraneoplastic syndromes – due to hormone release, e.g., ACTH, renin, PrPTH Can cause a left-sided varicocele as the tumour may compress the left renal vein   Key tests Ultrasound and CT scan show a

Prostate Conditions

Acute prostatitis This is acute inflammation of the prostate, which usually occurs in infection   Causes Young adults – Chlamydia trachomatis, Neisseria gonorrhoeae Older Adults – E. coli   Symptoms Dysuria, urinary frequency, and suprapubic pain Can cause urinary retention leading to pain and haematospermia Systemic symptoms, e.g., fevers   Key tests DRE gives tender prostate and secretions reveal bacteria   Management Antibiotics e.g. levofloxacin (Quinolone) or Trimethoprim   Benign prostatic hyperplasia (BPH) This refers to hyperplasia of the prostate which occurs with age and is common. It does not increase the risk of cancer, as it is the central

Renal Tubule Disorders

This is a group of disorders which can affect various parts of the nephron, leading to specific symptoms. The symptoms reflect either an inability to reabsorb or excess reabsorption of solutes in the various segments.  Fanconi syndrome This is a disorder causing impairment of PCT function, preventing solute reabsorption. It can be either inherited or acquired.   Symptoms Glycosuria, aminoaciduria, uricosuria and phosphaturia Phosphate loss can cause bone demineralisation resulting in osteomalacia   Management Phosphate replacement is important   Bartter syndrome This is an inherited condition which results in an impairment of salt reabsorption in the thick ascending loop of

Urinary Tract Infections

This is a general term which describes a bacterial infection anywhere of the urinary tract. It is usually caused by an infection which arises from the enteric bacteria in the gut. It is also classified as uncomplicated (normal renal structure/function) or complicated (producing a structural/functional abnormality of urinary tract)   Risk factors Decreased urine flow – due to dehydration, or obstructions within the urinary tract Increased bacterial entry – due to sexual intercourse, incontinence Higher bacterial growth – diabetes, immunosuppression, catheter use, pregnancy Female – they have a less vertical urethra making bacterial travel easier Key tests Urine dipstick –

Acute Kidney Injury (AKI)

This is a term which describes a rapid deterioration in renal function, which leads to increased serum urea and creatinine combined with a low urine output. It is very common, occurring in 50% of patients in intensive care units.   There are many different definitions of AKI but the widely used KDIGO criteria are: Rise in creatinine > 26 uM within 48 hours Rise in creatinine > 1.5 Å~ baseline value within 1 week Urine output < 0.5 ml/kg/h for more than 6 consecutive hours   Causes These can be divided into 3 categories: pre-renal, renal and post-renal:   Pre-renal

Urinary Tract Infections

This is a general term which describes a bacterial infection anywhere of the urinary tract. It is usually caused by an infection which arises from the enteric bacteria in the gut. It is also classified as uncomplicated (normal renal structure/function) or complicated (producing a structural/functional abnormality of urinary tract)   Risk factors Decreased urine flow – due to dehydration, or obstructions within the urinary tract Increased bacterial entry – due to sexual intercourse, incontinence Higher bacterial growth – diabetes, immunosuppression, catheter use, pregnancy Female – they have a less vertical urethra making bacterial travel easier Key tests Urine dipstick –

Nephritic Syndrome

This refers to a group of signs and symptoms secondary to glomerular disease. It reflects inflammatory damage to the glomerulus which increases the permeability to proteins and blood causing proteinuria and haematuria. Left untreated, it can progress to end-stage renal failure. Symptoms Haematuria Less proteinuria (< 3.5 g/24 h) Hypertension and blurred vision Oliguria – low urine output Azotemia – high urea/creatinine Can progress onto renal failure   Key tests Kidney biopsy    There are many specific conditions which give rise to nephritic syndrome, which have specific treatments:   IgA nephropathy This is most common cause of nephritic syndrome, called

Nephrotic Syndrome

This refers to a group of signs and symptoms secondary to glomerular disease. It encompasses damage to the glomerular capillary wall due to a podocyte pathology, leading to abnormal function or podocyte injury/death. It increases permeability to plasma proteins, resulting in albumin loss in the urine. Symptoms Frothy urine – due to loss of protein in urine (>3 g/24 h) Oedema (in ankles, periorbital and scrotum) – this occurs secondary to hypoalbuminemia resulting in decreased oncotic pressure High risk of thrombosis – this is due to loss of endogenous anticoagulants (e.g., antithrombin III) and can give rise to complications including

