Author Archives: Ken Ekechukwu

Percutaneous gastrostomy. Ken U. Ekechukwu, MD, MPH, FACP.

What is percutaneous gastrostomy?
Per is Latin for through. Cutaneous comes from cutis, Latin for skin. Gastro derives from gaster, Greek for stomach. Stomy is from stomatos, Greek for mouth. Thus, ‘percutaneous gastrostomy’ means making a hole (or opening/mouth) in the stomach through the skin. It is the deliberate construction of a track from the skin to the stomach through which a feeding tube or catheter is inserted into the stomach to provide an access for nourishing a patient, bypassing the mouth and the esophagus.

How is percutaneous gastrostomy done?
The patient will have nothing by mouth starting the midnight preceding the procedure. This empties the stomach, allowing a clean field and the use of sedation for the procedure. The patient is taken to the interventional radiology (IR) suit on the morning of the procedure and placed on a procedure table. A nurse or the physician sprays a local anesthetic at the back of the patient’s throat to numb it. Then a tube is passed through the mouth into the stomach so it can be inflated with air. Sometimes this is done on the floor before the patient arrives the IR suite. The upper part of the abdomen and the lower chest are scrubbed with antiseptic lotion to prevent wound or blood infection. The patient receives a prophylactic  intravenous antibiotic and medications for conscious sedation. Then another intravenous medicine is given to temporarily slow movements of the stomach and the intestines and keep air in the stomach. The stomach is filled with air through the tube in it and a small cut is made on the anesthetized skin over the mid or lower stomach. A needle is passed through the skin incision into the stomach, through which 2 or 3 T-shaped fasteners are deployed into the stomach. These fix the anterior wall of the stomach against the posterior surface of the anterior abdominal wall and keep the stomach from slipping away during later maneuvers. A wire is passed through the needle into the stomach and dilators are passed over the wire to dilate the needle track. Then a feeding tube is passed over the wire into the stomach and anchored to the skin. Finally, iodinated radiocontrast is injected into the stomach through the tube to confirm that the tip of the tube is in the stomach and that there is no leakage around it. A collecting bag  is attached to the tube to collect air and liquid for 12 to 24 hours to make sure that all is well. The tube may be used thereafter, if all is well.

Who needs percutaneous gastrostomy?
1. Those who cannot eat food by mouth for more than 30 days for any reason.
2. Those whose stomach has difficulty emptying itself.

What are the contraindications to percutaneous gastrostomy?
Contraindications to percutaneous gastrostomy are conditions that make the procedure a hazard. They include the following:
1. Uncorrectable coagulopathy. This means ‘thinning’ of the blood that predisposes to hemorrhage during or after the procedure. 
2. No safe access. Scars from past surgery or injury to the abdomen can distort the intra-abdominal anatomy. 
3. Gastric tumors. Gastric cancer can grow through the gastrostomy track to the surface of the abdomen, if the track was unwittingly created close to or through the cancer.
4. Abdominal varices. These are large collateral or bypass blood vessels on or in the abdomen that can be injured during gastrostomy. They may occur in patients with cirrhosis of the liver or total obstruction of the inferior and superior vena cava. 
5. Massive ascites. The abdomen is full of liquid due to failure of the liver, the kidneys or the heart; it is a relative contraindication, because the fluid can be emptied shortly before the procedure.
6. Ventriculoperitoneal shunt. A small tube connects the ventricles in the brain with the peritoneal cavity in the abdomen. The shunt can become infected and the infection spread up the tube into the brain; it, too, is a relative contraindication.
7. Severe gastroesophageal reflux. The cause of heart burn. In this case the tip of your tube should be placed past the stomach to avoid inundating the stomach with liquid that may reflux into the esophagus.

How is gastrostomy tube cared for?
It is easy to care for the tube at home. Just remember to flush it well after every use with water. Some recommend using any carbonated drink (any soda drink) to flush the tube because such drinks make lots of bubbles that help clear the tube. If the tube is used to administer crushed tablets, they must be pulverized well before administration and the tube scrupulously irrigated after  use. A clogged tube, if unsalvageable, should be replaced.