Renal Failure

Acute Kidney Injury (AKI) This is a term which describes a rapid deterioration in renal function, which leads to increased serum urea and creatinine combined with a low urine output. It is very common, occurring in 50% of patients in intensive care units.   There are many different definitions of AKI but the widely used KDIGO criteria are: Rise in creatinine > 26 uM within 48 hours Rise in creatinine > 1.5 Å~ baseline value within 1 week Urine output < 0.5 ml/kg/h for more than 6 consecutive hours   Causes These can be divided into 3 categories: pre-renal, renal

Control of Potassium

We need to regulate potassium as it determines the resting membrane potential. – As the relative permeabilities of sodium and calcium are very low, K+ is the main determinant. – Normal extracellular [K+] = 4mM – Intracellular [K+] = 125mM – As the extracellular space much smaller than intracellular 16:24 litres, changes in [K+] extracellular affect Em greatly.   Why K+ changes The Potassium concentration can change for many reasons: – Changes in intake –> average of 100mM K+ eaten per day, but starvation may decrease this – Inability to absorb it –> inflammation of the bowel – Excessive loss –> 

Control of pH

We need to regulate pH as the function of enzymes and cell surface ion channels are affected by [H+]. – In addition, bone buffers [H+], so an increase in [H+] will demineralize bone – An acidosis also may lead to a potassium extracellular shift causing hyperkalaemia.   The main way body pH is controlled is by buffering [H+] ions by the bicarbonate buffer system. When [H+] ions are added, they are buffered by HCO3 ions and excreted by the lungs as CO2. However, this is not sustainable unless the kidneys also produce HCO3 ions to replace the ones that are lost.  

Male Anatomy

Testes These are the main male reproductive organs which are suspended in the scrotum on the pedicles of the spermatic cords. – These hang outside the body as the lower temperature is needed for effective spermatogenesis – They develop from the posterior abdominal wall and carry peritoneum as they migrate through the inguinal canal. – This peritoneum forms a double layer (tunica vaginalis) around the testes. – The residual connection to the peritoneal cavity is obliterated as the processus vaginalis. – Testes are also covered by outer fibrous tunica albuginea – At the head of the testis is the epididymis,

Renal Anatomy

The kidneys lie with their hila at the level L1, with the right kidney being lower – Kidneys are retroperitoneal organs so access is often obtained from the back – The kidneys are enclosed in a fibrous capsule and embedded in perinephric fat.   The kidney is composed of an outer region called the cortex and a central medulla. – The medulla is formed of renal pyramids –> converge on calyces –> inner pelvis – The pelvis then continues on as the ureter carrying urine to the bladder.   Blood supply The kidney is perfused by the renal arteries, which

Penis Conditions

Hypospadias This is a developmental condition where the urethra opens on the under surface of the penis shaft, rather than the tip of the glans. It occurs when the urethral folds fail to close. Management Surgical correction is the definitive treatment   Epispadias This is a developmental condition where the urethra opens on the upper surface of the penis shaft, rather than tip of the glans. It can be due to wrong positioning of the genital tubercle.   Management Surgical correction   Balanitis This is acute inflammation of the foreskin and glans, usually due to infection Can also be due

Prostate Conditions

Acute prostatitis This is acute inflammation of the prostate, which usually occurs in infection   Causes Young adults – Chlamydia trachomatis, Neisseria gonorrhoeae Older Adults – E. coli   Symptoms Dysuria, urinary frequency, and suprapubic pain Can cause urinary retention leading to pain and haematospermia Systemic symptoms, e.g., fevers   Key tests DRE gives tender prostate and secretions reveal bacteria   Management Antibiotics e.g. levofloxacin (Quinolone) or Trimethoprim   Benign prostatic hyperplasia (BPH) This refers to hyperplasia of the prostate which occurs with age and is common. It does not increase the risk of cancer, as it is the central

General biology

Q1. In the complete year, Rabi Crops are grown in which season? Spring Rainy Summer Winter Ans. Winter   Q2. Rhizobium Bacteria which fixes atmospheric nitrogen are found in nodules growing in: Leaves of leguminous plants Roots of leguminous plants Stem of leguminous plants All options are correct Ans. Roots of leguminous plants   Q3. The grain seed is separated from the chaff in the harvested crop. The process is called as: Seeding Weeding Threshing Ploughing Ans. Threshing   Q4. Select the examples of Multicellular Microorganism from the following: Algae and Fungi Algae and Bacteria Bacteria and Viruses Bacteria and

Prostate Conditions

Acute prostatitis This is acute inflammation of the prostate, which usually occurs in infection   Causes Young adults – Chlamydia trachomatis, Neisseria gonorrhoeae Older Adults – E. coli   Symptoms Dysuria, urinary frequency, and suprapubic pain Can cause urinary retention leading to pain and haematospermia Systemic symptoms, e.g., fevers   Key tests DRE gives tender prostate and secretions reveal bacteria   Management Antibiotics e.g. levofloxacin (Quinolone) or Trimethoprim   Benign prostatic hyperplasia (BPH) This refers to hyperplasia of the prostate which occurs with age and is common. It does not increase the risk of cancer, as it is the central

Testicular Conditions

Epididymo-orchitis This is inflammation of the epididymis (and the testes)   Causes Bacteria, e.g., chlamydia, gonorrhea, E. coli Viruses, e.g., mumps (in teenage males) Drugs e.g., amiodarone Symptoms Acute onset tender swelling (confined to epididymis) Dysuria, sweats, fever   Management Treat the underlying cause, e.g., antibiotics if due to an STI   Testicular torsion This refers to twisting of the spermatic cord, usually in adolescents It can cut off the blood supply to the testes resulting in ischaemia   Symptoms Acute onset testicular pain Absence of the cremasteric reflex Abdominal pain, nausea and vomiting Prehn’s sign seen (where raising the

Genetic Conditions

Polycystic kidney disease This is a genetic condition which leads to the development of multiple cysts on the kidneys. It exists as both autosomal dominant and recessive forms:   Autosomal dominant This occurs due to a mutation in the genes PKD1 (Chr 16), or PKD2 (Chr 4) Symptoms Clinically silent initially but gives symptoms in early adulthood  Hypertension (due to renin release), hematuria, cyst infection and kidney failure   Associations Liver cysts (most common extra-renal manifestation) Berry aneurysms in the brain Cardiovascular abnormalities (mitral valve prolapse, valve issues, aortic dissection)   Key tests Abdominal ultrasound is used to detect cysts

Urinary Cancers

Renal Cell Carcinoma (RCC) This refers to a malignant proliferation of kidney cells. It can be sporadic which is associated with increased age, but it is also seen in young children (genetic causes). The most common form is a clear cell carcinoma as the cells look clear on histology   Symptoms Triad of painless hematuria, loin mass and lumbar pain Systemic symptoms e.g., weight loss, fever Paraneoplastic syndromes – due to hormone release, e.g., ACTH, renin, PrPTH Can cause a left-sided varicocele as the tumour may compress the left renal vein   Key tests Ultrasound and CT scan show a

Renal Tubule Disorders

Renal Stones (Nephrolithiasis) This is the presence of a stone which can get lodged somewhere in the urinary tract. It usually in one of the 3 natural points of constriction – pelviureteric junction (PUJ), pelvic brim or vesicoureteric junction (VUJ). There are different types of stones Types of Kidney Stones Risk Factors Dehydration – this increases ion concentration of the urine Recurrent UTIs and foreign bodies which stagnate flow, e.g., stents/catheters Diet – may cause hypercalcaemia and certain foods also increase oxalate levels Underlying metabolic conditions (e.g., hyperparathyroidism)   Symptoms Writhing (colicky) pain which travels from “loin” to groin with

Fibre to Fabric

1. Which one of the following is a synthetic fibre? a.) Rayon b.) Nylon c.) Polyester d.) All of the above Answer – (d.) All of the above Explanation – Synthetic fibres are man-made polymers that are used to create fabric. Polymers are formed when many small units are chemically joined together.   2. The process of separating cotton fibres from the seeds is called ____. a.) Retting b.) Ginning c.) Weaving d.) Spinning Answer – (b.) Ginning Explanation – Ginning is the process of separating cotton fibres from cotton seeds or lint. It also aids in the removal of

Psychotic Disorders

Psychosis is the misrepresentation of thoughts and perceptions that originate from a patient’s own mind which are experienced as reality. It is a symptom, not a diagnosis in itself and affects about 3% of the population.   Causes: With most psychiatric conditions, the aetiology of psychosis is seen with a biopsychosocial model: Biological: Genetics –> Twin studies have shown schizophrenia has 50% concordance rate in MZ  twins Dopamine–> Antipsychotics block D2 receptors whereas L-Dopa induces psychosis Neurodevelopmental –> Higher in people with low birth weight, developmental delay etc.   Psychological: Prodrome –> Often preceded by patients exhibiting anxiety, depression and ideas of reference –

Stress Reactions

  Acute stress reaction This is an acute reaction which occurs rapidly (minutes to hours) after a sudden and stressful event. – This can include sexual assault, an injury, a near-death experience etc. – This leads to several symptoms in response which usually arise very quickly and terminate within 3 days   Symptoms: – Initial state of being dazed and confused – Purposeless overactivity and withdrawal – Intense brief anxiety – Autonomic arousal –> sweating, dry mouth, vomiting   Management – Help patient to re-orientate with trauma-focussed CBT Prognosis – Most cases resolve rapidly within 3 days. If symptoms persist > 1