How long can a gastrostomy tube be worn and how is it cared for?
A patient’s condition and their health-care provider’s opinion will decide when to stop using a gastrostomy tube. Removing the tube is easy. This can be done by a home health care provider or at the hospital. Typically, the holes in the stomach and skin seal in 48 hours after removing the tube.

Aneurysm of the aorta. Ken U. Ekechukwu, MD, MPH, FACP.

What is aorta?
The aorta is the large artery that carries blood from the heart and distributes it to the rest of the body. The portion of the artery in the chest is called the thoracic aorta, while the portion in the abdomen or belly is the abdominal aorta. In the chest and abdomen the aorta lies behind other viscera, next to the vertebral column. It is the largest artery in the body, measuring about 3 cm in the chest and 2.5 cm in the abdomen, but these measurements vary with sex and age, being larger in men and the elderly.

What is aneurysm?
All arteries in the body have three layers: the innermost layer (tunica intima) is in contact with blood and elastic; the middle layer (tunica media) is mainly composed of smooth muscle and supporting tissue; and the outermost layer (tunica externa or adventitia) is composed of fibrous tissue. These layers, together, keep blood inside an artery and propel it forward.  Weakness in the wall of an artery causes abnormal widening of the artery, an aneurysm (Gr. aneurysma, a widening). Any artery in the body can develop an aneurysm (brain, heart, lung, aorta, liver, kidney, spleen, etc.), but this discussion is about aneurysms of the aorta. A true aneurysm occurs when weakness of all three layers of an artery enlarges the artery by 50% or more of its normal diameter. When such weakness affects fewer than all three layers, the resulting local bulge is called a pseudoaneurysm (pseudo means false). This writing is on true aneurysms not caused by infection.

Why do aneurysms occur?
There are many reasons why true aneurysms occur: some genetic abnormalities that run in families, infections of an artery (bacterial, viral, fungal), autoimmune diseases that cause systemic inflammations that involve the arteries, hypertension, smoking, hypercholesterolemia, diabetes mellitus, and trauma, to name a few.

Why should I be concerned about aortic aneurysms?
The primary concern in all aneurysms is the risk of sudden rupture, which can be catastrophic. The risk of death is high and morbidity is gruesome. The situation is even grimmer when you recognize that most aneurysms grow quietly until they rupture, explaining why most aneurysms of the aorta come to attention serendipitously during investigation for other problems. But now, you can be screened for the disease if you are of the right age and your risk profile fits. Please speak to your health care provider. The risk of rupture rises as an aneurysm grows, taking a steep climb when an aneurysm of the ascending aorta attains 6 cm in diameter or an aneurysm of the descending thoracic aorta or the abdominal aorta is 5 cm in diameter. This explains why current standard-of-care recommends treating these aneurysms when they attain these measurements.

How do I know that I have an aortic aneurysm?
There is a good chance that you may not know that you have an aortic aneurysm. If, however, you have risks for the disease it is good to speak to your healthcare provider. Such risks include a family history of aneurysms, smoking, hypertension, hypercholesterolemia, and diabetes mellitus.

Is there treatment for aortic aneurysms?
First, not all aneurysms need immediate attention. Chest and abdominal aortic aneurysms need to grow to the right size to demand fixing. So, if your aneurysm is still ‘a baby aneurysm’ and not the result of an infection, your health care provider may elect to watch it and control your blood pressure and other health problems with medications.  More important is taking steps on your own to prevent the development of an aneurysm including avoiding the use of tobacco. Aneurysms that have grown to treatable sizes may be addressed surgically or endovascularly.

Endovascular repair of an abdominal or thoracic aneurysm is a minimally invasive therapy performed by interventional radiologists and other vascular specialists. It requires the insertion of a special kind of stent called a stent-graft across the dilated part of the aorta to reinforce the wall and separate (actually, protect) it from the forces of blood pulsation. It is reasonably safe and effective in capable hands and requires a short hospital stay, barring unexpected outcomes. Most patients who receive endovascular repair of an aortic aneurysm return to normal activities within 2 weeks. The treatment is not offered to every patient with aortic aneurysm, because certain structural characteristics of the aneurysm may forbid endovascular repair.

Central venous access. Ken U. Ekechukwu, MD, MPH, FACP.