Affective Disorders

Affective (mood disorders) are characterised by emotional disturbances resulting in functional impairment.   Causes: The aetiology of affective disorders can be seen using a biopsychosocial model:  Biological: 5-HT–> Low levels of endogenous 5-HT and Na are thought to decrease mood Cortisol –> Overactivation of the HPA axis increases both risk and persistence of low  mood   Psychological: Beck’s triad –> Negative views about the self, the world and the future seen in depression Attributional style –> Higher incidence in people who blame themselves for life events   Social: Stress –> Linked to negative life events, adversity and childhood stress.   Depression This is a mental

Medically Unexplained Symptoms

  Somatisation Disorder (SYMPTOMS) This is a disorder where patients believe that have physical symptoms present for at least 2 years, despite no physical or organic explanation – The most common symptoms mentioned usually involve the GI tract (abdominal pain) or the skin – Patients don’t accept negative test results and instead feel great distress and worry over their symptoms – It is more common in young women and can lead to multiple operations/investigations despite absence of disease   Hypochondrial Disorder (DISEASE) This is a disorder where patients believe they have a serious underlying disease e.g. cancer, HIV, AIDS –

Affective Disorders

Affective (mood disorders) are characterised by emotional disturbances resulting in functional impairment.   Causes: The aetiology of affective disorders can be seen using a biopsychosocial model:  Biological: 5-HT–> Low levels of endogenous 5-HT and Na are thought to decrease mood Cortisol –> Overactivation of the HPA axis increases both risk and persistence of low  mood   Psychological: Beck’s triad –> Negative views about the self, the world and the future seen in depression Attributional style –> Higher incidence in people who blame themselves for life events   Social: Stress –> Linked to negative life events, adversity and childhood stress.   Depression This is a mental

Delirium

This is an acute confusional state which is characterised by rapid onset of a global but fluctuating dysfunction of the CNS due to a variety of insults on the brain. – It is more commonly seen in people aged >65 and those with diffuse brain disease (dementia) – However, it can be experienced by anyone in hospital and is an important thing to keep watch out for   Causes – The main causes can be remembered using the acronym PINCH-ME: P – Pain In – Infection (often a UTI in elderly) C – Constipation H – Hydration M – Medication (drugs) E – Electrolytes (e.g. hyponatraemia) E – Environment

Medically Unexplained Symptoms

  Somatisation Disorder (SYMPTOMS) This is a disorder where patients believe that have physical symptoms present for at least 2 years, despite no physical or organic explanation – The most common symptoms mentioned usually involve the GI tract (abdominal pain) or the skin – Patients don’t accept negative test results and instead feel great distress and worry over their symptoms – It is more common in young women and can lead to multiple operations/investigations despite absence of disease   Hypochondrial Disorder (DISEASE) This is a disorder where patients believe they have a serious underlying disease e.g. cancer, HIV, AIDS –

Eating Disorders

  Eating disorders refer to a group of conditions which are characterised by a disorganised pattern of food consumption which causes physical and emotional distress. – They are more common in females than males (3:1) with an onset around age 15-30. – The two most common are anorexia nervosa and bulimia nervosa, which share similar features.   Causes: With most psychiatric conditions, the aetiology can be considered using a biopsychosocial model. Biological: Genetics –> Twin studies have shown that eating disorders share a large genetic component 5-HT –> Altered brain serotonin contributes to dysregulation of appetite, mood and impulsivity   Psychological: Personality –> Higher

Personality Disorders

Personality is “the range of characteristic behavioural responses that a person deploys in order to negotiate the challenges produced by the outside world and their internal feelings.” – It is composed of 4 main components: cognition, impulse control, social communication and affect/emotions – As these components are continuous, psychiatrists assign cut-offs indicating when they become abnormal.   A personality disorder is where one or more of these components of personality has reached an abnormal level: i) The trait has to be pathological, pervasive and persistent (3P’s) ii) It must lead to stereotyped responses which can be traced to childhood iii)

Affective Disorders

  Affective (mood disorders) are characterised by emotional disturbances resulting in functional impairment.   Causes: The aetiology of affective disorders can be seen using a biopsychosocial model:  Biological: 5-HT–> Low levels of endogenous 5-HT and Na are thought to decrease mood Cortisol –> Overactivation of the HPA axis increases both risk and persistence of low  mood   Psychological: Beck’s triad –> Negative views about the self, the world and the future seen in depression Attributional style –> Higher incidence in people who blame themselves for life events   Social: Stress –> Linked to negative life events, adversity and childhood stress.   Depression This is a

Affective Disorders

Affective (mood disorders) are characterised by emotional disturbances resulting in functional impairment.   Causes: The aetiology of affective disorders can be seen using a biopsychosocial model:  Biological: 5-HT–> Low levels of endogenous 5-HT and Na are thought to decrease mood Cortisol –> Overactivation of the HPA axis increases both risk and persistence of low  mood   Psychological: Beck’s triad –> Negative views about the self, the world and the future seen in depression Attributional style –> Higher incidence in people who blame themselves for life events   Social: Stress –> Linked to negative life events, adversity and childhood stress.   Depression This is a mental

Eating Disorders

Eating disorders refer to a group of conditions which are characterised by a disorganised pattern of food consumption which causes physical and emotional distress. – They are more common in females than males (3:1) with an onset around age 15-30. – The two most common are anorexia nervosa and bulimia nervosa, which share similar features.   Causes: With most psychiatric conditions, the aetiology can be considered using a biopsychosocial model. Biological: Genetics –> Twin studies have shown that eating disorders share a large genetic component 5-HT –> Altered brain serotonin contributes to dysregulation of appetite, mood and impulsivity   Psychological: Personality –> Higher association

Substance Abuse

Alcohol Alcohol abuse is defined as the regular or binge consumption of alcohol which can lead to physical, neuropsychiatric or social damage. – 1 unit (10mL) of alcohol is about equivalent to a small glass of wine, or a single peg of spirits. – Units = Volume (L) * ABV (%) – e.g. a 750ml bottle of wine, strength 12% has 750/1000 *12 = 9 units – Both men and women should drink no more than 14 units a week. If you do, it is best to spread this evenly over 3 days or more. There are several problems of

Childhood Conditions

ADHD This is a disorder which is characterised by inattention, hyperactivity and impulsivity – It is much more common in boys than girls and diagnosed in the primary school years – In order to distinguish this condition from simply bad behaviour, there are 3 key things that must be present in order to satisfy the diagnostic criteria: –> Persistent – This means that the disruptive behaviour must be constant – If behaviour does fluctuate, then this could simply be an acute reaction to a change in the environment of the child.   –> Pervasive – This means that the disruptive behaviour must be seen

Childhood Conditions

  ADHD This is a disorder which is characterised by inattention, hyperactivity and impulsivity – It is much more common in boys than girls and diagnosed in the primary school years – In order to distinguish this condition from simply bad behaviour, there are 3 key things that must be present in order to satisfy the diagnostic criteria: –> Persistent – This means that the disruptive behaviour must be constant – If behaviour does fluctuate, then this could simply be an acute reaction to a change in the environment of the child.   –> Pervasive – This means that the disruptive behaviour must be

Medically Unexplained Symptoms

  Somatisation Disorder (SYMPTOMS) This is a disorder where patients believe that have physical symptoms present for at least 2 years, despite no physical or organic explanation – The most common symptoms mentioned usually involve the GI tract (abdominal pain) or the skin – Patients don’t accept negative test results and instead feel great distress and worry over their symptoms – It is more common in young women and can lead to multiple operations/investigations despite absence of disease   Hypochondrial Disorder (DISEASE) This is a disorder where patients believe they have a serious underlying disease e.g. cancer, HIV, AIDS –

Substance Abuse

Alcohol Alcohol abuse is defined as the regular or binge consumption of alcohol which can lead to physical, neuropsychiatric or social damage. – 1 unit (10mL) of alcohol is about equivalent to a small glass of wine, or a single peg of spirits. – Units = Volume (L) * ABV (%) – e.g. a 750ml bottle of wine, strength 12% has 750/1000 *12 = 9 units – Both men and women should drink no more than 14 units a week. If you do, it is best to spread this evenly over 3 days or more. There are several problems of

Eating Disorders

  Eating disorders refer to a group of conditions which are characterised by a disorganised pattern of food consumption which causes physical and emotional distress. – They are more common in females than males (3:1) with an onset around age 15-30. – The two most common are anorexia nervosa and bulimia nervosa, which share similar features.   Causes: With most psychiatric conditions, the aetiology can be considered using a biopsychosocial model. Biological: Genetics –> Twin studies have shown that eating disorders share a large genetic component 5-HT –> Altered brain serotonin contributes to dysregulation of appetite, mood and impulsivity   Psychological: Personality –> Higher

Dementia

The commonest aetiologies of dementia are: Alzheimer’s disease, Vascular and Lewy body dementia. – These conditions are difficult to diagnose and there are many assessment tools e.g. GPCOG, abbreviated mental test score (AMTS) and the mini-mental state examination (MMSE)   Investigation pathway: – 1st do a cognitive assessment e.g. MOCA – Exclude reversible causes – do FBC, U&E, LFTs, calcium, glucose, TFT, Vit B12 and folate (2) – Imaging – CT head (structural causes) and MRI (vasculature changes)    Alzheimer’s disease The number one cause of dementia in the UK is Alzheimer’s disease. The disease is characterised by a progression degeneration