What is a central venous access?
A central venous access (a.k.a. a central line  or a central venous catheter) is a catheter placed into a patient and its tip advanced into a central vein. The right atrium, the superior and inferior vena cava, the subclavian veins, the brachiocephalic veins and the iliac veins are considered central veins.

Because large volumes of blood pass through these chambers or vessels per unit time, medications or nutrients, which are weak acids and bases with variable potential for damaging the venous wall, are quickly diluted and ‘flushed’ on when injected directly into the central veins. When they are used for hemodialysis, the capacity of these vessels is adequate for the high flow rates necessary for efficient dialysis and avoids the venturi effect that sucks venous wall into the catheter side holes and impedes dialysis.

The location of the vein where the catheter enters the body before journeying to the heart modifies its name. Thus, venous access through the jugular, subclavian, or femoral vein or the inferior vena cava is a centrally inserted central venous access (CICVA) or centrally inserted central catheter (CICC); when the insertion site is the cephalic or basilic vein or a deep vein of the arm, the access is called a peripherally inserted central catheter (PICC).

What happens to the trailing end of the catheter is equally important.  It may be secured to the skin where it enters the vein and called a non-tunneled venous access, or burrowed beneath the skin for a variable distance before exiting unto the surface as a tunneled venous access.

The trailing end of the tunneled catheter may be attached to a hub and secured to the skin with sutures or other chic fasteners, and is called a tunneled catheter without a subcutaneous port, or connected to a reservoir (port) buried in a pocket fashioned beneath the skin, and is called a tunneled catheter with a subcutaneous port. (A port is a small hollow round container made with metal or plastic material and covered with rubber-like diaphragm. A small spout leads from its bottom and is the attachment for the catheter.) At use the subcutaneous port’s diaphragm is pierced through the skin ( this is called ‘accessing’) with a special non-coring needle called a Huber needle. A non-coring needle is preferred over other forms of needle because it does not destroy the diaphragm of the reservoir over time, whereas other needles chip it away over time allowing injectants to leak through it. The shaft of the tunneled catheter unattached to a port or pump is fitted with a cuff of collagen that reacts with the tissues beneath the skin to form a firm and durable bond that keeps the catheter from falling out.

The advantages of tunneled central venous accesses over non-tunneled accesses include less risk of infection, enhanced durability, and less risk of accidental or spontaneous explantation. Tunneled catheters attached to subcutaneous ports have the additional value of aesthetics: only the patient knows they exist because they are hidden by the skin.

Each of these catheters comes as a single-lumen or a double-lumen catheter and is usually ready for use immediately after its placement.

Who needs a central venous access?
In a general sense, if you need prolonged access into your veins for the administration of medications, fluids, or nutrients or frequent withdrawal of blood from you for various tests, it makes good sense to place a durable venous access in you early in your care, not after many days of needle sticks for the same purposes. Sometimes, however, the right time for such an intervention is unclear upon your admission to the hospital, but the earlier the decision is made the better it is for you. There are situations we know will invariably require long-lasting central venous access and they include hemodialysis for end-stage kidney failure; chemotherapy for various cancers; difficult-to-stick patients like those who have lost their veins through chronic injection of illicit drugs or those whose chronic ill-health has caused them their veins from frequent needle sticks like people with sickle cell disease.

Non-tunneled catheters are usable for up to three (3) months, if cared for well. Tunneled catheters can stay in patients even longer and are usually placed in those with chronic conditions that require prolonged venous access such as those on hemodialysis for kidney failure, or in patients whose treatment for their disease requires many cycles of intravenous injections.

Preparing for the placement of a central venous access
You do not need any special preparation for the placement of these lines or accesses, except perhaps the tunneled accesses. Many operators provide local anesthesia for the placement of a PICC line, whereas the placement of a tunneled access generally requires deep sedation, usually with a combination of an opiate and a benzodiazepine; such placement takes a slightly longer time and is a little more involved. For these reasons, standard of care requires that you avoid eating or drinking at least 8 hours prior to the procedure to prevent aspiration of your gastric contents into your lungs, because you lose your  protective airway reflexes in deep sedation. It is important to prepare yourself mentally for the procedure.