Delirium

  This is an acute confusional state which is characterised by rapid onset of a global but fluctuating dysfunction of the CNS due to a variety of insults on the brain. – It is more commonly seen in people aged >65 and those with diffuse brain disease (dementia) – However, it can be experienced by anyone in hospital and is an important thing to keep watch out for   Causes – The main causes can be remembered using the acronym PINCH-ME: P – Pain In – Infection (often a UTI in elderly) C – Constipation H – Hydration M – Medication (drugs) E – Electrolytes (e.g. hyponatraemia) E –

Psychotic Disorders

  Psychosis is the misrepresentation of thoughts and perceptions that originate from a patient’s own mind which are experienced as reality. It is a symptom, not a diagnosis in itself and affects about 3% of the population.   Causes: With most psychiatric conditions, the aetiology of psychosis is seen with a biopsychosocial model: Biological: Genetics –> Twin studies have shown schizophrenia has 50% concordance rate in MZ  twins Dopamine–> Antipsychotics block D2 receptors whereas L-Dopa induces psychosis Neurodevelopmental –> Higher in people with low birth weight, developmental delay etc.   Psychological: Prodrome –> Often preceded by patients exhibiting anxiety, depression and ideas of reference

Stress Reactions

Acute stress reaction This is an acute reaction which occurs rapidly (minutes to hours) after a sudden and stressful event. – This can include sexual assault, an injury, a near-death experience etc. – This leads to several symptoms in response which usually arise very quickly and terminate within 3 days   Symptoms: – Initial state of being dazed and confused – Purposeless overactivity and withdrawal – Intense brief anxiety – Autonomic arousal –> sweating, dry mouth, vomiting   Management – Help patient to re-orientate with trauma-focussed CBT Prognosis – Most cases resolve rapidly within 3 days. If symptoms persist > 1 month,

Affective Disorders

  Affective (mood disorders) are characterised by emotional disturbances resulting in functional impairment.   Causes: The aetiology of affective disorders can be seen using a biopsychosocial model:  Biological: 5-HT–> Low levels of endogenous 5-HT and Na are thought to decrease mood Cortisol –> Overactivation of the HPA axis increases both risk and persistence of low  mood   Psychological: Beck’s triad –> Negative views about the self, the world and the future seen in depression Attributional style –> Higher incidence in people who blame themselves for life events   Social: Stress –> Linked to negative life events, adversity and childhood stress.   Depression This is a

Mental State Examination

The mental state examination is a way of observing and describing a patient’s current state of mind. – The purpose of the MSE is to get a cross-sectional description of the patient’s mental state – It is a time-specific snapshot of the patient’s current mental state (allows comparison to before) – This is combined with the psychiatric history, allowing clinicians to get the overall sense of the patient’s condition   Mental State Exam Acronym = A Brilliant Scientist Makes All Theories Too Perfectly Complicated “In-it”   Appearance This is a general description of the patient’s general look and appearance. Important to include the following: – An opening sentence summarising

Psychotherapy

Psychotherapy works by helping people understand why they feel as they do. It uses a combination of reflecting about past events, learning new coping strategies and building a therapist-patient relationship. – There are 3 main areas of psychological therapy, each with its advantages and disadvantages: i) Supportive therapies e.g. Counselling + Supportive Psychotherapy This is the least intense level of psychotherapy which is used for mild depression and anxiety – The sessions are unstructured but allow the patient to establish rapport, reflect and get reassurance – It is a non-direct way of solving the problem –> works for stress, bereavement,

Mental Health Act

The main piece of mental health legislation in England is the Mental Health Act 1983. This was amended by the Mental Health Act 2007.   Who it applies to? The Mental Health act applies to people with a “mental disorder” – any disorder/disability of mind – However, it excludes anyone with dependence on drugs or alcohol – Also excludes patients with learning disability, unless their condition causes abnormally aggressive or seriously irresponsible conduct – Applies to people of any age, but children are usually treated with consent of their parent.   Sectioning (compulsory admission to hospital) This part allows admission

Mental Capacity Act

Mental Capacity can be defined as the ability to make your own decisions. – This is very important as it gives patients autonomy and the right to make choices about their own healthcare – It becomes complicated when people lack capacity, as others have to make decisions about patients – The Mental Capacity act applied to people aged 16 and over. If the child is younger than 16, they only have capacity to make decisions provided that they are Gillick Competent.   5 key principles of mental capacity: i) A person is assumed to have capacity is assumed until it

Diagnoses in Psychiatry

Disease = the objective physical pathology and known aetiology Illness = the patient’s subjective distress caused by a condition   A big problem in psychiatry is that many conditions have no known or understood pathophysiological cause. – This makes it very difficult to diagnose diseases, since there is no demonstrable pathology. – Therefore, psychiatry talks about mental illness – this is a level of subjective distress which is greater in severity or duration than occurs in normal human experience – This allows us to diagnose patients regardless of our understanding of the condition and provide treatment   A diagnosis is the art

Renal Conditions

Vesicoureteral reflux This is the backflow of urine from the bladder into the ureter, which is divided into 2 types. – The backflow of urine predisposes children to recurrent infections which can later lead to renal scarring. – If left untreated, it is a risk factor for later developing progressive chronic kidney disease and hypertension   Primary VUR This is the most common type, which occurs due to a congenital defect in the vesicoureteral junction – This defect causes the ureters to enter the bladder in a more perpendicular fashion – This reduces the length of the ureter in the

Right-to-left Shunts

These conditions lead to the mixing of deoxygenated blood from the right side of the circulation and oxygenated blood in the left side of the circulation. – This leads to cyanosis, which can be divided into two types:   i) Peripheral cyanosis: – This occurs in the extremities such as feet and hands, is very common in the first 24 hours of life – It can also occur when the child is crying or unwell from any cause, and so is less serious   ii) Central cyanosis: – This is seen when the concentration of reduced haemoglobin in the blood

Prematurity

A premature infant is defined as a baby that is born alive before 37 weeks, which can be split into categories. – Antenatally, mothers are given magnesium sulphate (neuroprotective) and steroids to stimulate lung maturation – Extremely preterm = <28 weeks (these need transfer to tertiary centre) – Very preterm = 28 – 32 weeks – Moderate – Late preterm = 32-37 weeks   Premature babies are expected to have delayed developmental milestones. Therefore, to track their development, we need to correct the baby’s age according to how premature they were to see whether they are delayed from their expected

Bone Tumours

Bone tumours occur due to an abnormal proliferation of bone cells, and these can be either benign or malignant. – One of the most common symptoms that bone cancers produce is bone pain. However, this is a very ambiguous symptoms as bone pain can be poorly localised and due to many differentials. – Therefore, it is important to look out for particular red flags which may indicate bone cancer. Red Flag Symptoms Guidelines: – For unexplained bone pain/swelling in children and young people –> urgent X-ray within 48 hours – If results suggest sarcoma –> referral to specialist within 2

Prematurity

A premature infant is defined as a baby that is born alive before 37 weeks, which can be split into categories. – Antenatally, mothers are given magnesium sulphate (neuroprotective) and steroids to stimulate lung maturation – Extremely preterm = <28 weeks (these need transfer to tertiary centre) – Very preterm = 28 – 32 weeks – Moderate – Late preterm = 32-37 weeks   Premature babies are expected to have delayed developmental milestones. Therefore, to track their development, we need to correct the baby’s age according to how premature they were to see whether they are delayed from their expected

Neonatal Conditions

Transient Tachypnoea of the New-born (TTN) This is a condition which is the most common cause of respiratory distress in babies. – In the fetus, the lungs are filled with fluid, however this normally gets squeezed out during vaginal birth and the remainder gets absorbed shortly after birth into the bloodstream. – The problem arises when there is a delay in the reabsorption of lung fluid, which “drowns” lungs – A risk factor is C-section delivery (as fluid is not squeezed out of the lungs)   Symptoms: – Respiratory distress (tachypnoea, tachycardia, breathlessness)   Diagnosis: – Diagnosis of exclusion once

Epilepsy

Early Childhood (infancy – 2 years)   Benign sleep myoclonus These are myoclonic jerks that occur during sleep in young children, which stop if the child is woken up – They are complete benign and not real seizures and self-limiting, so only need to provide reassurance to parents.   Infantile spasms (West’s syndrome) This is a rare form of epilepsy in children which is usually 2nd to a serious neurological abnormality. – it is thought to be due to malfunction of the regulation of GABA transmission   Symptoms: – Triad of muscle spasm attacks – Lightning attacks –> (rapid flexion

Trisomies

Down’s syndrome This condition is caused by having an extra chromosome 21 leading to multiple complications   Inheritance: – Trisomy 21 (the risk of this increases with maternal age), – Some cases due to Robertsonian chromosome translocation (usually onto 14) – can be inherited   Risk: The risk of Down’s syndrome increases with maternal age. – Maternal age 20 – 1in 1500 – Maternal age 45 – 1 in 50  Maternal Age (years)  20  50  40  45  Risk  1 in 1500  1 in 800  1 in 100  1 in 50 Symptoms: Intellectual –> Learning disability, autism, early onset Alzheimer’s disease, delayed