How is a central venous access placed?
The method of placing a central venous access varies from operator to operator. In general, however, the technique requires strict attention to detail to reduce the risk of infection.  Some institutions place PICCs at patients’ bedside, while others place all central venous accesses in a more controlled environment like an interventional radiology or surgical suite.

After receiving local anesthetic with or without deep sedation, the operator will identify and access a vein in the arm, the root of the neck, or the groin (depending on the patient’s condition, needs, and patency of veins, or the operator’s preference), guided by anatomic landmarks, palpation, or an imaging modality like ultrasound and fluoroscopy; fluoroscopy requires the injection of radiocontrast (dye) into a peripheral vein to opacify the veins in the arm. Then the catheter is introduced into the punctured vein and advanced centrally towards the heart. The hub of the catheter is then secured to the patient’s skin with sutures or, in the case of tunneled catheters, its trailing end is tunneled subcutaneously away from the venous puncture site and attached to a pump or port or is fitted with a hub.

What can go wrong during and after the placement of a central venous access?
The placement of a central venous access is relatively safe, but it is good to be aware of the following things that may go wrong:
1. The skin site may become infected several days, weeks, or months after the catheter placement or a system-wide infection may develop, also after a variable time.
2. The closeness of the tip of the catheter to the lining of heart chambers (the endocardium) may precipitate an infection of the lining (endocarditis) that evolves into a system-wide infection.
3. During the placement of the catheter a near-by artery or nerve may be unintentionally injured.
4. If the venous access is at the root of the neck or close to the chest wall, a patient may sustain a pneumothorax (the accumulation of air within the potential space around the lung) or hemothorax (the accumulation of blood within the potential space around the lung) from injury to the pleura (the covering membrane of the lung) or a nearby blood vessel or both. These two complications may develop rapidly or slowly and may threaten life if not detected and managed early.
5. The vein through which the catheter passes to the heart may thrombose (occlude with clot) and cause arm or neck swelling.
6. Rarely, patients suck air into their blood stream through the instruments used for the procedure. The sucking in of a small amount of air may be tolerated by the patient, but larger amounts may be catastrophic.

What are the contraindications to the placement of a central venous access?
There are not many contraindications to the placement of a central venous access, but the following apply:
1. The presence of systemic infection, which means whole-body infection.
2. The presence of severe coagulopathy (significant ‘thinning’ of the blood) that may cause the patient to bleed excessively during or after the procedure.
3. Lack of suitable veins.
4. If the patient does not want the procedure.

How to care for a central venous access
If the need for your access is immediate, you can use it right after its placement. You will be sore at the site of the procedure for a few days, but will do well with analgesics like acetaminophen (Tylenol). For the first few days keep your wound dry and clean and be in touch with your care giver. In some IR practices an IR nurse will call you within 24 hours of your procedure to check how you are doing. If the operator used non-absorbable sutures (these are made from materials that your body will not absorb over time) to close your wound, be sure he tells you when to return for their removal. Finally, keep a watchful eye on the catheter site and yourself and do not delay reporting to your provider early signs of local or system-wide infection such as new or persistent pain and redness at the wound site, seepage of foul fluid from the skin entry site, fever, chills, or a sense of not feeling well (malaise).

How long can a central venous access be used and how is it removed?
Excluding those catheters that are hurriedly placed in sick patients in the intensive care unit or the emergency department as part of the urgent life-saving measures that swirl around them at the beginning of the ill-health and are usually removed or changed within 7 days, most central venous accesses are durable. Some, like the dialysis catheter, may remain in the patient for years, if their condition demands continuous use of the catheter.  Others are kept in for a few months. Most are removed from the patient when the need for them no longer exists because they are foreign bodies and potential nidus for setting up infection. The non-tunneled catheters are easily pulled out and bleeding at the insertion site controlled by a brief application of pressure. Removal of tunneled catheters requires dissecting them out through small skin incisions and generally is done in the interventional radiology suite or the operating room. The procedure is much quicker and a less harrowing emotional experience than the placement of the catheter.

 

Percutaneous aspiration or drainage of body fluids. Ken U. Ekechukwu, MD, MPH, FACP.