Disorders of Sexual Development

There are host of conditions which may interfere with androgen signalling, which can lead to disorders of sexual development.   Congenital Adrenal Hyperplasia (CAH) This is an autosomal recessive disorder which causes an excess of sex steroids with hyperplasia of both adrenal glands. – It occurs due to a mutation in the enzymes which catalyse aldosterone and cortisol synthesis. – Deficiency in these enzymes means that the precursors get shunted towards sex steroid production leading to increase in androgens, leading to the masculinisation of individuals – In addition, Cortisol deficiency leads to high ACTH (lack of negative feedback), giving bilateral

Hip Conditions

Developmental Dysplasia of the hip (DDH) This represents a spectrum of conditions which affect the proximal femur and acetabulum, seen in new-borns – The junction between femur and acetabulum is not properly formed which results in deformity which can range from mild dysplasia to subluxation and full dislocation of the hip – It is much more common in females and more common in the left hip – The biggest risk factor is breech presentation, as well as a positive family history and oligohydramnios – Therefore, all breech babies born at 36+ weeks gestation require bilateral hip ultrasound scan at 6

Nausea and Vomiting

Gastro-oesophageal reflux disease (GORD) In children, Gastro-oesophageal reflux refers to the passage of gastric contents into the oesophagus. – Reflux is a common event and is self-limiting, with nearly all cases resolving spontaneously by 12 months. – It is characterised by vomiting/regurgitation after feeds but normal weight gain and growth – It is common in children due to a host of factors, such as inappropriate relaxation of the LOS because of functional immaturity, a short intra-stomach length of the oesophagus and a predominantly fluid-based diet   The term GORD refers to GOR that causes symptoms severe enough to merit medical treatment

Specific Infections

Scarlet Fever This is a systemic reaction to the toxin made by Group A haemolytic streptococci (usually S. pyogenes) – The infection usually occurs in children around the ages of 3-5 and it is a notifiable disease – The bacteria can be spread by inhalation of droplets or by direct contact through secretions – It affects a small number of people who have the strep throat or skin infection (impetigo) Symptoms: – General –> fever, malaise, headache, sore throat, swollen lymph nodes – Strawberry tongue – this initially has a white coating on it, after which red papillae poke through

Respiratory Tract Infections

Bronchiolitis This is a lower respiratory tract infection which leads to the blockage of small airway in the lungs – It can lead to significant respiratory distress, especially in children with other comorbidities such as prematurity, congenital heart disease or immunodeficiency. – It is most seen in children younger than 2 and cases spike in autumn and winter   Cause: Respiratory syncytial virus (most common), rhinovirus is second most common cause   Symptoms: – General –> coryza, fever, irritability, poor feeding – Dry cough – Coryzal symptoms precede – Wheeze and crackles on auscultation – Respiratory distress –> chest wall

Liver Conditions

One of the main symptoms of paediatric liver conditions is jaundice. Whilst neonatal jaundice is a common finding, jaundice in the first 24 hours is always pathological. – This may be due to haemolytic disorders, infection, or metabolic liver disorders like Crigler-Najjar syndrome. – The problem with this is that is can lead to raised levels of unconjugated bilirubin in the blood. – As this is fat soluble, it can cross the blood brain barrier is very neurotoxic and cause irreversible neurological symptoms.    Biliary Atresia This is a condition where there is progressive fibrosis and obliteration of the biliary

Prematurity

A premature infant is defined as a baby that is born alive before 37 weeks, which can be split into categories. – Antenatally, mothers are given magnesium sulphate (neuroprotective) and steroids to stimulate lung maturation – Extremely preterm = <28 weeks (these need transfer to tertiary centre) – Very preterm = 28 – 32 weeks – Moderate – Late preterm = 32-37 weeks   Premature babies are expected to have delayed developmental milestones. Therefore, to track their development, we need to correct the baby’s age according to how premature they were to see whether they are delayed from their expected

Neonatal Conditions

Transient Tachypnoea of the New-born (TTN) This is a condition which is the most common cause of respiratory distress in babies. – In the fetus, the lungs are filled with fluid, however this normally gets squeezed out during vaginal birth and the remainder gets absorbed shortly after birth into the bloodstream. – The problem arises when there is a delay in the reabsorption of lung fluid, which “drowns” lungs – A risk factor is C-section delivery (as fluid is not squeezed out of the lungs)   Symptoms: – Respiratory distress (tachypnoea, tachycardia, breathlessness)   Diagnosis: – Diagnosis of exclusion once