What are body fluids?
Blood is body fluid, but a natural one and so is cerebrospinal fluid which baths the brain and the spinal cord. There are, however, times when ill-health in specific parts of the body induce the formation of abnormal collections of fluid, which if not diagnosed and drained will cause more problems. Abscesses from infections, ascites from a failed liver, heart, or kidney, and hydrothorax from a lung infection, lung cancer, or heart failure are a few of such instances. Commonly, your health care provider decides when a body fluid needs to sampled for diagnosis or drained for treatment. What is percutaneous aspiration or drainage? There was a time in the history of medicine when the removal of most serious body fluids like abscesses required a surgeon’s knife and a large gaping wound thereafter that took several weeks to heal and left an ugly scar. Such occasions are now rare, at least in the western hemisphere. This is because interventional radiologists, guided by using such things as fluoroscopy (x-rays), ultrasound, and CT scan can easily ‘see’ and remove these fluids, usually by passing small tubes called drainage catheters through small cuts (less than 2 mm wide) they make in the skin. Per (through) cutaneous (derived from cutis which means skin) drainage (removal or evacuation) of body fluid, therefore, means draining or removing a body fluid through a skin incision.

What is the preparation for percutaneous imaging-guided aspiration/drainage?
First, you or a designee must ask of and receive from your care provider an account of the merits and demerits of this procedure and its alternatives. When you have done this, you must endorse the procedure by appending your signature on a document called a consent form. A few more details:
1. Understand that this is not major surgery.
2. You will be checked for abnormalities of your clotting system to prevent bleeding complications.
3. Many interventional radiologists perform this procedure with local anesthetics only; you may not need to starve before the procedure.
4. Understand that some body fluids resolve slowly, which means that you may be required to wear the drainage catheter hanging down your side for a short period of time.
5. You may be required to flush the tube periodically if you wear it home. Be sure you clarify this before leaving the hospital or clinic.

How is percutaneous imaging-guided fluid aspiration/drainage done?
If only a small amount of fluid is required for diagnosis, you may have this done as an outpatient procedure, which means you get to go home soon after the procedure. If catheter insertion is necessary, it is usually prudent to remain in the hospital until your provider thinks you can go home. Some infected body fluids require that you receive systemic antibiotic before they are drained to minimize your risk of seeding your blood with the germs responsible for the fluid collection. Usually, previous tests will have determined the location and nature of the body fluid. The operator, after confirming the location of the fluid, will clean the overlying skin with antiseptic agent and isolate it with a sterile drape.

After applying local anesthetic to the skin and the deep tissues, he will make a small skin cut and, through the cut advance a drainage catheter or needle (depending on whether a drainage or aspiration is intended) into the fluid collection. Some body fluids like abscesses can be actively aspirated dry upon catheter insertion, while others, like massive ascites and hydrothorax, are drained more slowly because overzealous and aggressive drainage of such fluids can cause harm. So, whether your fluid will be drained dry upon catheter insertion or allowed to drain slowly will depend on its nature and size.

Thick fluid collections will require periodic flushing of the drainage catheter to dislodge debris that otherwise will clog the holes in the catheters; you or a loved one may have to do this at home.

Who needs imaging-guided aspiration/drainage of body fluid?
• People with large fluid accumulations that cause fever, pain, or discomfort
• Fluid accumulations of unknown cause or source.

What are the contraindications to percutaneous imaging-guided aspiration/drainage of body fluid?
Contraindications are conditions you may have that will make percutaneous fluid drainage hazardous to you. You must let your health care giver know of them before embarking on this procedure. They include:
• Uncorrectable coagulopathy (this means ‘thinning’ of your blood which may make you bleed too much), 
• No safe route (if past surgery or injury left you with scars on and around the drainage site) to the fluid.  How will I care for the tube? It is easy to care for the tube at home by yourself or a loved one. Just remember to flush it regularly (every 6 to 8 hours depending on the thickness and nature of the fluid collection) with sterile water or normal saline. If you are in the hospital your nurses will take care of this for you. How long will I wear the tube and how do I get rid of it when I’m done? Your condition and your health care provider will decide when you will stop wearing the tube. Removing it is easy. You can be taught how to remove it or, when you are done using it, call or visit your care provider at his clinic to remove it. Usually, the hole in the skin seals in 48 hours after removing the tube.

Uterine fibroid (artery) embolization. Ken U. Ekechukwu, MD, MPH, FACP.

What is uterine fibroid embolization?
Uterine fibroids are benign tumors (noncancerous) that grow in the uterus. There may be one or countless fibroids and they grow in any part of the uterus, frequently disfiguring it and making it grow to enormous proportions. These tumors grow and multiply under the influence of the female hormone, estrogen, which explains why they are commoner in women of child-bearing age and begin to shrivel at menopause (except in menopausal women who take hormonal replacement therapy, who may remain symptomatic from fibroids). They occur in women of all races, but are commoner in African American women and nulliparous and low-parity women.

Many women are unaware that they have fibroids because not all fibroids cause symptoms. Symptomatic women may complain of one or several of the following:
1. Heavy, irregular, and prolonged menstrual blood loss that leads to anemia over time.
2. Anemia causes many symptoms and may behave like many other diseases (Easy fatigability, exercise intolerance, dizziness, shortness of breathe, palpitations, etc.).
3. Fibroids can press on nerves in the pelvis and cause radiating pain in the legs.
4. If the womb is large enough it may result in frequent urges to urinate or cause constipation.
5. Sex and menstruation may become painful.
6. When sufficiently large the womb may bulge the abdomen.

Troublesome fibroids (symptomatic fibroids) bring a woman to her doctor’s attention; the quiet ones do not. Most of the women who seek help do so because of heavy and irregular menstruation.

There are several treatment options for symptomatic fibroids: oral contraceptive pills, hormonal injections, myomectomy (the ‘shelling’ out of fibroids), hysterectomy, thermal ablation, and uterine artery embolization. Each has its merits and demerits and the reader is encouraged to consult their health care provider for what these are.

Uterine fibroid embolization is the stopping of blood flow into the uterus by injecting embolic agents into the uterine arteries. Embolic agents are floating particles of finite sizes composed of biocompatible materials. These particles plug blood vessels whose sizes match theirs and prevent blood and nutrients from reaching tissues beyond the obstruction causing tissue death. Since fibroids receive more blood flow than the rest of the womb, they get the bulk of these particles and the lack of nourishment causes them to die and involute (shrink). 8 to 9.5 women out of 10 women with symptomatic uterine fibroids who undergo UFE for heavy bleeding report dramatic cessation of their problem or sufficient reduction in the amount of their monthly blood loss that pleases them. This statistic may not hold true if the reason for heavy menstrual loss is a disease other than fibroids. Sometimes such disease co-exists with uterine fibroids and alters the statistic as well. A good example is when uterine adenomyosis co-exists with uterine fibroids and contributes to a woman’s menstrual disorder, a situation that I have found in my experience forecasts a reasonable chance failure of UFE to control the menstrual anomaly. Thus, it is wise to exclude other uterine diseases that cause abnormal menses before proceeding with UFE/UAE, so that the patient and her physician are well prepared for any persistence of symptoms after the treatment; this information has made many a woman decline UFE/UAE in my practice.

How is UFE/UAE done and what should I expect after it?
UFE is not major surgery, rather, like many interventional radiological procedures, it requires little invasion of the body. It is performed in an interventional radiology suite because it requires the use of fluoroscopy (x-rays) for guidance.  It is performed with attention to asepsis and under conscious sedation using a combination of an opiate and a benzodiazepine. The operator finds the arteries that supply your uterus by passing a catheter (a small tube, about the size of uncooked spaghetti) through the artery in one or both groins or the artery in your left arm, using the flow of the radiocontrast (iodine dye) which he injects through the catheter as a road-map. Once he confirms that the tip of the catheter is at the right place in the right vessel, he injects the embolic agent until blood flow into the womb ceases or is significantly reduced.

You will then receive treatment for symptoms caused by the dying fibroids – nausea, vomiting, diminished appetite, abdominal pain, low-grade fever, and a general sense of feeling unwell – collectively called ‘post embolization syndrome’. These symptoms vary in intensity from patient to patient and in most women respond to supportive care; they last from 3 days to 3 weeks. Most of my patients feel well enough the next day to go home; a few have gone home the same day.  They receive prescriptions for medicines to control pain, relieve nausea, prevent infection, and soften their stools and a majority are ready to return to work or resume normal activities in a little over 1 week.

Most patients report passing thin darkish vaginal flow for a few days after their UFE; some resume normal menses after a few months of amenorrhea; others report amenorrhea for many months that merges into menopause; some in a few weeks or several months after the treatment call to report spontaneously passing meaty materials in the toilet bowl, which are fragments of disintegrating fibroids; and yet a very few report lack of change in their initial complaint. Post-UFE experience in my practice varies and I have successfully dealt with it by reassuring and counseling each patient when the frantic call comes. Practically, all show on their follow-up pelvic MRIs variable degrees of reduction in the volume of the uterus and evidence of devascularization and death of the fibroids. Dead fibroids never recur but new ones may develop and grow if the woman is young enough.

How do I prepare for UFE/UAE?
In addition to making necessary arrangements for your absence from home and work, you should prepare yourself mentally and emotionally for UFE. In truth, however, there is not much to fret over for the procedure, particularly if you have researched the procedure well and have had reassuring discussions with your physician. By now you should have completed the investigations necessary for undergoing the procedure: endometrial biopsy (if necessary) to exclude uterine cancer as reason for the bleeding problem; magnetic resonance imaging of your pelvis with intravenous administration of a gadolinium chelate which documents the state of the uterus, the endometrium, the ovaries, your pelvic and gonadal veins and your bone marrow; and blood work to assess your renal function, the severity of your anemia, and your likelihood of bleeding excessively during the procedure. Since you are likely to receive conscious sedation, it is wise to refrain from eating and drinking 6 to 8 hours prior to your procedure.

Who needs UFE/UAE and what are its contraindications?
If you have asymptomatic fibroids (fibroids that do not cause you symptoms) you do not have to have UFE or other treatment for them.

Some women ask to have UFE because they wish to lose weight. Well, although the return to normal size of a womb massively enlarged and grotesquely distorted by many fibroids is likely to come with some weight loss, this is likely to be marginal and will happen slowly over time. Remember that the fibroids do not evaporate into thin air over night after UFE; they took time to grow and will take time to shrink. So I do not flash the image of rapid weight loss as an inviting wand of promise to women seeking UFE for that purpose.

Many young women have symptomatic uterine fibroids and wish to keep their wombs because they are not yet done with having children or have not had any yet. They wish to know the likelihood of becoming pregnant after UFE. The jury is still out on this issue and I do not promise my patients the reward of improved fecundity after UFE. I know, however, that many women have become pregnant after UFE, carried their fetuses to term, and birthed uneventfully. I have had a few in my practice.

Perhaps UFE is best for the woman who is approaching menopause but saddled with the problem of torrential or difficult menstrual blood loss. Since we know that menopause will usher in relief of her symptoms, UFE, instead of hysterectomy, for her problem seems wiser given its simplicity; here UFE serves a bridging role into menopause.

The uterine arteries may be embolized for many other uterine bleeding problems, for instance, post-partum hemorrhage and adenomyosis of the uterus. However, the success rate of UAE for stopping bleeding due to adenomyosis in my experience is much lower than it is for symptomatic uterine fibroids (vide supra). Adenomyosis may coexist with fibroids, which is one other reason I obtain MRI of the pelvis for all my patients. It is prudent for the patient and the physician to be aware of the likelihood of treatment failure before embarking on applying UAE for adenomyosis. My approach to this issue is to present the facts to the patient, help her understand that hysterectomy may be used as a fall-back alternative in the event of UAE failure, and let her decide what option to choose.

Abnormal uterine or vaginal bleeding in a menopausal woman should not be treated with UFE, but investigated and its reason determined. Such bleeding may be ominous.

What are the complications of UFE/UAE?
The risks or complications of UFE are few. Since it is done with conscious sedation, the risks associated with general anesthesia do not exist. Since there are no major incisions, the risks associated with wound infection are absent, although the uterus may become infected after embolization. This is preventable and treatable with antibiotics. There may be complications at the puncture site (bleeding, hematoma, infection, finger numbness or paresthesia), all of which are rare, preventable, and treatable.  Another rare and preventable complication is the unintentional flow of the embolization particles to other arteries resulting in tissue ischemia or infarction. Minor non-target embolization of a well-vascularized area may not cause major problems, whereas more serious occurrence may be problematic and is best avoided by attention to embolization technique.